Owen A Ross (Owen Ross)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 59

Top Venues

Movement disorders : official journal of the Movement Disorder Society

Nature genetics

Annals of neurology

Sleep

Mayo Clinic

University of Ulster (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Mayo Clinic

United States

Associate Professor :: Neuroscience

Education History

University of Ulster

Ireland

PHD :: Genetics

Queens University Belfast School of Biological Sciences

Ireland

MSC :: Genetics

Queens University Belfast School of Biological Sciences

Ireland

BSC :: Biochemistry

Publications

Paul J Hop, Dongbing Lai, Pamela J Keagle, Desiree M Baron, Brendan J Kenna, Maarten Kooyman, null Shankaracharya, Cheryl Halter, Letizia Straniero, Rosanna Asselta, Salvatore Bonvegna, Alexandra I Soto-Beasley, null null, Zbigniew K Wszolek, Ryan J Uitti, Ioannis Ugo Isaias, Gianni Pezzoli, Nicola Ticozzi, Owen A Ross, Jan Herman Veldink, Tatiana M Foroud, Kevin P Kenna, John E Landers
Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson's disease. Nature genetics (2024)
Barbara Schormair, Chen Zhao, Steven Bell, Maria Didriksen, Muhammad S Nawaz, Nathalie Schandra, Ambra Stefani, Birgit Högl, Yves Dauvilliers, Cornelius G Bachmann, David Kemlink, Karel Sonka, Walter Paulus, Claudia Trenkwalder, Wolfgang H Oertel, Magdolna Hornyak, Maris Teder-Laving, Andres Metspalu, Georgios M Hadjigeorgiou, Olli Polo, Ingo Fietze, Owen A Ross, Zbigniew K Wszolek, Abubaker Ibrahim, Melanie Bergmann, Volker Kittke, Philip Harrer, Joseph Dowsett, Sofiene Chenini, Sisse Rye Ostrowski, Erik Sørensen, Christian Erikstrup, Ole Birger Vesterager Pedersen, Mie Topholm Bruun, Kaspar R Nielsen, Adam S Butterworth, Nicole Soranzo, Willem Hendrik Ouwehand, David J Roberts, John Danesh, Brendan Burchell, Nicholas A Furlotte, Priyanka Nandakumar, null null, null null, Christopher J Earley, William G Ondo, Lan Xiong, Alex Desautels, Markus Perola, Pavel Vodicka, Christian Dina, Monika Stoll, Andre Franke, Wolfgang Lieb, Alexandre F R Stewart, Svati H Shah, Christian Gieger, Annette Peters, David B Rye, Guy A Rouleau, Klaus Berger, Hreinn Stefansson, Henrik Ullum, Kari Stefansson, David A Hinds, Emanuele Di Angelantonio, Konrad Oexle, Juliane Winkelmann
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction. Nature genetics 56 (6) (2024)
Barbara Schormair, Chen Zhao, Steven Bell, Maria Didriksen, Muhammad S Nawaz, Nathalie Schandra, Ambra Stefani, Birgit Högl, Yves Dauvilliers, Cornelius G Bachmann, David Kemlink, Karel Sonka, Walter Paulus, Claudia Trenkwalder, Wolfgang H Oertel, Magdolna Hornyak, Maris Teder-Laving, Andres Metspalu, Georgios M Hadjigeorgiou, Olli Polo, Ingo Fietze, Owen A Ross, Zbigniew K Wszolek, Abubaker Ibrahim, Melanie Bergmann, Volker Kittke, Philip Harrer, Joseph Dowsett, Sofiene Chenini, Sisse Rye Ostrowski, Erik Sørensen, Christian Erikstrup, Ole Birger Vesterager Pedersen, Mie Topholm Bruun, Kaspar R Nielsen, Adam S Butterworth, Nicole Soranzo, Willem Hendrik Ouwehand, David J Roberts, John Danesh, Brendan Burchell, Nicholas A Furlotte, Priyanka Nandakumar, null null, null null, Christopher J Earley, William G Ondo, Lan Xiong, Alex Desautels, Markus Perola, Pavel Vodicka, Christian Dina, Monika Stoll, Andre Franke, Wolfgang Lieb, Alexandre F R Stewart, Svati H Shah, Christian Gieger, Annette Peters, David B Rye, Guy A Rouleau, Klaus Berger, Hreinn Stefansson, Henrik Ullum, Kari Stefansson, David A Hinds, Emanuele Di Angelantonio, Konrad Oexle, Juliane Winkelmann
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction. Nature genetics (2024)
Barbara Schormair, Chen Zhao, Steven Bell, Maria Didriksen, Muhammad S Nawaz, Nathalie Schandra, Ambra Stefani, Birgit Högl, Yves Dauvilliers, Cornelius G Bachmann, David Kemlink, Karel Sonka, Walter Paulus, Claudia Trenkwalder, Wolfgang H Oertel, Magdolna Hornyak, Maris Teder-Laving, Andres Metspalu, Georgios M Hadjigeorgiou, Olli Polo, Ingo Fietze, Owen A Ross, Zbigniew K Wszolek, Abubaker Ibrahim, Melanie Bergmann, Volker Kittke, Philip Harrer, Joseph Dowsett, Sofiene Chenini, Sisse Rye Ostrowski, Erik Sørensen, Christian Erikstrup, Ole Birger Vesterager Pedersen, Mie Topholm Bruun, Kaspar R Nielsen, Adam S Butterworth, Nicole Soranzo, Willem Hendrik Ouwehand, David J Roberts, John Danesh, Brendan Burchell, Nicholas A Furlotte, Priyanka Nandakumar, null null, null null, Christopher J Earley, William G Ondo, Lan Xiong, Alex Desautels, Markus Perola, Pavel Vodicka, Christian Dina, Monika Stoll, Andre Franke, Wolfgang Lieb, Alexandre F R Stewart, Svati H Shah, Christian Gieger, Annette Peters, David B Rye, Guy A Rouleau, Klaus Berger, Hreinn Stefansson, Henrik Ullum, Kari Stefansson, David A Hinds, Emanuele Di Angelantonio, Konrad Oexle, Juliane Winkelmann
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction. Nature genetics 56 (6) (2024)
Barbara Schormair, Chen Zhao, Steven Bell, Maria Didriksen, Muhammad S Nawaz, Nathalie Schandra, Ambra Stefani, Birgit Högl, Yves Dauvilliers, Cornelius G Bachmann, David Kemlink, Karel Sonka, Walter Paulus, Claudia Trenkwalder, Wolfgang H Oertel, Magdolna Hornyak, Maris Teder-Laving, Andres Metspalu, Georgios M Hadjigeorgiou, Olli Polo, Ingo Fietze, Owen A Ross, Zbigniew K Wszolek, Abubaker Ibrahim, Melanie Bergmann, Volker Kittke, Philip Harrer, Joseph Dowsett, Sofiene Chenini, Sisse Rye Ostrowski, Erik Sørensen, Christian Erikstrup, Ole Birger Vesterager Pedersen, Mie Topholm Bruun, Kaspar R Nielsen, Adam S Butterworth, Nicole Soranzo, Willem Hendrik Ouwehand, David J Roberts, John Danesh, Brendan Burchell, Nicholas A Furlotte, Priyanka Nandakumar, null null, null null, Christopher J Earley, William G Ondo, Lan Xiong, Alex Desautels, Markus Perola, Pavel Vodicka, Christian Dina, Monika Stoll, Andre Franke, Wolfgang Lieb, Alexandre F R Stewart, Svati H Shah, Christian Gieger, Annette Peters, David B Rye, Guy A Rouleau, Klaus Berger, Hreinn Stefansson, Henrik Ullum, Kari Stefansson, David A Hinds, Emanuele Di Angelantonio, Konrad Oexle, Juliane Winkelmann
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction. Nature genetics 56 (6) (2024)
Paul J Hop, Dongbing Lai, Pamela J Keagle, Desiree M Baron, Brendan J Kenna, Maarten Kooyman, null Shankaracharya, Cheryl Halter, Letizia Straniero, Rosanna Asselta, Salvatore Bonvegna, Alexandra I Soto-Beasley, null null, Zbigniew K Wszolek, Ryan J Uitti, Ioannis Ugo Isaias, Gianni Pezzoli, Nicola Ticozzi, Owen A Ross, Jan Herman Veldink, Tatiana M Foroud, Kevin P Kenna, John E Landers
Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson's disease. Nature genetics 56 (7) (2024)
Kurt Farrell, Jack Humphrey, Timothy S Chang, Yi Zhao, Yuk Yee Leung, Pavel P Kuksa, Vishakha Patil, Wan-Ping Lee, Amanda B Kuzma, Otto Valladares, Laura B Cantwell, Hui Wang, Ashvin Ravi, Claudia De Sanctis, Natalia Han, Thomas D Christie, Robina Afzal, Shrishtee Kandoi, Kristen Whitney, Margaret M Krassner, Hadley Ressler, SoongHo Kim, Diana Dangoor, Megan A Iida, Alicia Casella, Ruth H Walker, Melissa J Nirenberg, Alan E Renton, Bergan Babrowicz, Giovanni Coppola, Towfique Raj, Günter U Höglinger, Ulrich Müller, Lawrence I Golbe, Huw R Morris, John Hardy, Tamas Revesz, Thomas Treharne Warner, Zane T Jaunmuktane, Kin Y Mok, Rosa Rademakers, Gourisankar Ghosh, Owen A Ross, Li-San Wang, Alison Mary Goate, Gerard Schellenberg, Daniel H Geschwind, null null, John F Crary, Adam C Naj
Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genes. Nature communications 15 (1) (2024)
Adriana Vázquez-Medina, Marion T Turnbull, Courtney L James, Jennifer B Cowart, Elizabeth Lesser, Rickey E Carter, Owen A Ross, David A Miller, James F Meschia, Aixa De Jesús Espinosa, Richard Weinshilboum, William David Freeman
Nimodipine-associated standard dose reductions and neurologic outcomes after aneurysmal subarachnoid hemorrhage: the era of pharmacogenomics. The pharmacogenomics journal 24 (4) (2024)
Jonathan E Elliott, Brittany R Ligman, Mohini D Bryant-Ekstrand, Allison T Keil, Katherine Powers, Cosette Olivo, Lee E Neilson, Ronald B Postuma, Amélie Pelletier, Jean-François Gagnon, Ziv Gan Or, Eric Yu, Lang Liu, Erik K St Louis, Leah K Forsberg, Julie A Fields, Owen A Ross, Daniel E Huddleston, Donald L Bliwise, Alon Y Avidan, Michael J Howell, Carlos H Schenck, Jennifer McLeland, Susan R Criswell, Aleksandar Videnovic, Emmanuel H During, Mitchell G Miglis, David R Shprecher, Joyce K Lee-Iannotti, Bradley F Boeve, Yo-El S Ju, Miranda M Lim, null null
Comorbid neurotrauma increases neurodegenerative-relevant cognitive, motor, and autonomic dysfunction in patients with rapid eye movement sleep behavior disorder: a substudy of the North American Prodromal Synucleinopathy Consortium. Sleep 47 (6) (2024)
Nathaniel B Gunter, Robel K Gebre, Jonathan Graff-Radford, Michael G Heckman, Clifford R Jack, Val J Lowe, David S Knopman, Ronald C Petersen, Owen A Ross, Prashanthi Vemuri, Vijay K Ramanan, null null
Machine Learning Models of Polygenic Risk for Enhanced Prediction of Alzheimer Disease Endophenotypes. Neurology. Genetics 10 (1) (2024)
Jonathan E Elliott, Brittany R Ligman, Mohini D Bryant-Ekstrand, Allison T Keil, Katherine Powers, Cosette Olivo, Lee E Neilson, Ronald B Postuma, Amélie Pelletier, Jean-François Gagnon, Ziv Gan Or, Eric Yu, Lang Liu, Erik K St Louis, Leah K Forsberg, Julie A Fields, Owen A Ross, Daniel E Huddleston, Donald L Bliwise, Alon Y Avidan, Michael J Howell, Carlos H Schenck, Jennifer McLeland, Susan R Criswell, Aleksandar Videnovic, Emmanuel H During, Mitchell G Miglis, David R Shprecher, Joyce K Lee-Iannotti, Bradley F Boeve, Yo-El S Ju, Miranda M Lim, null null
Comorbid neurotrauma increases neurodegenerative-relevant cognitive, motor, and autonomic dysfunction in patients with rapid eye movement sleep behavior disorder: a substudy of the North American Prodromal Synucleinopathy Consortium. Sleep 47 (6) (2024)
Kimberly C Olney, Benjamin E Rabichow, Aleksandra M Wojtas, Michael DeTure, Pamela J McLean, Gourisankar Ghosh, Rui Chang, Owen A Ross, John D Fryer
Distinct transcriptional alterations distinguish Lewy body disease from Alzheimer's disease. Brain : a journal of neurology (2024)
Nathaniel B Gunter, Robel K Gebre, Jonathan Graff-Radford, Michael G Heckman, Clifford R Jack, Val J Lowe, David S Knopman, Ronald C Petersen, Owen A Ross, Prashanthi Vemuri, Vijay K Ramanan, null null
Machine Learning Models of Polygenic Risk for Enhanced Prediction of Alzheimer Disease Endophenotypes. Neurology. Genetics 10 (1) (2024)
Yuri L Sosero, Sara Bandres-Ciga, Bart Ferwerda, Maria T P Tocino, Dìaz R Belloso, Pilar Gomez-Gil, Johann Faouzi, Pille Taba, Lukas Pavelka, Tainà M Marques, Clarissa P C Gomes, Alexey Kolodkin, Patrick May, Lukasz M Milanowski, Zbigniew K Wszolek, Ryan J Uitti, Peter Heutink, Jacobus J van Hilten, David K Simon, Shirley Eberly, Ignacio Alvarez, Lynne Krohn, Eric Yu, Kathryn Freeman, Uladzislau Rudakou, Jennifer A Ruskey, Farnaz Asayesh, Manuel Menéndez-Gonzàlez, Pau Pastor, Owen A Ross, Rejko Krüger, null null, Jean-Christophe Corvol, Sulev Kõks, Pablo Mir, Rob M A de Bie, Hirotaka Iwaki, Ziv Gan Or, null null
Dopamine Pathway and Parkinson's Risk Variants Are Associated with Levodopa-Induced Dyskinesia. Movement disorders : official journal of the Movement Disorder Society (2024)
Jonathan E Elliott, Brittany R Ligman, Mohini D Bryant-Ekstrand, Allison T Keil, Katherine Powers, Cosette Olivo, Lee E Neilson, Ronald B Postuma, Amélie Pelletier, Jean-François Gagnon, Ziv Gan Or, Eric Yu, Lang Liu, Erik K St Louis, Leah K Forsberg, Julie A Fields, Owen A Ross, Daniel E Huddleston, Donald L Bliwise, Alon Y Avidan, Michael J Howell, Carlos H Schenck, Jennifer McLeland, Susan R Criswell, Aleksandar Videnovic, Emmanuel H During, Mitchell G Miglis, David R Shprecher, Joyce K Lee-Iannotti, Bradley F Boeve, Yo-El S Ju, Miranda M Lim, null null
Comorbid neurotrauma increases neurodegenerative-relevant cognitive, motor, and autonomic dysfunction in patients with REM sleep behavior disorder: A substudy of the North American Prodromal Synucleinopathy Consortium. Sleep (2024)
Jonathan E Elliott, Brittany R Ligman, Mohini D Bryant-Ekstrand, Allison T Keil, Katherine Powers, Cosette Olivo, Lee E Neilson, Ronald B Postuma, Amélie Pelletier, Jean-François Gagnon, Ziv Gan Or, Eric Yu, Lang Liu, Erik K St Louis, Leah K Forsberg, Julie A Fields, Owen A Ross, Daniel E Huddleston, Donald L Bliwise, Alon Y Avidan, Michael J Howell, Carlos H Schenck, Jennifer McLeland, Susan R Criswell, Aleksandar Videnovic, Emmanuel H During, Mitchell G Miglis, David R Shprecher, Joyce K Lee-Iannotti, Bradley F Boeve, Yo-El S Ju, Miranda M Lim, null null
Comorbid neurotrauma increases neurodegenerative-relevant cognitive, motor, and autonomic dysfunction in patients with REM sleep behavior disorder: A substudy of the North American Prodromal Synucleinopathy Consortium. Sleep (2024)
Paul J Hop, Dongbing Lai, Pamela J Keagle, Desiree M Baron, Brendan J Kenna, Maarten Kooyman, null Shankaracharya, Cheryl Halter, Letizia Straniero, Rosanna Asselta, Salvatore Bonvegna, Alexandra I Soto-Beasley, null null, Zbigniew K Wszolek, Ryan J Uitti, Ioannis Ugo Isaias, Gianni Pezzoli, Nicola Ticozzi, Owen A Ross, Jan Herman Veldink, Tatiana M Foroud, Kevin P Kenna, John E Landers
Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson's disease. Nature genetics 56 (7) (2024)
Ronald B Postuma, Nisa Vorasoot, Erik K St Louis, Amélie Pelletier, Miranda M Lim, Jonathan E Elliott, Jean-François Gagnon, Ziv Gan-Or, Leah K Forsberg, Julie A Fields, Owen A Ross, Wolfgang Singer, Daniel E Huddleston, Donald L Bliwise, Alon Y Avidan, Michael J Howell, Carlos H Schenck, Jennifer McLeland, Albert A Davis, Susan R Criswell, Aleksandar Videnovic, Emmanuel H During, Mitchell G Miglis, Bradley F Boeve, Yo-El S Ju, Andrew McKeon, null null
IGLON5 Frequency in Idiopathic REM Sleep Behavior Disorder: A Multicenter Study. Neurology(R) neuroimmunology & neuroinflammation 11 (6) (2024)
Paul J Hop, Dongbing Lai, Pamela J Keagle, Desiree M Baron, Brendan J Kenna, Maarten Kooyman, null Shankaracharya, Cheryl Halter, Letizia Straniero, Rosanna Asselta, Salvatore Bonvegna, Alexandra I Soto-Beasley, null null, Zbigniew K Wszolek, Ryan J Uitti, Ioannis Ugo Isaias, Gianni Pezzoli, Nicola Ticozzi, Owen A Ross, Jan Herman Veldink, Tatiana M Foroud, Kevin P Kenna, John E Landers
Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson's disease. Nature genetics 56 (7) (2024)
Barbara Schormair, Chen Zhao, Steven Bell, Maria Didriksen, Muhammad S Nawaz, Nathalie Schandra, Ambra Stefani, Birgit Högl, Yves Dauvilliers, Cornelius G Bachmann, David Kemlink, Karel Sonka, Walter Paulus, Claudia Trenkwalder, Wolfgang H Oertel, Magdolna Hornyak, Maris Teder-Laving, Andres Metspalu, Georgios M Hadjigeorgiou, Olli Polo, Ingo Fietze, Owen A Ross, Zbigniew K Wszolek, Abubaker Ibrahim, Melanie Bergmann, Volker Kittke, Philip Harrer, Joseph Dowsett, Sofiene Chenini, Sisse Rye Ostrowski, Erik Sørensen, Christian Erikstrup, Ole Birger Vesterager Pedersen, Mie Topholm Bruun, Kaspar R Nielsen, Adam S Butterworth, Nicole Soranzo, Willem Hendrik Ouwehand, David J Roberts, John Danesh, Brendan Burchell, Nicholas A Furlotte, Priyanka Nandakumar, null null, null null, Christopher J Earley, William G Ondo, Lan Xiong, Alex Desautels, Markus Perola, Pavel Vodicka, Christian Dina, Monika Stoll, Andre Franke, Wolfgang Lieb, Alexandre F R Stewart, Svati H Shah, Christian Gieger, Annette Peters, David B Rye, Guy A Rouleau, Klaus Berger, Hreinn Stefansson, Henrik Ullum, Kari Stefansson, David A Hinds, Emanuele Di Angelantonio, Konrad Oexle, Juliane Winkelmann
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction. Nature genetics 56 (6) (2024)
Adriana Vázquez-Medina, Marion T Turnbull, Courtney L James, Jennifer B Cowart, Elizabeth Lesser, Rickey E Carter, Owen A Ross, David A Miller, James F Meschia, Aixa De Jesús Espinosa, Richard Weinshilboum, William David Freeman
Nimodipine-associated standard dose reductions and neurologic outcomes after aneurysmal subarachnoid hemorrhage: the era of pharmacogenomics. The pharmacogenomics journal 24 (4) (2024)
Paul J Hop, Dongbing Lai, Pamela J Keagle, Desiree M Baron, Brendan J Kenna, Maarten Kooyman, null Shankaracharya, Cheryl Halter, Letizia Straniero, Rosanna Asselta, Salvatore Bonvegna, Alexandra I Soto-Beasley, null null, Zbigniew K Wszolek, Ryan J Uitti, Ioannis Ugo Isaias, Gianni Pezzoli, Nicola Ticozzi, Owen A Ross, Jan Herman Veldink, Tatiana M Foroud, Kevin P Kenna, John E Landers
Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson's disease. Nature genetics 56 (7) (2024)
Paul J Hop, Dongbing Lai, Pamela J Keagle, Desiree M Baron, Brendan J Kenna, Maarten Kooyman, null Shankaracharya, Cheryl Halter, Letizia Straniero, Rosanna Asselta, Salvatore Bonvegna, Alexandra I Soto-Beasley, null null, Zbigniew K Wszolek, Ryan J Uitti, Ioannis Ugo Isaias, Gianni Pezzoli, Nicola Ticozzi, Owen A Ross, Jan Herman Veldink, Tatiana M Foroud, Kevin P Kenna, John E Landers
Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson's disease. Nature genetics 56 (7) (2024)
Barbara Schormair, Chen Zhao, Steven Bell, Maria Didriksen, Muhammad S Nawaz, Nathalie Schandra, Ambra Stefani, Birgit Högl, Yves Dauvilliers, Cornelius G Bachmann, David Kemlink, Karel Sonka, Walter Paulus, Claudia Trenkwalder, Wolfgang H Oertel, Magdolna Hornyak, Maris Teder-Laving, Andres Metspalu, Georgios M Hadjigeorgiou, Olli Polo, Ingo Fietze, Owen A Ross, Zbigniew K Wszolek, Abubaker Ibrahim, Melanie Bergmann, Volker Kittke, Philip Harrer, Joseph Dowsett, Sofiene Chenini, Sisse Rye Ostrowski, Erik Sørensen, Christian Erikstrup, Ole Birger Vesterager Pedersen, Mie Topholm Bruun, Kaspar R Nielsen, Adam S Butterworth, Nicole Soranzo, Willem Hendrik Ouwehand, David J Roberts, John Danesh, Brendan Burchell, Nicholas A Furlotte, Priyanka Nandakumar, null null, null null, Christopher J Earley, William G Ondo, Lan Xiong, Alex Desautels, Markus Perola, Pavel Vodicka, Christian Dina, Monika Stoll, Andre Franke, Wolfgang Lieb, Alexandre F R Stewart, Svati H Shah, Christian Gieger, Annette Peters, David B Rye, Guy A Rouleau, Klaus Berger, Hreinn Stefansson, Henrik Ullum, Kari Stefansson, David A Hinds, Emanuele Di Angelantonio, Konrad Oexle, Juliane Winkelmann
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction. Nature genetics 56 (6) (2024)
Barbara Schormair, Chen Zhao, Steven Bell, Maria Didriksen, Muhammad S Nawaz, Nathalie Schandra, Ambra Stefani, Birgit Högl, Yves Dauvilliers, Cornelius G Bachmann, David Kemlink, Karel Sonka, Walter Paulus, Claudia Trenkwalder, Wolfgang H Oertel, Magdolna Hornyak, Maris Teder-Laving, Andres Metspalu, Georgios M Hadjigeorgiou, Olli Polo, Ingo Fietze, Owen A Ross, Zbigniew K Wszolek, Abubaker Ibrahim, Melanie Bergmann, Volker Kittke, Philip Harrer, Joseph Dowsett, Sofiene Chenini, Sisse Rye Ostrowski, Erik Sørensen, Christian Erikstrup, Ole Birger Vesterager Pedersen, Mie Topholm Bruun, Kaspar R Nielsen, Adam S Butterworth, Nicole Soranzo, Willem Hendrik Ouwehand, David J Roberts, John Danesh, Brendan Burchell, Nicholas A Furlotte, Priyanka Nandakumar, null null, null null, Christopher J Earley, William G Ondo, Lan Xiong, Alex Desautels, Markus Perola, Pavel Vodicka, Christian Dina, Monika Stoll, Andre Franke, Wolfgang Lieb, Alexandre F R Stewart, Svati H Shah, Christian Gieger, Annette Peters, David B Rye, Guy A Rouleau, Klaus Berger, Hreinn Stefansson, Henrik Ullum, Kari Stefansson, David A Hinds, Emanuele Di Angelantonio, Konrad Oexle, Juliane Winkelmann
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction. Nature genetics 56 (6) (2024)
Yunjung Jin, Fuyao Li, Zonghua Li, Tadafumi C Ikezu, Justin O'Leary, Manikandan Selvaraj, Yiyang Zhu, Yuka A Martens, Shunsuke Koga, Hannah Santhakumar, Yonghe Li, Wenyan Lu, Yang You, Kiara Lolo, Michael A DeTure, Alexandra I Beasley, Mary D Davis, Pamela J McLean, Owen A Ross, Takahisa Kanekiyo, Tsuneya Ikezu, Thomas R Caulfield, Jonathan A Carr, Zbigniew K Wszolek, Guojun Bu, Gourisankar Ghosh, Na Zhao
Modeling Lewy body disease with SNCA triplication iPSC-derived cortical organoids and identifying therapeutic drugs. Science advances 10 (37) (2024)
Yuri L Sosero, Sara Bandres-Ciga, Bart Ferwerda, Maria T P Tocino, Dìaz R Belloso, Pilar Gomez-Gil, Johann Faouzi, Pille Taba, Lukas Pavelka, Tainà M Marques, Clarissa P C Gomes, Alexey Kolodkin, Patrick May, Lukasz M Milanowski, Zbigniew K Wszolek, Ryan J Uitti, Peter Heutink, Jacobus J van Hilten, David K Simon, Shirley Eberly, Ignacio Alvarez, Lynne Krohn, Eric Yu, Kathryn Freeman, Uladzislau Rudakou, Jennifer A Ruskey, Farnaz Asayesh, Manuel Menéndez-Gonzàlez, Pau Pastor, Owen A Ross, Rejko Krüger, null null, Jean-Christophe Corvol, Sulev Kõks, Pablo Mir, Rob M A de Bie, Hirotaka Iwaki, Ziv Gan Or, null null
Dopamine Pathway and Parkinson's Risk Variants Are Associated with Levodopa-Induced Dyskinesia. Movement disorders : official journal of the Movement Disorder Society (2024)
Paul J Hop, Dongbing Lai, Pamela J Keagle, Desiree M Baron, Brendan J Kenna, Maarten Kooyman, null Shankaracharya, Cheryl Halter, Letizia Straniero, Rosanna Asselta, Salvatore Bonvegna, Alexandra I Soto-Beasley, null null, Zbigniew K Wszolek, Ryan J Uitti, Ioannis Ugo Isaias, Gianni Pezzoli, Nicola Ticozzi, Owen A Ross, Jan Herman Veldink, Tatiana M Foroud, Kevin P Kenna, John E Landers
Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson's disease. Nature genetics 56 (7) (2024)
Eva-Juliane Vollstedt, Susen Schaake, Katja Lohmann, Shalini Padmanabhan, Alexis Brice, Suzanne Lesage, Christelle Tesson, Marie Vidailhet, Isabel Wurster, Faycel Hentati, Anat Mirelman, Nir Giladi, Karen Marder, Cheryl Waters, Stanley Fahn, Meike Kasten, Norbert Brüggemann, Max Borsche, Tatiana Foroud, Eduardo Tolosa, Alicia Garrido, Grazia Annesi, Monica Gagliardi, Maria Bozi, Leonidas Stefanis, Joaquim José Ferreira, Leonor Correia Guedes, Micol Avenali, Simona Petrucci, Lorraine Clark, Ekaterina Y Fedotova, Natalya Y Abramycheva, Victoria Alvarez, Manuel Menéndez-González, Silvia Jesús Maestre, Pilar Gómez-Garre, Pablo Mir, Andrea Carmine Belin, Caroline Ran, Chin-Hsien Lin, Ming-Che Kuo, David Crosiers, Zbigniew K Wszolek, Owen A Ross, Joseph Jankovic, Kenya Nishioka, Manabu Funayama, Jordi Clarimon, Caroline H Williams-Gray, Marta Camacho, Mario R Cornejo-Olivas, Luis Torres-Ramirez, Yih-Ru Wu, Guey-Jen Lee-Chen, Ana Morgadinho, Teeratorn Pulkes, Pichet Termsarasab, Daniela Berg, Gregor Kuhlenbäumer, Andrea A Kühn, Friederike Borngräber, Giuseppe de Michele, Anna De Rosa, Alexander Zimprich, Andreas Puschmann, George D Mellick, Jolanta Dorszewska, Jonathan Carr, Rosangela Ferese, Stefano Gambardella, Bruce A Chase, Katerina Markopoulou, Wataru Satake, Tatsushi Toda, Malco Rossi, Marcelo Merello, Timothy Lynch, Diana Angelika Olszewska, Shen-Yang Lim, Azlina Ahmad-Annuar, Ai-Huey Tan, Bashayer Al-Mubarak, Hasmet Hanagasi, Dariusz Koziorowski, Sibel Ertan, Gençer Genç, Patricia de Carvalho Aguiar, Melinda Barkhuizen, Marcia M G Pimentel, Rachel Saunders-Pullman, Bart van de Warrenburg, Susan Bressman, Mathias Toft, Silke Appel-Cresswell, Anthony E Lang, Matej Skorvanek, Agnita J W Boon, Rejko Krüger, Esther M Sammler, Vitor Tumas, Bao-Rong Zhang, Gaetan Garraux, Sun Ju Chung, Yun Joong Kim, Juliane Winkelmann, Carolyn M Sue, Eng-King Tan, Joana Damásio, Péter Klivényi, Vladimir S Kostic, David Arkadir, Mika Martikainen, Vanderci Borges, Jens Michael Hertz, Laura Brighina, Mariana Spitz, Oksana Suchowersky, Olaf Riess, Parimal Das, Brit Mollenhauer, Emilia M Gatto, Maria Skaalum Petersen, Nobutaka Hattori, Ruey-Meei Wu, Sergey N Illarioshkin, Enza Maria Valente, Jan O Aasly, Anna Aasly, Roy N Alcalay, Avner Thaler, Matthew J Farrer, Kathrin Brockmann, Jean-Christophe Corvol, Christine Klein, null null
Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort. Movement disorders : official journal of the Movement Disorder Society (2023)
Eva-Juliane Vollstedt, Susen Schaake, Katja Lohmann, Shalini Padmanabhan, Alexis Brice, Suzanne Lesage, Christelle Tesson, Marie Vidailhet, Isabel Wurster, Faycel Hentati, Anat Mirelman, Nir Giladi, Karen Marder, Cheryl Waters, Stanley Fahn, Meike Kasten, Norbert Brüggemann, Max Borsche, Tatiana Foroud, Eduardo Tolosa, Alicia Garrido, Grazia Annesi, Monica Gagliardi, Maria Bozi, Leonidas Stefanis, Joaquim José Ferreira, Leonor Correia Guedes, Micol Avenali, Simona Petrucci, Lorraine Clark, Ekaterina Y Fedotova, Natalya Y Abramycheva, Victoria Alvarez, Manuel Menéndez-González, Silvia Jesús Maestre, Pilar Gómez-Garre, Pablo Mir, Andrea Carmine Belin, Caroline Ran, Chin-Hsien Lin, Ming-Che Kuo, David Crosiers, Zbigniew K Wszolek, Owen A Ross, Joseph Jankovic, Kenya Nishioka, Manabu Funayama, Jordi Clarimon, Caroline H Williams-Gray, Marta Camacho, Mario R Cornejo-Olivas, Luis Torres-Ramirez, Yih-Ru Wu, Guey-Jen Lee-Chen, Ana Morgadinho, Teeratorn Pulkes, Pichet Termsarasab, Daniela Berg, Gregor Kuhlenbäumer, Andrea A Kühn, Friederike Borngräber, Giuseppe de Michele, Anna De Rosa, Alexander Zimprich, Andreas Puschmann, George D Mellick, Jolanta Dorszewska, Jonathan Carr, Rosangela Ferese, Stefano Gambardella, Bruce A Chase, Katerina Markopoulou, Wataru Satake, Tatsushi Toda, Malco Rossi, Marcelo Merello, Timothy Lynch, Diana Angelika Olszewska, Shen-Yang Lim, Azlina Ahmad-Annuar, Ai-Huey Tan, Bashayer Al-Mubarak, Hasmet Hanagasi, Dariusz Koziorowski, Sibel Ertan, Gençer Genç, Patricia de Carvalho Aguiar, Melinda Barkhuizen, Marcia M G Pimentel, Rachel Saunders-Pullman, Bart van de Warrenburg, Susan Bressman, Mathias Toft, Silke Appel-Cresswell, Anthony E Lang, Matej Skorvanek, Agnita J W Boon, Rejko Krüger, Esther M Sammler, Vitor Tumas, Bao-Rong Zhang, Gaetan Garraux, Sun Ju Chung, Yun Joong Kim, Juliane Winkelmann, Carolyn M Sue, Eng-King Tan, Joana Damásio, Péter Klivényi, Vladimir S Kostic, David Arkadir, Mika Martikainen, Vanderci Borges, Jens Michael Hertz, Laura Brighina, Mariana Spitz, Oksana Suchowersky, Olaf Riess, Parimal Das, Brit Mollenhauer, Emilia M Gatto, Maria Skaalum Petersen, Nobutaka Hattori, Ruey-Meei Wu, Sergey N Illarioshkin, Enza Maria Valente, Jan O Aasly, Anna Aasly, Roy N Alcalay, Avner Thaler, Matthew J Farrer, Kathrin Brockmann, Jean-Christophe Corvol, Christine Klein, null null
Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort. Movement disorders : official journal of the Movement Disorder Society 38 (2) (2023)
Eva-Juliane Vollstedt, Susen Schaake, Katja Lohmann, Shalini Padmanabhan, Alexis Brice, Suzanne Lesage, Christelle Tesson, Marie Vidailhet, Isabel Wurster, Faycel Hentati, Anat Mirelman, Nir Giladi, Karen Marder, Cheryl Waters, Stanley Fahn, Meike Kasten, Norbert Brüggemann, Max Borsche, Tatiana Foroud, Eduardo Tolosa, Alicia Garrido, Grazia Annesi, Monica Gagliardi, Maria Bozi, Leonidas Stefanis, Joaquim José Ferreira, Leonor Correia Guedes, Micol Avenali, Simona Petrucci, Lorraine Clark, Ekaterina Y Fedotova, Natalya Y Abramycheva, Victoria Alvarez, Manuel Menéndez-González, Silvia Jesús Maestre, Pilar Gómez-Garre, Pablo Mir, Andrea Carmine Belin, Caroline Ran, Chin-Hsien Lin, Ming-Che Kuo, David Crosiers, Zbigniew K Wszolek, Owen A Ross, Joseph Jankovic, Kenya Nishioka, Manabu Funayama, Jordi Clarimon, Caroline H Williams-Gray, Marta Camacho, Mario R Cornejo-Olivas, Luis Torres-Ramirez, Yih-Ru Wu, Guey-Jen Lee-Chen, Ana Morgadinho, Teeratorn Pulkes, Pichet Termsarasab, Daniela Berg, Gregor Kuhlenbäumer, Andrea A Kühn, Friederike Borngräber, Giuseppe de Michele, Anna De Rosa, Alexander Zimprich, Andreas Puschmann, George D Mellick, Jolanta Dorszewska, Jonathan Carr, Rosangela Ferese, Stefano Gambardella, Bruce A Chase, Katerina Markopoulou, Wataru Satake, Tatsushi Toda, Malco Rossi, Marcelo Merello, Timothy Lynch, Diana Angelika Olszewska, Shen-Yang Lim, Azlina Ahmad-Annuar, Ai-Huey Tan, Bashayer Al-Mubarak, Hasmet Hanagasi, Dariusz Koziorowski, Sibel Ertan, Gençer Genç, Patricia de Carvalho Aguiar, Melinda Barkhuizen, Marcia M G Pimentel, Rachel Saunders-Pullman, Bart van de Warrenburg, Susan Bressman, Mathias Toft, Silke Appel-Cresswell, Anthony E Lang, Matej Skorvanek, Agnita J W Boon, Rejko Krüger, Esther M Sammler, Vitor Tumas, Bao-Rong Zhang, Gaetan Garraux, Sun Ju Chung, Yun Joong Kim, Juliane Winkelmann, Carolyn M Sue, Eng-King Tan, Joana Damásio, Péter Klivényi, Vladimir S Kostic, David Arkadir, Mika Martikainen, Vanderci Borges, Jens Michael Hertz, Laura Brighina, Mariana Spitz, Oksana Suchowersky, Olaf Riess, Parimal Das, Brit Mollenhauer, Emilia M Gatto, Maria Skaalum Petersen, Nobutaka Hattori, Ruey-Meei Wu, Sergey N Illarioshkin, Enza Maria Valente, Jan O Aasly, Anna Aasly, Roy N Alcalay, Avner Thaler, Matthew J Farrer, Kathrin Brockmann, Jean-Christophe Corvol, Christine Klein, null null
Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort. Movement disorders : official journal of the Movement Disorder Society 38 (2) (2023)
Jon-Anders Tunold, Manuela M X Tan, Mathias Toft, Owen A Ross, Wilma D J van de Berg, Lasse Pihlstrom
Lysosomal Polygenic Burden Drives Cognitive Decline in Parkinson's Disease with Low Alzheimer Risk. Movement disorders : official journal of the Movement Disorder Society 39 (3) (2023)
Jon-Anders Tunold, Manuela M X Tan, Mathias Toft, Owen A Ross, Wilma D J van de Berg, Lasse Pihlstrom
Lysosomal Polygenic Burden Drives Cognitive Decline in Parkinson's Disease with Low Alzheimer Risk. Movement disorders : official journal of the Movement Disorder Society 39 (3) (2023)
Eva-Juliane Vollstedt, Susen Schaake, Katja Lohmann, Shalini Padmanabhan, Alexis Brice, Suzanne Lesage, Christelle Tesson, Marie Vidailhet, Isabel Wurster, Faycel Hentati, Anat Mirelman, Nir Giladi, Karen Marder, Cheryl Waters, Stanley Fahn, Meike Kasten, Norbert Brüggemann, Max Borsche, Tatiana Foroud, Eduardo Tolosa, Alicia Garrido, Grazia Annesi, Monica Gagliardi, Maria Bozi, Leonidas Stefanis, Joaquim José Ferreira, Leonor Correia Guedes, Micol Avenali, Simona Petrucci, Lorraine Clark, Ekaterina Y Fedotova, Natalya Y Abramycheva, Victoria Alvarez, Manuel Menéndez-González, Silvia Jesús Maestre, Pilar Gómez-Garre, Pablo Mir, Andrea Carmine Belin, Caroline Ran, Chin-Hsien Lin, Ming-Che Kuo, David Crosiers, Zbigniew K Wszolek, Owen A Ross, Joseph Jankovic, Kenya Nishioka, Manabu Funayama, Jordi Clarimon, Caroline H Williams-Gray, Marta Camacho, Mario R Cornejo-Olivas, Luis Torres-Ramirez, Yih-Ru Wu, Guey-Jen Lee-Chen, Ana Morgadinho, Teeratorn Pulkes, Pichet Termsarasab, Daniela Berg, Gregor Kuhlenbäumer, Andrea A Kühn, Friederike Borngräber, Giuseppe de Michele, Anna De Rosa, Alexander Zimprich, Andreas Puschmann, George D Mellick, Jolanta Dorszewska, Jonathan Carr, Rosangela Ferese, Stefano Gambardella, Bruce A Chase, Katerina Markopoulou, Wataru Satake, Tatsushi Toda, Malco Rossi, Marcelo Merello, Timothy Lynch, Diana Angelika Olszewska, Shen-Yang Lim, Azlina Ahmad-Annuar, Ai-Huey Tan, Bashayer Al-Mubarak, Hasmet Hanagasi, Dariusz Koziorowski, Sibel Ertan, Gençer Genç, Patricia de Carvalho Aguiar, Melinda Barkhuizen, Marcia M G Pimentel, Rachel Saunders-Pullman, Bart van de Warrenburg, Susan Bressman, Mathias Toft, Silke Appel-Cresswell, Anthony E Lang, Matej Skorvanek, Agnita J W Boon, Rejko Krüger, Esther M Sammler, Vitor Tumas, Bao-Rong Zhang, Gaetan Garraux, Sun Ju Chung, Yun Joong Kim, Juliane Winkelmann, Carolyn M Sue, Eng-King Tan, Joana Damásio, Péter Klivényi, Vladimir S Kostic, David Arkadir, Mika Martikainen, Vanderci Borges, Jens Michael Hertz, Laura Brighina, Mariana Spitz, Oksana Suchowersky, Olaf Riess, Parimal Das, Brit Mollenhauer, Emilia M Gatto, Maria Skaalum Petersen, Nobutaka Hattori, Ruey-Meei Wu, Sergey N Illarioshkin, Enza Maria Valente, Jan O Aasly, Anna Aasly, Roy N Alcalay, Avner Thaler, Matthew J Farrer, Kathrin Brockmann, Jean-Christophe Corvol, Christine Klein, null null
Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort. Movement disorders : official journal of the Movement Disorder Society 38 (2) (2023)
Hiroaki Sekiya, Shunsuke Koga, Aya Murakami, Michael DeTure, Owen A Ross, Ryan J Uitti, William P Cheshire, Zbigniew K Wszolek, Dennis W Dickson
Frequency of Comorbid Pathologies and Their Clinical Impact in Multiple System Atrophy. Movement disorders : official journal of the Movement Disorder Society (2023)
Jon-Anders Tunold, Manuela M X Tan, Mathias Toft, Owen A Ross, Wilma D J van de Berg, Lasse Pihlstrom
Lysosomal Polygenic Burden Drives Cognitive Decline in Parkinson's Disease with Low Alzheimer Risk. Movement disorders : official journal of the Movement Disorder Society (2023)
Eva-Juliane Vollstedt, Susen Schaake, Katja Lohmann, Shalini Padmanabhan, Alexis Brice, Suzanne Lesage, Christelle Tesson, Marie Vidailhet, Isabel Wurster, Faycel Hentati, Anat Mirelman, Nir Giladi, Karen Marder, Cheryl Waters, Stanley Fahn, Meike Kasten, Norbert Brüggemann, Max Borsche, Tatiana Foroud, Eduardo Tolosa, Alicia Garrido, Grazia Annesi, Monica Gagliardi, Maria Bozi, Leonidas Stefanis, Joaquim José Ferreira, Leonor Correia Guedes, Micol Avenali, Simona Petrucci, Lorraine Clark, Ekaterina Y Fedotova, Natalya Y Abramycheva, Victoria Alvarez, Manuel Menéndez-González, Silvia Jesús Maestre, Pilar Gómez-Garre, Pablo Mir, Andrea Carmine Belin, Caroline Ran, Chin-Hsien Lin, Ming-Che Kuo, David Crosiers, Zbigniew K Wszolek, Owen A Ross, Joseph Jankovic, Kenya Nishioka, Manabu Funayama, Jordi Clarimon, Caroline H Williams-Gray, Marta Camacho, Mario R Cornejo-Olivas, Luis Torres-Ramirez, Yih-Ru Wu, Guey-Jen Lee-Chen, Ana Morgadinho, Teeratorn Pulkes, Pichet Termsarasab, Daniela Berg, Gregor Kuhlenbäumer, Andrea A Kühn, Friederike Borngräber, Giuseppe de Michele, Anna De Rosa, Alexander Zimprich, Andreas Puschmann, George D Mellick, Jolanta Dorszewska, Jonathan Carr, Rosangela Ferese, Stefano Gambardella, Bruce A Chase, Katerina Markopoulou, Wataru Satake, Tatsushi Toda, Malco Rossi, Marcelo Merello, Timothy Lynch, Diana Angelika Olszewska, Shen-Yang Lim, Azlina Ahmad-Annuar, Ai-Huey Tan, Bashayer Al-Mubarak, Hasmet Hanagasi, Dariusz Koziorowski, Sibel Ertan, Gençer Genç, Patricia de Carvalho Aguiar, Melinda Barkhuizen, Marcia M G Pimentel, Rachel Saunders-Pullman, Bart van de Warrenburg, Susan Bressman, Mathias Toft, Silke Appel-Cresswell, Anthony E Lang, Matej Skorvanek, Agnita J W Boon, Rejko Krüger, Esther M Sammler, Vitor Tumas, Bao-Rong Zhang, Gaetan Garraux, Sun Ju Chung, Yun Joong Kim, Juliane Winkelmann, Carolyn M Sue, Eng-King Tan, Joana Damásio, Péter Klivényi, Vladimir S Kostic, David Arkadir, Mika Martikainen, Vanderci Borges, Jens Michael Hertz, Laura Brighina, Mariana Spitz, Oksana Suchowersky, Olaf Riess, Parimal Das, Brit Mollenhauer, Emilia M Gatto, Maria Skaalum Petersen, Nobutaka Hattori, Ruey-Meei Wu, Sergey N Illarioshkin, Enza Maria Valente, Jan O Aasly, Anna Aasly, Roy N Alcalay, Avner Thaler, Matthew J Farrer, Kathrin Brockmann, Jean-Christophe Corvol, Christine Klein, null null
Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort. Movement disorders : official journal of the Movement Disorder Society 38 (2) (2023)
Eva-Juliane Vollstedt, Susen Schaake, Katja Lohmann, Shalini Padmanabhan, Alexis Brice, Suzanne Lesage, Christelle Tesson, Marie Vidailhet, Isabel Wurster, Faycel Hentati, Anat Mirelman, Nir Giladi, Karen Marder, Cheryl Waters, Stanley Fahn, Meike Kasten, Norbert Brüggemann, Max Borsche, Tatiana Foroud, Eduardo Tolosa, Alicia Garrido, Grazia Annesi, Monica Gagliardi, Maria Bozi, Leonidas Stefanis, Joaquim José Ferreira, Leonor Correia Guedes, Micol Avenali, Simona Petrucci, Lorraine Clark, Ekaterina Y Fedotova, Natalya Y Abramycheva, Victoria Alvarez, Manuel Menéndez-González, Silvia Jesús Maestre, Pilar Gómez-Garre, Pablo Mir, Andrea Carmine Belin, Caroline Ran, Chin-Hsien Lin, Ming-Che Kuo, David Crosiers, Zbigniew K Wszolek, Owen A Ross, Joseph Jankovic, Kenya Nishioka, Manabu Funayama, Jordi Clarimon, Caroline H Williams-Gray, Marta Camacho, Mario R Cornejo-Olivas, Luis Torres-Ramirez, Yih-Ru Wu, Guey-Jen Lee-Chen, Ana Morgadinho, Teeratorn Pulkes, Pichet Termsarasab, Daniela Berg, Gregor Kuhlenbäumer, Andrea A Kühn, Friederike Borngräber, Giuseppe de Michele, Anna De Rosa, Alexander Zimprich, Andreas Puschmann, George D Mellick, Jolanta Dorszewska, Jonathan Carr, Rosangela Ferese, Stefano Gambardella, Bruce A Chase, Katerina Markopoulou, Wataru Satake, Tatsushi Toda, Malco Rossi, Marcelo Merello, Timothy Lynch, Diana Angelika Olszewska, Shen-Yang Lim, Azlina Ahmad-Annuar, Ai-Huey Tan, Bashayer Al-Mubarak, Hasmet Hanagasi, Dariusz Koziorowski, Sibel Ertan, Gençer Genç, Patricia de Carvalho Aguiar, Melinda Barkhuizen, Marcia M G Pimentel, Rachel Saunders-Pullman, Bart van de Warrenburg, Susan Bressman, Mathias Toft, Silke Appel-Cresswell, Anthony E Lang, Matej Skorvanek, Agnita J W Boon, Rejko Krüger, Esther M Sammler, Vitor Tumas, Bao-Rong Zhang, Gaetan Garraux, Sun Ju Chung, Yun Joong Kim, Juliane Winkelmann, Carolyn M Sue, Eng-King Tan, Joana Damásio, Péter Klivényi, Vladimir S Kostic, David Arkadir, Mika Martikainen, Vanderci Borges, Jens Michael Hertz, Laura Brighina, Mariana Spitz, Oksana Suchowersky, Olaf Riess, Parimal Das, Brit Mollenhauer, Emilia M Gatto, Maria Skaalum Petersen, Nobutaka Hattori, Ruey-Meei Wu, Sergey N Illarioshkin, Enza Maria Valente, Jan O Aasly, Anna Aasly, Roy N Alcalay, Avner Thaler, Matthew J Farrer, Kathrin Brockmann, Jean-Christophe Corvol, Christine Klein, null null
Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort. Movement disorders : official journal of the Movement Disorder Society 38 (2) (2023)
Axel D Meneses, Shunsuke Koga, Zonghua Li, Justin O'Leary, Fuyao Li, Kai Chen, Aya Murakami, Wenhui Qiao, Aishe Kurti, Michael G Heckman, Launia White, Manling Xie, Yixing Chen, NiCole A Finch, Melina J Lim, Marion Delenclos, Michael A DeTure, Cynthia Linares, Nicholas B Martin, Tadafumi C Ikezu, Marka M van Blitterswijk, Long-Jun Wu, Pamela J McLean, Rosa Rademakers, Owen A Ross, Gourisankar Ghosh, Guojun Bu, Na Zhao
APOE2 Exacerbates TDP-43 Related Toxicity in the Absence of Alzheimer Pathology. Annals of neurology (2022)
Rebecca R Valentino, Chloe Ramnarine, Michael G Heckman, Patrick W Johnson, Alexandra I Soto-Beasley, Ronald L Walton, Shunsuke Koga, Koji Kasanuki, Melissa E Murray, Ryan J Uitti, Julie A Fields, Hugo Botha, Vijay K Ramanan, Kejal Kantarci, Val J Lowe, Clifford R Jack, Nilufer Ertekin-Taner, Rodolfo Savica, Jonathan Graff-Radford, Ronald C Petersen, Joseph E Parisi, R Ross Reichard, Neill R Graff-Radford, Tanis J Ferman, Bradley F Boeve, Zbigniew K Wszolek, Dennis W Dickson, Owen A Ross
Mitochondrial genomic variation in dementia with Lewy bodies: association with disease risk and neuropathological measures. Acta neuropathologica communications 10 (1) (2022)
Franziska Hopfner, Anja K Tietz, Viktoria C Ruf, Owen A Ross, Shunsuke Koga, Dennis Dickson, Adriano Aguzzi, Johannes Attems, Thomas Beach, Allison Beller, William P Cheshire, Vivianna van Deerlin, Paula Desplats, Guenther Deuschl, Charles Duyckaerts, David Ellinghaus, Valentin Evsyukov, Margaret Ellen Flanagan, Andre Franke, Matthew P Frosch, Marla Gearing, Ellen Gelpí, Jay A van Gerpen, Bernardino Ghetti, Jonathan D Glass, Lea T Grinberg, Glenda M Halliday, Ingo Helbig, Matthias Höllerhage, Inge Huitinga, David John Irwin, Dirk C Keene, Gabor G Kovacs, Edward B Lee, Johannes Levin, Maria J Martí, Ian Mackenzie, Ian McKeith, Catriona Mclean, Brit Mollenhauer, Manuela Neumann, Kathy L Newell, Alexander Y Pantelyat, Manuela Pendziwiat, Annette Peters, Laura Molina Porcel, Alberto Rabano, Radoslav Matěj, Alex Rajput, Ali Rajput, Regina Reimann, William K Scott, William Seeley, Sashika Selvackadunco, Tanya Simuni, Christine Stadelmann, Per Svenningsson, Alan Thomas, Claudia Trenkwalder, Claire Troakes, John Q Trojanowski, Ryan J Uitti, Charles L White, Zbigniew K Wszolek, Tao Xie, Teresa Ximelis, Justo Yebenes, null null, Ulrich Müller, Gerard D Schellenberg, Jochen Herms, Gregor Kuhlenbäumer, Günter U Höglinger
Common Variants Near ZIC1 and ZIC4 in Autopsy-Confirmed Multiple System Atrophy. Movement disorders : official journal of the Movement Disorder Society 37 (10) (2022)
Axel D Meneses, Shunsuke Koga, Zonghua Li, Justin O'Leary, Fuyao Li, Kai Chen, Aya Murakami, Wenhui Qiao, Aishe Kurti, Michael G Heckman, Launia White, Manling Xie, Yixing Chen, Nicole A Finch, Melina J Lim, Marion Delenclos, Michael A DeTure, Cynthia Linares, Nicholas B Martin, Tadafumi C Ikezu, Marka M van Blitterswijk, Long-Jun Wu, Pamela J McLean, Rosa Rademakers, Owen A Ross, Gourisankar Ghosh, Guojun Bu, Na Zhao
APOE2 Exacerbates TDP-43 Related Toxicity in the Absence of Alzheimer Pathology. Annals of neurology (2022)
Paolo Reho, Shunsuke Koga, Zalak Shah, Ruth Chia, null null, null null, Rosa Rademakers, Clifton L Dalgard, Bradley F Boeve, Thomas G Beach, Dennis W Dickson, Owen A Ross, Sonja W Scholz
GRN Mutations Are Associated with Lewy Body Dementia. Movement disorders : official journal of the Movement Disorder Society 37 (9) (2022)
Lukasz M Milanowski, Olajumoke Oshinaike, Ronald L Walton, Alexandra I Soto-Beasley, Rana Hanna Al-Shaikh, Audrey J Strongosky, Owen A Ross, Zbigniew K Wszolek, Shamsideen Abayomi Ogun
Screening of GBA Mutations in Nigerian Patients with Parkinson's Disease. Movement disorders : official journal of the Movement Disorder Society (2021)
Chia-Chen Liu, Melissa E Murray, Xia Li, Na Zhao, Na Wang, Michael G Heckman, Francis Shue, Yuka A Martens, Yonghe Li, Ana-Caroline Raulin, Cassandra L Rosenberg, Sydney V Doss, Jing Zhao, Melissa C Wren, Lin Jia, Yingxue Ren, Tadafumi C Ikezu, Wenyan Lu, Yuan Fu, Thomas R Caulfield, Zachary A Trottier, Joshua Knight, Yixing Chen, Cynthia Linares, Xue Wang, Aishe Kurti, Yan W Asmann, Zbigniew K Wszolek, Glenn E Smith, Prashanthi Vemuri, Kejal Kantarci, David S Knopman, Val J Lowe, Clifford R Jack, Joseph E Parisi, Tanis J Ferman, Bradley F Boeve, Neill R Graff-Radford, Ronald C Petersen, Steven G Younkin, John D Fryer, Hu Wang, Xianlin Han, Carl Frieden, Gourisankar Ghosh, Owen A Ross, Guojun Bu
APOE3-Jacksonville (V236E) variant reduces self-aggregation and risk of dementia. Science translational medicine 13 (613) (2021)
Dongbing Lai, Babak Alipanahi, Pierre Fontanillas, Tae-Hwi Schwantes-An, Jan Aasly, Roy N Alcalay, Gary W Beecham, Daniela Berg, Susan Bressman, Alexis Brice, Kathrin Brockman, Lorraine Clark, Mark Cookson, Sayantan Das, Vivianna Van Deerlin, Jordan Follett, Matthew J Farrer, Joanne Trinh, Thomas Gasser, Stefano Goldwurm, Emil Gustavsson, Christine Klein, Anthony E Lang, J William Langston, Jeanne Latourelle, Timothy Lynch, Karen Marder, Connie Marras, Eden R Martin, Cory Y McLean, Helen Mejia-Santana, Eric Molho, Richard H Myers, Karen Nuytemans, Laurie Ozelius, Haydeh Payami, Deborah Raymond, Ekaterina Rogaeva, Michael P Rogers, Owen A Ross, Ali Samii, Rachel Saunders-Pullman, Birgitt Schüle, Claudia Schulte, William K Scott, Caroline Tanner, Eduardo Tolosa, James E Tomkins, Dolores Vilas, John Q Trojanowski, null null, Ryan Uitti, Jeffery M Vance, Naomi P Visanji, Zbigniew K Wszolek, Cyrus P Zabetian, Anat Mirelman, Nir Giladi, Avi Orr Urtreger, Paul Cannon, Brian Fiske, Tatiana Foroud
Genomewide Association Studies of LRRK2 Modifiers of Parkinson's Disease. Annals of neurology 90 (1) (2021)
Amica C Müller-Nedebock, Morenikeji A Komolafe, Michael B Fawale, Jonathan A Carr, Francois H van der Westhuizen, Owen A Ross, Soraya Bardien
Copy Number Variation in Parkinson's Disease: An Update from Sub-Saharan Africa. Movement disorders : official journal of the Movement Disorder Society 36 (10) (2021)
Angela M Crist, Kelly M Hinkle, Xue Wang, Christina M Moloney, Billie J Matchett, Sydney A Labuzan, Isabelle Frankenhauser, Nkem O Azu, Amanda M Liesinger, Elizabeth R Lesser, Daniel J Serie, Zachary S Quicksall, Tulsi A Patel, Troy P Carnwath, Michael DeTure, Xiaojia Tang, Ronald C Petersen, Ranjan Duara, Neill R Graff-Radford, Mariet Allen, Minerva M Carrasquillo, Hu Li, Owen A Ross, Nilüfer Ertekin-Taner, Gourisankar Ghosh, Yan W Asmann, Rickey E Carter, Melissa E Murray
Transcriptomic analysis to identify genes associated with selective hippocampal vulnerability in Alzheimer's disease. Nature communications 12 (1) (2021)
Keith Anthony Josephs, Joseph R Duffy, Heather M Clark, Rene L Utianski, Edythe A Strand, Mary M Machulda, Hugo Botha, Peter R Martin, Nha Trang Thu Pham, Julie Stierwalt, Farwa Ali, Marina Buciuc, Matthew Baker, Cristhoper H Fernandez De Castro, Anthony J Spychalla, Christopher G Schwarz, Robert I Reid, Matthew L Senjem, Clifford R Jack, Val J Lowe, Eileen H Bigio, Ross R Reichard, Eric J Polley, Nilufer Ertekin-Taner, Rosa Rademakers, Michael A DeTure, Owen A Ross, Gourisankar Ghosh, Jennifer L Whitwell
A molecular pathology, neurobiology, biochemical, genetic and neuroimaging study of progressive apraxia of speech. Nature communications 12 (1) (2021)
Tania F Gendron, Mohammed K Badi, Michael G Heckman, Karen R Jansen-West, George Koshy Vilanilam, Patrick W Johnson, Alexander R Burch, Ronald L Walton, Owen A Ross, Thomas G Brott, Timothy M Miller, James D Berry, Katharine A Nicholson, Zbigniew K Wszolek, Björn E Oskarsson, Kevin Navin Sheth, Lauren Hachmann Sansing, Guido J Falcone, Brett L Cucchiara, James F Meschia, Leonard Petrucelli
Plasma neurofilament light predicts mortality in patients with stroke. Science translational medicine 12 (569) (2021)
Rebecca R Valentino, Michael G Heckman, Patrick W Johnson, Matthew C Baker, Alexandra I Soto-Beasley, Ronald L Walton, Shunsuke Koga, Shanu F Roemer, EunRan Suh, Ryan J Uitti, John Q Trojanowski, Murray Grossman, Vivianna M Van Deerlin, Rosa Rademakers, Zbigniew K Wszolek, Gourisankar Ghosh, Owen A Ross
Association of Mitochondrial DNA Genomic Variation With Risk of Pick Disease. Neurology 96 (13) (2021)
Na Zhao, Olivia N Attrebi, Yingxue Ren, Wenhui Qiao, Berkiye Sonustun, Yuka A Martens, Axel D Meneses, Fuyao Li, Francis Shue, Jiaying Zheng, Alexandra J Van Ingelgom, Mary D Davis, Aishe Kurti, Joshua A Knight, Cynthia Linares, Yixing Chen, Pamela J McLean, Chia-Chen Liu, John D Fryer, Yan W Asmann, Pamela J McLean, Gourisankar Ghosh, Owen A Ross, Guojun Bu
APOE4 exacerbates α-synuclein pathology and related toxicity independent of amyloid. Science translational medicine 12 (529) (2021)
Ruth Chia, Marya S Sabir, Sara Bandres-Ciga, Sara Saez-Atienzar, Regina Hertfelder Reynolds, Emil Karl Gustavsson, Ronald L Walton, Sarah Ahmed, Coralie Viollet, Jinhui Ding, Mary B Makarious, Mónica Diez-Fairen, Makayla K Portley, Zalak Shah, Yevgeniya Abramzon, Dena G Hernandez, Cornelis Blauwendraat, David J Stone, John Eicher, Laura Parkkinen, Olaf Ansorge, Lorraine Clark, Lawrence S Honig, Karen Marder, Afina Lemstra, Peter St George-Hyslop, Elisabet Londos, Kevin Morgan, Tammaryn Lashley, Thomas T Warner, Zane Jaunmuktane, Douglas Galasko, Isabel Santana, Pentti J Tienari, Liisa Myllykangas, Minna Oinas, Nigel J Cairns, John C Morris, Glenda M Halliday, Vivanna M Van Deerlin, John Q Trojanowski, Maurizio Grassano, Andrea Calvo, Gabriele Mora, Antonio Canosa, Gianluca Floris, Ryan C Bohannan, Francesca Brett, Ziv Gan Or, Joshua T Geiger, Anni Moore, Patrick May, Rejko Krüger, David S Goldstein, Grisel Lopez, Nahid Tayebi, Ellen Sidransky, null null, Lucy Norcliffe-Kaufmann, Jose-Alberto Palma, Horacio Kaufmann, Vikram G Shakkottai, Matthew Perkins, Kathy L Newell, Thomas Gasser, Claudia Schulte, Francesco Landi, Erika Salvi, Daniele Cusi, Eliezer Masliah, Ronald C Kim, Chad A Caraway, Edwin S Monuki, Maura Brunetti, Ted M Dawson, Liana S Rosenthal, Marilyn S Albert, Olga Pletnikova, Juan C Troncoso, Margaret E Flanagan, Qinwen Mao, Eileen H Bigio, Eloy Rodríguez-Rodríguez, Jon Infante, Carmen Lage, Isabel González-Aramburu, Pascual Sánchez Juan, Bernardino Ghetti, Julia Keith, Sandra E Black, Mario Masellis, Ekaterina Rogaeva, Charles Duyckaerts, Alexis Brice, Suzanne Lesage, Georgia Xiromerisiou, Matthew J Barrett, Bension S Tilley, Steve Gentleman, Giancarlo Logroscino, Geidy E Serrano, Thomas G Beach, Ian G McKeith, Alan J Thomas, Johannes Attems, Christopher M Morris, Laura Palmer, Seth Love, Claire Troakes, Safa Al-Sarraj, Angela K Hodges, Dag Aarsland, Gregory Klein, Scott M Kaiser, Randy Woltjer, Pau Pastor, Lynn M Bekris, James B Leverenz, Lilah M Besser, Amanda Kuzma, Alan E Renton, Alison Mary Goate, David A Bennett, Clemens R Scherzer, Huw R Morris, Raffaele Ferrari, Diego Albani, Stuart Pickering-Brown, Kelley Faber, Walter A Kukull, Estrella Morenas-Rodriguez, Alberto Lleó, Juan Fortea, Daniel Alcolea, Jordi Clarimon, Mike A Nalls, Luigi Ferruci, Susan M Resnick, Toshiko Tanaka, Tatiana M Foroud, Neill R Graff-Radford, Zbigniew K Wszolek, Tanis Ferman, Bradley F Boeve, John A Hardy, Eric J Topol, Ali Torkamani, Andrew B Singleton, Mina Ryten, Dennis W Dickson, Adriano Chio, Owen A Ross, Raphael J Gibbs, Clifton L Dalgard, Bryan J Traynor, Sonja W Scholz
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture. Nature genetics 53 (3) (2021)
Anna I Wernick, Ronald L Walton, Alexandra I Soto-Beasley, Shunsuke Koga, Michael G Heckman, Rebecca R Valentino, Lukasz M Milanowski, Dorota Hoffman-Zacharska, Dariusz Koziorowski, Anhar Hassan, Ryan J Uitti, William P Cheshire, Wolfgang Singer, Zbigniew K Wszolek, Dennis W Dickson, Phillip A Low, Owen A Ross
Frequency of spinocerebellar ataxia mutations in patients with multiple system atrophy. Clinical autonomic research : official journal of the Clinical Autonomic Research Society 31 (1) (2021)
Lukasz M Milanowski, Owen A Ross, Andrzej Friedman, Dorota Hoffman-Zacharska, Paulina Gorka-Skoczylas, Marta Jurek, Dariusz Koziorowski, Zbigniew K Wszolek
Genetics of Parkinson's disease in the Polish population. Neurologia i neurochirurgia polska 55 (3) (2021)
Angela B Deutschlander, Takuya Konno, Alexandra I Soto-Beasley, Ronald L Walton, Jay A van Gerpen, Ryan J Uitti, Michael G Heckman, Zbigniew K Wszolek, Owen A Ross
Association of MAPT subhaplotypes with clinical and demographic features in Parkinson's disease. Annals of clinical and translational neurology 7 (9) (2020)
Rebecca R Valentino, Shunsuke Koga, Michael G Heckman, Danielle E Brushaber, Nancy N Diehl, Ronald L Walton, Gourisankar Ghosh, Owen A Ross
Association of Tripartite Motif Containing 11 rs564309 With Tau Pathology in Progressive Supranuclear Palsy. Movement disorders : official journal of the Movement Disorder Society 35 (5) (2020)
Rebecca R Valentino, Nikoleta Tamvaka, Michael G Heckman, Patrick W Johnson, Alexandra I Soto-Beasley, Ronald L Walton, Shunsuke Koga, Ryan J Uitti, Zbigniew K Wszolek, Dennis W Dickson, Owen A Ross
Associations of mitochondrial genomic variation with corticobasal degeneration, progressive supranuclear palsy, and neuropathological tau measures. Acta neuropathologica communications 8 (1) (2020)
Marina Buciuc, Jennifer L Whitwell, Koji Kasanuki, Jonathan Graff-Radford, Mary M Machulda, Joseph R Duffy, Edythe A Strand, Val J Lowe, Neill R Graff-Radford, Beth K Rush, Malgorzata B Franczak, Margaret E Flanagan, Matthew C Baker, Rosa Rademakers, Owen A Ross, Bernardino F Ghetti, Joseph E Parisi, Aditya Raghunathan, R Ross Reichard, Eileen H Bigio, Gourisankar Ghosh, Keith Anthony Josephs
Lewy Body Disease is a Contributor to Logopenic Progressive Aphasia Phenotype. Annals of neurology 89 (3) (2020)

Owen A Ross.css-eqlu8i{font-size:small;padding-left:4px;} (Owen Ross)

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Owen A Ross (Owen Ross)