Zbigniew K Wszolek (Z K Wszolek)

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 80

Top Topics

Amyotrophic Lateral Sclerosis

Genome Wide Association Study

Systematic Review

Hematopoietic Stem Cell

Top Venues

Nature genetics

Science translational medicine

Movement disorders : official journal of the Movement Disorder Society

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

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)
Dhairya A Lakhani, Xiangzhi Zhou, Shengzhen Tao, Vishal Patel, Sijin Wen, Lela Okromelidze, Elena Greco, Chen Lin, Erin M Westerhold, Sina Straub, Zbigniew K Wszolek, Philip Wade Tipton, Ryan J Uitti, Sanjeet S Grewal, Erik H Middlebrooks
Diagnostic utility of 7T neuromelanin imaging of the substantia nigra in Parkinson's disease. NPJ Parkinson's disease 10 (1) (2024)
Jarosław Dulski, Zbigniew K Wszolek
Heterogeneity of CSF1R-RD: Genes, Environment, or Both? Movement disorders : official journal of the Movement Disorder Society 39 (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 (2024)
Jordan D Marks, Virginia Estades Ayuso, Yari Carlomagno, Mei Yue, Tiffany W Todd, Ying Hao, Ziyi Li, Zachary T McEachin, Anantharaman Shantaraman, Duc M Duong, Lillian M Daughrity, Karen R Jansen-West, Wei Shao, Anna Calliari, Jesus Gonzalez Bejarano, Michael A DeTure, Bailey Rawlinson, Monica Castanedes Casey, Meredith T Lilley, Megan H Donahue, Vidhya Maheswari Jawahar, Bradley F Boeve, Ronald C Petersen, David S Knopman, Björn E Oskarsson, Neill R Graff-Radford, Zbigniew K Wszolek, Gourisankar Ghosh, Keith Anthony Josephs, Yue A Qi, Nicholas T Seyfried, Michael Emmerson Ward, Yong-Jie Zhang, Mercedes Prudencio, Leonard Petrucelli, Casey N Cook
TMEM106B core deposition associates with TDP-43 pathology and is increased in risk SNP carriers for frontotemporal dementia. Science translational medicine 16 (730) (2024)
Dhairya A Lakhani, Xiangzhi Zhou, Shengzhen Tao, Vishal Patel, Sijin Wen, Lela Okromelidze, Elena Greco, Chen Lin, Erin M Westerhold, Sina Straub, Zbigniew K Wszolek, Philip Wade Tipton, Ryan J Uitti, Sanjeet S Grewal, Erik H Middlebrooks
Diagnostic utility of 7T neuromelanin imaging of the substantia nigra in Parkinson's disease. NPJ Parkinson's disease 10 (1) (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)
Alexandra E Soto-Piña, Caroline C Pulido-Alvarado, Jarosław Dulski, Zbigniew K Wszolek, Jonathan Javier Magaña
Specific Biomarkers in Spinocerebellar Ataxia Type 3: A Systematic Review of Their Potential Uses in Disease Staging and Treatment Assessment. International journal of molecular sciences 25 (15) (2024)
Emily W Paolillo, Kaitlin B Casaletto, Annie L Clark, Jack Carson Taylor, Hilary W Heuer, Amy B Wise, Sreya Dhanam, Mark Sanderson-Cimino, Rowan Saloner, Joel H Kramer, John Kornak, Walter K Kremers, Leah K Forsberg, Brian S Appleby, Ece Bayram, Andrea Bozoki, Danielle Brushaber, Richard Ryan Darby, Gregory S Day, Bradford C Dickerson, Kimiko Domoto-Reilly, Fanny M Elahi, Julie A Fields, Nupur Ghoshal, Neill R Graff-Radford, Matthew G H Hall, Lawrence S Honig, Edward D Huey, Maria I Lapid, Irene Litvan, Ian R A Mackenzie, Joseph C Masdeu, Mario F Mendez, Carly T Mester, Toji Miyagawa, Georges Naasan, Maria B Pascual, Peter S Pressman, Eliana Marisa Ramos, Katherine P Rankin, Jessica E Rexach, Julio C Rojas, Lawren VandeVrede, Bonnie Wong, Zbigniew K Wszolek, Bradley F Boeve, Howard J Rosen, Adam L Boxer, Adam M Staffaroni, null null
Examining Associations Between Smartphone Use and Clinical Severity in Frontotemporal Dementia: Proof-of-Concept Study. JMIR aging 7 (2024)
Emily W Paolillo, Kaitlin B Casaletto, Annie L Clark, Jack Carson Taylor, Hilary W Heuer, Amy B Wise, Sreya Dhanam, Mark Sanderson-Cimino, Rowan Saloner, Joel H Kramer, John Kornak, Walter K Kremers, Leah K Forsberg, Brian S Appleby, Ece Bayram, Andrea Bozoki, Danielle Brushaber, Richard Ryan Darby, Gregory S Day, Bradford C Dickerson, Kimiko Domoto-Reilly, Fanny M Elahi, Julie A Fields, Nupur Ghoshal, Neill R Graff-Radford, Matthew G H Hall, Lawrence S Honig, Edward D Huey, Maria I Lapid, Irene Litvan, Ian R A Mackenzie, Joseph C Masdeu, Mario F Mendez, Carly T Mester, Toji Miyagawa, Georges Naasan, Maria B Pascual, Peter S Pressman, Eliana Marisa Ramos, Katherine P Rankin, Jessica E Rexach, Julio C Rojas, Lawren VandeVrede, Bonnie Wong, Zbigniew K Wszolek, Bradley F Boeve, Howard J Rosen, Adam L Boxer, Adam M Staffaroni, null null
Examining Associations Between Smartphone Use and Clinical Severity in Frontotemporal Dementia: Proof-of-Concept Study. JMIR aging 7 (2024)
Jarosław Dulski, Erik H Middlebrooks, Zbigniew K Wszolek
Novel Neuroimaging Pattern in POLR3A -Related Disorder on 7T MRI. Neurology. Genetics 10 (1) (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)
Jordan D Marks, Virginia Estades Ayuso, Yari Carlomagno, Mei Yue, Tiffany W Todd, Ying Hao, Ziyi Li, Zachary T McEachin, Anantharaman Shantaraman, Duc M Duong, Lillian M Daughrity, Karen R Jansen-West, Wei Shao, Anna Calliari, Jesus Gonzalez Bejarano, Michael A DeTure, Bailey Rawlinson, Monica Castanedes Casey, Meredith T Lilley, Megan H Donahue, Vidhya Maheswari Jawahar, Bradley F Boeve, Ronald C Petersen, David S Knopman, Björn E Oskarsson, Neill R Graff-Radford, Zbigniew K Wszolek, Gourisankar Ghosh, Keith Anthony Josephs, Yue A Qi, Nicholas T Seyfried, Michael Emmerson Ward, Yong-Jie Zhang, Mercedes Prudencio, Leonard Petrucelli, Casey N Cook
TMEM106B core deposition associates with TDP-43 pathology and is increased in risk SNP carriers for frontotemporal dementia. Science translational medicine 16 (730) (2024)
Jarosław Dulski, Erik H Middlebrooks, Zbigniew K Wszolek
Neuroimaging of CSF1R-related Disorder. Radiology 310 (1) (2024)
Jarosław Dulski, Matthew Baker, Samantha A Banks, Michael Bayat, Rose Bruffaerts, Gabriela Ortiz Cruz, Caio Cesar Diniz Disserol, Kristen S Fisher, Jainy N Jose, Bernadette Kalman, Orhun H Kantarci, Dmytro Maltsev, Catherine Middleton, Gabriela Novotni, Dijana Plaseska-Karanfilska, Salmo Raskin, Josiane Souza, Hélio Augusto Guizoni Teive, Zbigniew K Wszolek
Global Presence and Penetrance of CSF1R -Related Disorder. Neurology. Genetics 10 (5) (2024)
Jarosław Dulski, Erik H Middlebrooks, Zbigniew K Wszolek
Neuroimaging of CSF1R-related Disorder. Radiology 310 (1) (2024)
Jarosław Dulski, Erik H Middlebrooks, Zbigniew K Wszolek
Neuroimaging of CSF1R-related Disorder. Radiology 310 (1) (2024)
Jordan D Marks, Virginia Estades Ayuso, Yari Carlomagno, Mei Yue, Tiffany W Todd, Ying Hao, Ziyi Li, Zachary T McEachin, Anantharaman Shantaraman, Duc M Duong, Lillian M Daughrity, Karen R Jansen-West, Wei Shao, Anna Calliari, Jesus Gonzalez Bejarano, Michael A DeTure, Bailey Rawlinson, Monica Castanedes Casey, Meredith T Lilley, Megan H Donahue, Vidhya Maheswari Jawahar, Bradley F Boeve, Ronald C Petersen, David S Knopman, Björn E Oskarsson, Neill R Graff-Radford, Zbigniew K Wszolek, Gourisankar Ghosh, Keith Anthony Josephs, Yue A Qi, Nicholas T Seyfried, Michael Emmerson Ward, Yong-Jie Zhang, Mercedes Prudencio, Leonard Petrucelli, Casey N Cook
TMEM106B core deposition associates with TDP-43 pathology and is increased in risk SNP carriers for frontotemporal dementia. Science translational medicine 16 (730) (2024)
Jarosław Dulski, Zbigniew K Wszolek
Heterogeneity of CSF1R-RD: Genes, Environment, or Both? Movement disorders : official journal of the Movement Disorder Society 39 (7) (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)
Jarosław Dulski, Erik H Middlebrooks, Zbigniew K Wszolek
Neuroimaging of CSF1R-related Disorder. Radiology 310 (1) (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)
Jarosław Dulski, Peizhou Jiang, Wen-Lang Lin, Gourisankar Ghosh, Zbigniew K Wszolek
Assessment of Skin Biopsy as a Diagnostic Biomarker in CSF1R-Related Disorder. Neurology 102 (11) (2024)
Emily W Paolillo, Kaitlin B Casaletto, Annie L Clark, Jack Carson Taylor, Hilary W Heuer, Amy B Wise, Sreya Dhanam, Mark Sanderson-Cimino, Rowan Saloner, Joel H Kramer, John Kornak, Walter K Kremers, Leah K Forsberg, Brian S Appleby, Ece Bayram, Andrea Bozoki, Danielle Brushaber, Richard Ryan Darby, Gregory S Day, Bradford C Dickerson, Kimiko Domoto-Reilly, Fanny M Elahi, Julie A Fields, Nupur Ghoshal, Neill R Graff-Radford, Matthew G H Hall, Lawrence S Honig, Edward D Huey, Maria I Lapid, Irene Litvan, Ian R A Mackenzie, Joseph C Masdeu, Mario F Mendez, Carly T Mester, Toji Miyagawa, Georges Naasan, Maria B Pascual, Peter S Pressman, Eliana Marisa Ramos, Katherine P Rankin, Jessica E Rexach, Julio C Rojas, Lawren VandeVrede, Bonnie Wong, Zbigniew K Wszolek, Bradley F Boeve, Howard J Rosen, Adam L Boxer, Adam M Staffaroni, null null
Examining Associations Between Smartphone Use and Clinical Severity in Frontotemporal Dementia: Proof-of-Concept Study. JMIR aging 7 (2024)
Jordan D Marks, Virginia Estades Ayuso, Yari Carlomagno, Mei Yue, Tiffany W Todd, Ying Hao, Ziyi Li, Zachary T McEachin, Anantharaman Shantaraman, Duc M Duong, Lillian M Daughrity, Karen R Jansen-West, Wei Shao, Anna Calliari, Jesus Gonzalez Bejarano, Michael A DeTure, Bailey Rawlinson, Monica Castanedes Casey, Meredith T Lilley, Megan H Donahue, Vidhya Maheswari Jawahar, Bradley F Boeve, Ronald C Petersen, David S Knopman, Björn E Oskarsson, Neill R Graff-Radford, Zbigniew K Wszolek, Gourisankar Ghosh, Keith Anthony Josephs, Yue A Qi, Nicholas T Seyfried, Michael Emmerson Ward, Yong-Jie Zhang, Mercedes Prudencio, Leonard Petrucelli, Casey N Cook
TMEM106B core deposition associates with TDP-43 pathology and is increased in risk SNP carriers for frontotemporal dementia. Science translational medicine 16 (730) (2024)
Jarosław Dulski, Peizhou Jiang, Wen-Lang Lin, Gourisankar Ghosh, Zbigniew K Wszolek
Assessment of Skin Biopsy as a Diagnostic Biomarker in CSF1R-Related Disorder. Neurology 102 (11) (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)
Jordan D Marks, Virginia Estades Ayuso, Yari Carlomagno, Mei Yue, Tiffany W Todd, Ying Hao, Ziyi Li, Zachary T McEachin, Anantharaman Shantaraman, Duc M Duong, Lillian M Daughrity, Karen R Jansen-West, Wei Shao, Anna Calliari, Jesus Gonzalez Bejarano, Michael A DeTure, Bailey Rawlinson, Monica Castanedes Casey, Meredith T Lilley, Megan H Donahue, Vidhya Maheswari Jawahar, Bradley F Boeve, Ronald C Petersen, David S Knopman, Björn E Oskarsson, Neill R Graff-Radford, Zbigniew K Wszolek, Gourisankar Ghosh, Keith Anthony Josephs, Yue A Qi, Nicholas T Seyfried, Michael Emmerson Ward, Yong-Jie Zhang, Mercedes Prudencio, Leonard Petrucelli, Casey N Cook
TMEM106B core deposition associates with TDP-43 pathology and is increased in risk SNP carriers for frontotemporal dementia. Science translational medicine 16 (730) (2024)
Emily W Paolillo, Kaitlin B Casaletto, Annie L Clark, Jack Carson Taylor, Hilary W Heuer, Amy B Wise, Sreya Dhanam, Mark Sanderson-Cimino, Rowan Saloner, Joel H Kramer, John Kornak, Walter K Kremers, Leah K Forsberg, Brian S Appleby, Ece Bayram, Andrea Bozoki, Danielle Brushaber, Richard Ryan Darby, Gregory S Day, Bradford C Dickerson, Kimiko Domoto-Reilly, Fanny M Elahi, Julie A Fields, Nupur Ghoshal, Neill R Graff-Radford, Matthew G H Hall, Lawrence S Honig, Edward D Huey, Maria I Lapid, Irene Litvan, Ian R A Mackenzie, Joseph C Masdeu, Mario F Mendez, Carly T Mester, Toji Miyagawa, Georges Naasan, Maria B Pascual, Peter S Pressman, Eliana Marisa Ramos, Katherine P Rankin, Jessica E Rexach, Julio C Rojas, Lawren VandeVrede, Bonnie Wong, Zbigniew K Wszolek, Bradley F Boeve, Howard J Rosen, Adam L Boxer, Adam M Staffaroni, null null
Examining Associations Between Smartphone Use and Clinical Severity in Frontotemporal Dementia: Proof-of-Concept Study. JMIR aging 7 (2024)
Jarosław Dulski, Erik H Middlebrooks, Zbigniew K Wszolek
Novel Neuroimaging Pattern in POLR3A -Related Disorder on 7T MRI. Neurology. Genetics 10 (1) (2024)
Alexandra E Soto-Piña, Caroline C Pulido-Alvarado, Jarosław Dulski, Zbigniew K Wszolek, Jonathan Javier Magaña
Specific Biomarkers in Spinocerebellar Ataxia Type 3: A Systematic Review of Their Potential Uses in Disease Staging and Treatment Assessment. International journal of molecular sciences 25 (15) (2024)
Dhairya A Lakhani, Xiangzhi Zhou, Shengzhen Tao, Vishal Patel, Sijin Wen, Lela Okromelidze, Elena Greco, Chen Lin, Erin M Westerhold, Sina Straub, Zbigniew K Wszolek, Philip Wade Tipton, Ryan J Uitti, Sanjeet S Grewal, Erik H Middlebrooks
Diagnostic utility of 7T neuromelanin imaging of the substantia nigra in Parkinson's disease. NPJ Parkinson's disease 10 (1) (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)
Emily W Paolillo, Kaitlin B Casaletto, Annie L Clark, Jack Carson Taylor, Hilary W Heuer, Amy B Wise, Sreya Dhanam, Mark Sanderson-Cimino, Rowan Saloner, Joel H Kramer, John Kornak, Walter K Kremers, Leah K Forsberg, Brian S Appleby, Ece Bayram, Andrea Bozoki, Danielle Brushaber, Richard Ryan Darby, Gregory S Day, Bradford C Dickerson, Kimiko Domoto-Reilly, Fanny M Elahi, Julie A Fields, Nupur Ghoshal, Neill R Graff-Radford, Matthew G H Hall, Lawrence S Honig, Edward D Huey, Maria I Lapid, Irene Litvan, Ian R A Mackenzie, Joseph C Masdeu, Mario F Mendez, Carly T Mester, Toji Miyagawa, Georges Naasan, Maria B Pascual, Peter S Pressman, Eliana Marisa Ramos, Katherine P Rankin, Jessica E Rexach, Julio C Rojas, Lawren VandeVrede, Bonnie Wong, Zbigniew K Wszolek, Bradley F Boeve, Howard J Rosen, Adam L Boxer, Adam M Staffaroni, null null
Examining Associations Between Smartphone Use and Clinical Severity in Frontotemporal Dementia: Proof-of-Concept Study. JMIR aging 7 (2024)
Jordan D Marks, Virginia Estades Ayuso, Yari Carlomagno, Mei Yue, Tiffany W Todd, Ying Hao, Ziyi Li, Zachary T McEachin, Anantharaman Shantaraman, Duc M Duong, Lillian M Daughrity, Karen R Jansen-West, Wei Shao, Anna Calliari, Jesus Gonzalez Bejarano, Michael A DeTure, Bailey Rawlinson, Monica Castanedes Casey, Meredith T Lilley, Megan H Donahue, Vidhya Maheswari Jawahar, Bradley F Boeve, Ronald C Petersen, David S Knopman, Björn E Oskarsson, Neill R Graff-Radford, Zbigniew K Wszolek, Gourisankar Ghosh, Keith Anthony Josephs, Yue A Qi, Nicholas T Seyfried, Michael Emmerson Ward, Yong-Jie Zhang, Mercedes Prudencio, Leonard Petrucelli, Casey N Cook
TMEM106B core deposition associates with TDP-43 pathology and is increased in risk SNP carriers for frontotemporal dementia. Science translational medicine 16 (730) (2024)
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Validation Study of the MDS Criteria for the Diagnosis of Multiple System Atrophy in the Mayo Clinic Brain Bank. Neurology (2023)
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Potential use of glucocorticosteroids in CSF1R mutation carriers - current evidence and future directions. Neurologia i neurochirurgia polska (2023)
Hector Garcia-Moreno, Mercedes Prudencio, Gilbert Thomas-Black, Nita Solanky, Karen R Jansen-West, Rana Hanna Al-Shaikh, Amanda J Heslegrave, Henrik Zetterberg, Magda M Santana, Luis Pereira de Almeida, Ana Vasconcelos-Ferreira, Cristina Januário, Jon Infante, Jennifer Faber, Thomas Klockgether, Kathrin Reetz, Mafalda Raposo, Ana F Ferreira, Manuela Lima, Ludger Schöls, Matthis Synofzik, Jeannette Hübener, Andreas Puschmann, Sorina Gorcenco, Zbigniew K Wszolek, Leonard Petrucelli, Paola Giunti
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