Anna Morgan

ResearcherID Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 28

Top Venues

Genes

Biomedicines

European journal of human genetics : EJHG

Audiology research

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

Publications

Beatrice Spedicati, Aurora Santin, Giuseppe Giovanni Nardone, Elisa Rubinato, Stefania Lenarduzzi, Claudio Graziano, Livia Garavelli, Sara Miccoli, Stefania Bigoni, Anna Morgan, Giorgia Girotto
The Enigmatic Genetic Landscape of Hereditary Hearing Loss: A Multistep Diagnostic Strategy in the Italian Population. Biomedicines 11 (3) (2023)
Mariateresa Di Stazio, Caterina Zanus, Flavio Faletra, Alessia Pesaresi, Ilaria Ziccardi, Anna Morgan, Giorgia Girotto, Paola Costa, Marco Carrozzi, Adamo Pio D'Adamo, Luciana Musante
Haploinsufficiency as a Foreground Pathomechanism of Poirer-Bienvenu Syndrome and Novel Insights Underlying the Phenotypic Continuum of CSNK2B -Associated Disorders. Genes 14 (2) (2023)
Beatrice Spedicati, Aurora Santin, Giuseppe Giovanni Nardone, Elisa Rubinato, Stefania Lenarduzzi, Claudio Graziano, Livia Garavelli, Sara Miccoli, Stefania Bigoni, Anna Morgan, Giorgia Girotto
The Enigmatic Genetic Landscape of Hereditary Hearing Loss: A Multistep Diagnostic Strategy in the Italian Population. Biomedicines 11 (3) (2023)
Mariateresa Di Stazio, Caterina Zanus, Flavio Faletra, Alessia Pesaresi, Ilaria Ziccardi, Anna Morgan, Giorgia Girotto, Paola Costa, Marco Carrozzi, Adamo Pio D'Adamo, Luciana Musante
Haploinsufficiency as a Foreground Pathomechanism of Poirer-Bienvenu Syndrome and Novel Insights Underlying the Phenotypic Continuum of CSNK2B -Associated Disorders. Genes 14 (2) (2023)
Mariateresa Di Stazio, Caterina Zanus, Flavio Faletra, Alessia Pesaresi, Ilaria Ziccardi, Anna Morgan, Giorgia Girotto, Paola Costa, Marco Carrozzi, Adamo Pio D'Adamo, Luciana Musante
Haploinsufficiency as a Foreground Pathomechanism of Poirer-Bienvenu Syndrome and Novel Insights Underlying the Phenotypic Continuum of CSNK2B -Associated Disorders. Genes 14 (2) (2023)
Paola Tesolin, Aurora Santin, Anna Morgan, Stefania Lenarduzzi, Elisa Rubinato, Giorgia Girotto, Beatrice Spedicati
Which Came First? When Usher Syndrome Type 1 Couples with Neuropsychiatric Disorders. Audiology research 13 (6) (2023)
Paola Tesolin, Aurora Santin, Anna Morgan, Stefania Lenarduzzi, Elisa Rubinato, Giorgia Girotto, Beatrice Spedicati
Which Came First? When Usher Syndrome Type 1 Couples with Neuropsychiatric Disorders. Audiology research 13 (6) (2023)
Mariateresa Di Stazio, Caterina Zanus, Flavio Faletra, Alessia Pesaresi, Ilaria Ziccardi, Anna Morgan, Giorgia Girotto, Paola Costa, Marco Carrozzi, Adamo Pio D'Adamo, Luciana Musante
Haploinsufficiency as a Foreground Pathomechanism of Poirer-Bienvenu Syndrome and Novel Insights Underlying the Phenotypic Continuum of CSNK2B -Associated Disorders. Genes 14 (2) (2023)
Iain Mathieson, Felix R Day, Nicola Barban, Felix C Tropf, David M Brazel, null null, null null, Ahmad Vaez, Natalie van Zuydam, Bárbara D Bitarello, Eugene J Gardner, Evelina T Akimova, Ajuna Azad, Sven Bergmann, Lawrence F Bielak, Dorret I Boomsma, Kristina Bosak, Marco Brumat, Julie E Buring, David Cesarini, Daniel I Chasman, Jorge E Chavarro, Massimiliano Cocca, Maria Pina Concas, George Davey Smith, Gail Davies, Ian J Deary, Tõnu Esko, Jessica D Faul, null null, Oscar H Franco, Andrea Ganna, Audrey J Gaskins, Andrea Gelemanovic, Eco J C de Geus, Christian Gieger, Giorgia Girotto, Bamini Gopinath, Hans Jörgen Grabe, Erica P Gunderson, Caroline Hayward, Chunyan He, Diana van Heemst, W David Hill, Eva R Hoffman, Georg Homuth, Jouke- Jan Hottenga, Hongyang Huang, Elina Hyppӧnen, Mohammad Arfan Ikram, Rick Jansen, Magnus Johannesson, Zoha Kamali, Sharon L R Kardia, Maryam Kavousi, Annette Kifley, Tuomo Tapio Johannes Kiiskinen, Peter Kraft, Brigitte Kühnel, Claudia Langenberg, Gerald Liew, null null, Penelope A Lind, Jian'an Luan, Reedik Mägi, Patrik K E Magnusson, Anubha Mahajan, Nicholas G Martin, Hamdi Mbarek, Mark I McCarthy, George McMahon, Sarah E Medland, Thomas Meitinger, Andres Metspalu, Evelin Mihailov, Lili A Milani, Stacey A Missmer, Paul Mitchell, Stine Møllegaard, Dennis O Mook-Kanamori, Anna Morgan, Peter J van der Most, Renée de Mutsert, Matthias Nauck, Ilja Maria Nolte, Raymond Noordam, Brenda W J H Penninx, Annette Peters, Patricia A Peyser, Ozren Polašek, Chris Power, Ajka Pribisalic, Paul Redmond, Janet W Rich-Edwards, Paul M Ridker, Cornelius A Rietveld, Susan M Ring, Lynda M Rose, Rico Rueedi, Vallari Shukla, Jennifer A Smith, Stasa Stankovic, Kári Stefánsson, Doris Stöckl, Konstantin Strauch, Morris A Swertz, Alexander Teumer, Gudmar Thorleifsson, Unnur Thorsteinsdottir, A Roy Thurik, Nicholas John Timpson, Constance Turman, Andre G Uitterlinden, Melanie Waldenberger, Nicholas J Wareham, David R Weir, Gonneke Willemsen, Jing Hau Zhao, Wei Zhao, Yajie Zhao, Harold Snieder, Marcel den Hoed, Ken K Ong, Melinda C Mills, John R B Perry
Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus. Nature human behaviour (2023)
Aurora Santin, Beatrice Spedicati, Anna Morgan, Stefania Lenarduzzi, Paola Tesolin, Giuseppe Giovanni Nardone, Daniela Mazzà, Giovanni Di Lorenzo, Federica Romano, Francesca Buonomo, Alessandro Mangogna, Maria Pina Concas, Gabriella Zito, Giuseppe Ricci, Giorgia Girotto
Puzzling Out the Genetic Architecture of Endometriosis: Whole-Exome Sequencing and Novel Candidate Gene Identification in a Deeply Clinically Characterised Cohort. Biomedicines 11 (8) (2023)
Paola Tesolin, Aurora Santin, Anna Morgan, Stefania Lenarduzzi, Elisa Rubinato, Giorgia Girotto, Beatrice Spedicati
Which Came First? When Usher Syndrome Type 1 Couples with Neuropsychiatric Disorders. Audiology research 13 (6) (2023)
Iain Mathieson, Felix R Day, Nicola Barban, Felix C Tropf, David M Brazel, null null, null null, Ahmad Vaez, Natalie van Zuydam, Bárbara D Bitarello, Eugene J Gardner, Evelina T Akimova, Ajuna Azad, Sven Bergmann, Lawrence F Bielak, Dorret I Boomsma, Kristina Bosak, Marco Brumat, Julie E Buring, David Cesarini, Daniel I Chasman, Jorge E Chavarro, Massimiliano Cocca, Maria Pina Concas, George Davey Smith, Gail Davies, Ian J Deary, Tõnu Esko, Jessica D Faul, null null, Oscar H Franco, Andrea Ganna, Audrey J Gaskins, Andrea Gelemanovic, Eco J C de Geus, Christian Gieger, Giorgia Girotto, Bamini Gopinath, Hans Jörgen Grabe, Erica P Gunderson, Caroline Hayward, Chunyan He, Diana van Heemst, W David Hill, Eva R Hoffman, Georg Homuth, Jouke- Jan Hottenga, Hongyang Huang, Elina Hyppӧnen, Mohammad Arfan Ikram, Rick Jansen, Magnus Johannesson, Zoha Kamali, Sharon L R Kardia, Maryam Kavousi, Annette Kifley, Tuomo Tapio Johannes Kiiskinen, Peter Kraft, Brigitte Kühnel, Claudia Langenberg, Gerald Liew, null null, Penelope A Lind, Jian'an Luan, Reedik Mägi, Patrik K E Magnusson, Anubha Mahajan, Nicholas G Martin, Hamdi Mbarek, Mark I McCarthy, George McMahon, Sarah E Medland, Thomas Meitinger, Andres Metspalu, Evelin Mihailov, Lili A Milani, Stacey A Missmer, Paul Mitchell, Stine Møllegaard, Dennis O Mook-Kanamori, Anna Morgan, Peter J van der Most, Renée de Mutsert, Matthias Nauck, Ilja Maria Nolte, Raymond Noordam, Brenda W J H Penninx, Annette Peters, Patricia A Peyser, Ozren Polašek, Chris Power, Ajka Pribisalic, Paul Redmond, Janet W Rich-Edwards, Paul M Ridker, Cornelius A Rietveld, Susan M Ring, Lynda M Rose, Rico Rueedi, Vallari Shukla, Jennifer A Smith, Stasa Stankovic, Kári Stefánsson, Doris Stöckl, Konstantin Strauch, Morris A Swertz, Alexander Teumer, Gudmar Thorleifsson, Unnur Thorsteinsdottir, A Roy Thurik, Nicholas John Timpson, Constance Turman, Andre G Uitterlinden, Melanie Waldenberger, Nicholas J Wareham, David R Weir, Gonneke Willemsen, Jing Hau Zhao, Wei Zhao, Yajie Zhao, Harold Snieder, Marcel den Hoed, Ken K Ong, Melinda C Mills, John R B Perry
Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus. Nature human behaviour (2023)
Maria Pina Concas, Anna Morgan, Paola Tesolin, Aurora Santin, Giorgia Girotto, Paolo Gasparini
Sensory Capacities and Eating Behavior: Intriguing Results from a Large Cohort of Italian Individuals. Foods (Basel, Switzerland) 11 (5) (2022)
Paola Tesolin, Francesca Eleonora Bertinetto, Arianna Sonaglia, Stefania Cappellani, Maria Pina Concas, Anna Morgan, Norma Maria Ferrero, Alen Zabotti, Paolo Gasparini, Antonio Amoroso, Luca Quartuccio, Giorgia Girotto
High Throughput Genetic Characterisation of Caucasian Patients Affected by Multi-Drug Resistant Rheumatoid or Psoriatic Arthritis. Journal of personalized medicine 12 (10) (2022)
Beatrice Spedicati, Anna Morgan, Giulia Pianigiani, Luciana Musante, Elisa Rubinato, Aurora Santin, Giuseppe Giovanni Nardone, Flavio Faletra, Giorgia Girotto
Challenging Occam's Razor: Dual Molecular Diagnoses Explain Entangled Clinical Pictures. Genes 13 (11) (2022)
Beatrice Spedicati, Massimiliano Cocca, Roberto Palmisano, Flavio Faletra, Caterina Barbieri, Margherita Francescatto, Massimo Mezzavilla, Anna Morgan, Giulia Pelliccione, Paolo Gasparini, Giorgia Girotto
Natural human knockouts and Mendelian disorders: deep phenotyping in Italian isolates. European journal of human genetics : EJHG 29 (8) (2021)
Maria Pina Concas, Anna Morgan, Fabrizio Serra, Andries Paul Nagtegaal, Berthe C Oosterloo, Sudha Seshadri, Nancy Heard- Costa, Guy Van Camp, Erik Fransen, Margherita Francescatto, Giancarlo Logroscino, Rodolfo Sardone, Nicola Quaranta, Paolo Gasparini, Giorgia Girotto
Hearing Function: Identification of New Candidate Genes Further Explaining the Complexity of This Sensory Ability. Genes 12 (8) (2021)
Paola Tesolin, Sofia Fiorino, Stefania Lenarduzzi, Elisa Rubinato, Elisabetta Cattaruzzi, Lydie Ammar, Veronica Castro, Eva Orzan, Claudio Granata, Daniele Dell'Orco, Anna Morgan, Giorgia Girotto
Pendred Syndrome, or Not Pendred Syndrome? That Is the Question. Genes 12 (10) (2021)
Anna Morgan, Flavio Faletra, Giulia Severi, Martina La Bianca, Laura Licchetta, Paolo Gasparini, Claudio Graziano, Giorgia Girotto
There Is More Than Meets the Eye: Identification of Dual Molecular Diagnosis in Patients Affected by Hearing Loss. Biomedicines 10 (1) (2021)
Paola Tesolin, Anna Morgan, Michela Notarangelo, Rocco Pio Ortore, Maria Pina Concas, Angelantonio Notarangelo, Giorgia Girotto
Non-Syndromic Autosomal Dominant Hearing Loss: The First Italian Family Carrying a Mutation in the NCOA3 Gene. Genes 12 (7) (2021)
Maria Pina Concas, Alessandra Minelli, Susanna Aere, Anna Morgan, Paola Tesolin, Paolo Gasparini, Massimo Gennarelli, Giorgia Girotto
Genetic Dissection of Temperament Personality Traits in Italian Isolates. Genes 13 (1) (2021)
Anna Morgan, Savina Dipresa, Licia Turolla, Martina La Bianca, Flavio Faletra, Giorgia Girotto
A new case of TAR syndrome confirms the importance of noncoding variants in the etiopathogenesis of the disease. Human mutation 42 (2) (2020)
Anne E Justice, Tugce Karaderi, Heather M Highland, Kristin L Young, Mariaelisa Graff, Yingchang Lu, Valérie Turcot, Paul L Auer, Rebecca S Fine, Xiuqing Guo, Claudia Schurmann, Adelheid Lempradl, Eirini Marouli, Anubha Mahajan, Thomas W Winkler, Adam E Locke, Carolina Medina-Gomez, Tõnu Esko, Sailaja Vedantam, Ayush Giri, Ken Sin Lo, Tamuno Alfred, Poorva Mudgal, Maggie C Y Ng, Nancy Heard- Costa, Mary F Feitosa, Alisa K Manning, Sara M Willems, Suthesh Sivapalaratnam, Goncalo Abecasis, Dewan S Alam, Matthew Allison, Phillippe Amouyel, Zorayr Arzumanyan, Beverley Balkau, Lisa Bastarache, Sven Bergmann, Lawrence F Bielak, Matthias Blüher, Michael Boehnke, Heiner Boeing, Eric Boerwinkle, Carsten A Böger, Jette Bork-Jensen, Erwin P Bottinger, Donald W Bowden, Ivan Brandslund, Linda Broer, Amber A Burt, Adam S Butterworth, Mark J Caulfield, Giancarlo Cesana, John C Chambers, Daniel I Chasman, Yii-Der Ida Chen, Rajiv Chowdhury, Cramer Christensen, Audrey Y Chu, Francis S Collins, James P Cook, Amanda J Cox, David S Crosslin, John Danesh, Paul I W de Bakker, Simon de Denus, Renée de Mutsert, George Dedoussis, Ellen W Demerath, Joe G Dennis, Josh C Denny, Emanuele Di Angelantonio, Marcus Dörr, Fotios Drenos, Marie-Pierre Dubé, Alison M Dunning, Douglas F Easton, Paul Elliott, Evangelos Evangelou, Aliki-Eleni Farmaki, Shuang Feng, Ele Ferrannini, Jean Ferrieres, Jose C Florez, Myriam Fornage, Caroline S Fox, Paul W Franks, Nele Friedrich, Wei Gan, Ilaria Gandin, Paolo Gasparini, Vilmantas Giedraitis, Giorgia Girotto, Mathias Gorski, Harald Grallert, Niels Grarup, Megan L Grove, Stefan Gustafsson, Jeff Haessler, Torben Hansen, Andrew T Hattersley, Caroline Hayward, Iris M Heid, Oddgeir L Holmen, G Kees Hovingh, Joanna M M Howson, Yao Hu, Yi-Jen Hung, Kristian Hveem, Mohammad Arfan Ikram, Erik Ingelsson, Anne U Jackson, Gail P Jarvik, Yucheng Jia, Torben Jørgensen, Pekka Jousilahti, Johanne Marie Justesen, Bratati Kahali, Maria Karaleftheri, Sharon L R Kardia, Fredrik Karpe, Frank Kee, Hidetoshi Kitajima, Pirjo Komulainen, Jaspal S Kooner, Peter Kovacs, Bernhard K Krämer, Kari Kuulasmaa, Johanna Kuusisto, Markku Laakso, Timo A Lakka, David Lamparter, Leslie A Lange, Claudia Langenberg, Eric B Larson, Nanette R Lee, Wen-Jane Lee, Terho Lehtimäki, Cora E Lewis, Huaixing Li, Jin Li, Ruifang Li-Gao, Li-An Lin, Xu Lin, Lars Lind, Jaana Lindström, Allan Linneberg, Ching-Ti Liu, Dajiang J Liu, Jian'an Luan, Leo-Pekka Lyytikainen, Stuart Macgregor, Reedik Mägi, Satu Männistö, Gaëlle Marenne, Jonathan Marten, Nicholas G D Masca, Mark I McCarthy, Karina Meidtner, Evelin Mihailov, Leena Moilanen, Marie Moitry, Dennis O Mook-Kanamori, Anna Morgan, Andrew P Morris, Martina Müller-Nuraysid, Patricia B Munroe, Narisu Narisu, Christopher P Nelson, Matthew J Neville, Ioanna Ntalla, Jeffrey R O'Connell, Katharine R Owen, Oluf Pedersen, Gina M Peloso, Craig E Pennell, Markus Perola, James A Perry, John R B Perry, Tune H Pers, Ailith Ewing, Ozren Polasek, Olli T Raitakari, Asif Rasheed, Chelsea K Raulerson, Rainer Rauramaa, Dermot F Reilly, Alex P Reiner, Paul M Ridker, Manuel A Rivas, Neil R Robertson, Antonietta Robino, Igor Rudan, Katherine S Ruth, Danish Saleheen, Veikko V Salomaa, Nilesh J Samani, Pamela J Schreiner, Matthias B Schulze, Robert A Scott, Marcelo Segura-Lepe, Xueling S Sim, Andrew J Slater, Kerrin S Small, Blair Hamilton Smith, Jennifer A Smith, Lorraine Southam, Timothy D Spector, Elizabeth K Speliotes, Kári Stefánsson, Valgerdur Steinthorsdottir, Kathleen E Stirrups, Konstantin Strauch, Heather M Stringham, Michael Stumvoll, Liang Sun, Praveen Surendran, Karin M A Swart, Jean-Claude Tardif, Kent D Taylor, Alexander Teumer, Deborah J Thompson, Gudmar Thorleifsson, Unnur Thorsteinsdottir, Betina H Thuesen, Anke Tönjes, Mina Torres, Emmanouil Tsafantakis, Jaakko Tuomilehto, André G Uitterlinden, Matti Uusitupa, Cornelia M van Duijn, Mauno Vanhala, Rohit Varma, Sita H Vermeulen, Henrik Vestergaard, Veronique Vitart, Thomas F Vogt, Dragana Vuckovic, Lynne E Wagenknecht, Mark Walker, Lars Wallentin, Feijie Wang, Carol A Wang, Shuai Wang, Nicholas J Wareham, Helen R Warren, Dawn M Waterworth, Jennifer Wessel, Harvey D White, Cristen J Willer, James G Wilson, Andrew R Wood, Ying Wu, Hanieh Yaghootkar, Jie Yao, Laura M Yerges-Armstrong, Robin Young, Eleftheria Zeggini, Xiaowei Zhan, Weihua Zhang, Jing Hua Zhao, Wei Zhao, He Zheng, Wei Zhou, M Carola Zillikens, Fernando Rivadeneira, Ingrid B Borecki, John Andrew Pospisilik, Panagiotis Deloukas, Timothy M Frayling, Guillaume Lettre, Karen L Mohlke, Jerome I Rotter, Zoltán Kutalik, Joel N Hirschhorn, L Adrienne Cupples, Ruth J F Loos, Kari E North, Cecilia M Lindgren, null null, null null, null null, null null, null null, null null, null null, null null, null null, null null
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution. Nature genetics 51 (3) (2019)
Anna Morgan, Daniel C Koboldt, Elizabeth S Barrie, Erin R Crist, Gema García García, Massimo Mezzavilla, Flavio Faletra, Theresa Mihalic Mosher, Richard K Wilson, Catherine Blanchet, Kandamurugu Manickam, Anne-Francoise Roux, Paolo Gasparini, Daniele Dell'Orco, Giorgia Girotto
Mutations in PLS1, encoding fimbrin, cause autosomal dominant nonsyndromic hearing loss. Human mutation 40 (12) (2019)
Mariateresa Di Stazio, Chiara Collesi, Diego Vozzi, Wei Liu, Mike Myers, Anna Morgan, Pio Adamo D Adamo, Giorgia Girotto, Elisa Rubinato, Mauro Giacca, Paolo Gasparini
TBL1Y: a new gene involved in syndromic hearing loss. European journal of human genetics : EJHG 27 (3) (2018)
Anna Morgan, Dragana Vuckovic, Navaneethakrishnan Krishnamoorthy, Elisa Rubinato, Umberto Ambrosetti, Pierangela Castorina, Annamaria Franzè, Diego Vozzi, Martina La Bianca, Stefania Cappellani, Mariateresa Di Stazio, Paolo Gasparini, Giorgia Girotto
Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss. European journal of human genetics : EJHG 27 (1) (2018)
Evangelos Evangelou, Helen R Warren, David Mosen-Ansorena, Borbala Mifsud, Raha Pazoki, He Gao, Georgios Ntritsos, Niki Dimou, Claudia P Cabrera, Ibrahim Karaman, Fu Liang Ng, Marina Evangelou, Katarzyna Witkowska, Evan Tzanis, Jacklyn N Hellwege, Ayush Giri, Digna R Velez Edwards, Yan V Sun, Kelly Cho, J Michael Gaziano, Peter W F Wilson, Philip S Tsao, Csaba P Kovesdy, Tonu Esko, Reedik Mägi, Lili A Milani, Peter Almgren, Thibaud S Boutin, Stéphanie Debette, Jun Ding, Franco Giulianini, Elizabeth G Holliday, Anne U Jackson, Ruifang Li-Gao, Wei-Yu Lin, Jian'an Luan, Massimo Mangino, Christopher Oldmeadow, Bram Peter Prins, Yong Qian, Muralidharan Sargurupremraj, Nabi Shah, Praveen Surendran, Sébastien Thériault, Niek Verweij, Sara M Willems, Jing-Hua Zhao, Phillippe Amouyel, John Connell, Renée de Mutsert, Alex S F Doney, Martin Farrall, Cristina Menni, Andrew D Morris, Raymond Noordam, Guillaume Paré, Neil R Poulter, Denis C Shields, Alice V Stanton, Simon A M Thom, Gonçalo Abecasis, Najaf Amin, Dan E Arking, Kristin L Ayers, Caterina M Barbieri, Chiara Batini, Joshua C Bis, Tineka Blake, Murielle Bochud, Michael Boehnke, Eric Boerwinkle, Dorret I Boomsma, Erwin P Bottinger, Peter S Braund, Marco Brumat, Archie I Campbell, Harry Campbell, Aravinda Chakravarti, John C Chambers, Ganesh Chauhan, Marina Ciullo, Massimiliano Cocca, Francis S Collins, Heather J Cordell, Gail Davies, Martin H de Borst, Eco J C N de Geus, Ian J Deary, Joris Deelen, Fabiola Del Greco M, Cumhur Yusuf Demirkale, Marcus Dörr, Georg B Ehret, Roberto Elosua, Stefan Enroth, Abdullah Mesut Erzurumluoglu, Teresa Ferreira, Mattias Frånberg, Oscar H Franco, Ilaria Gandin, Paolo Gasparini, Vilmantas Giedraitis, Christian Gieger, Giorgia Girotto, Anuj Goel, Alan J Gow, Vilmundur Gudnason, Xiuqing Guo, Ulf Gyllensten, Anders Hamsten, Tamara B Harris, Sarah E Harris, Catharina A Hartman, Aki Samuli Havulinna, Andrew A Hicks, Edith Hofer, Albert Hofman, Jouke-Jan Hottenga, Jennifer E Huffman, Shih-Jen Hwang, Erik Ingelsson, Alan James, Rick Jansen, Marjo-Riitta Jarvelin, Roby Joehanes, Åsa Johansson, Andrew D Johnson, Peter K Joshi, Pekka Jousilahti, Johan Wouter Jukema, Antti Jula, Mika Kähönen, Sekar Kathiresan, Bernard D Keavney, Kay-Tee Khaw, Paul Knekt, Joanne Knight, Ivana Kolcic, Jaspal S Kooner, Seppo Koskinen, Kati Kristiansson, Zoltán Kutalik, Maris Laan, Marty Larson, Lenore J Launer, Benjamin Lehne, Terho Lehtimäki, David C M Liewald, Li Lin, Lars Lind, Cecilia M Lindgren, YongMei Liu, Ruth J F Loos, Lorna M Lopez, Yingchang Lu, Leo-Pekka Lyytikainen, Anubha Mahajan, Chrysovalanto Mamasoula, Jaume Marrugat, Jonathan Marten, Yuri Milaneschi, Anna Morgan, Andrew P Morris, Alanna C Morrison, Peter J Munson, Mike A Nalls, Priyanka Nandakumar, Christopher P Nelson, Teemu Niiranen, Ilja Maria Nolte, Teresa Nutile, Albertine J Oldehinkel, Ben A Oostra, Paul F O'Reilly, Elin Org, Sandosh Padmanabhan, Walter Palmas, Aarno Palotie, Alison Pattie, Brenda W J H Penninx, Markus Perola, Annette Peters, Ozren Polasek, Peter P Pramstaller, Quang Tri Nguyen, Olli T Raitakari, Meixia Ren, Rainer Rettig, Kenneth Rice, Paul M Ridker, Janina S Ried, Harriëtte Riese, Samuli Ripatti, Antonietta Robino, Lynda M Rose, Jerome I Rotter, Igor Rudan, Daniela Ruggiero, Yasaman Saba, Cinzia F Sala, Veikko V Salomaa, Nilesh J Samani, Antti-Pekka Sarin, Reinhold Schmidt, Helena Schmidt, Nick Shrine, David Siscovick, Albert Vernon Smith, Harold Snieder, Siim Sõber, Rossella Sorice, John M Starr, David J Stott, David P Strachan, Rona J Strawbridge, Johan Sundström, Morris A Swertz, Kent D Taylor, Alexander Teumer, Martin D Tobin, Maciej Tomaszewski, Daniela Toniolo, Michela Traglia, Stella Trompet, Jaakko Tuomilehto, Christophe Tzourio, André G Uitterlinden, Ahmad Vaez, Peter J van der Most, Cornelia M van Duijn, Anne-Claire Vergnaud, Germaine C Verwoert, Veronique Vitart, Uwe Völker, Peter Vollenweider, Dragana Vuckovic, Hugh Watkins, Sarah H Wild, Gonneke Willemsen, James F Wilson, Alan F Wright, Jie Yao, Tatijana Zemunik, Weihua Zhang, John Richard Attia, Adam S Butterworth, Daniel I Chasman, David Conen, Francesco Cucca, John Danesh, Caroline Hayward, Joanna M M Howson, Markku Laakso, Edward G Lakatta, Claudia Langenberg, Olle Melander, Dennis O Mook-Kanamori, Colin Neil Alexander Palmer, Lorenz Risch, Robert A Scott, Rodney J Scott, Peter Sever, Tim D Spector, Pim van der Harst, Nicholas J Wareham, Eleftheria Zeggini, Daniel Levy, Patricia B Munroe, Christopher Newton-Cheh, Morris J Brown, Andres Metspalu, Adriana M Hung, Christopher J O'Donnell, Todd L Edwards, Bruce M Psaty, Joanna Tzoulaki, Michael R Barnes, Louise V Wain, Paul Elliott, Mark J Caulfield, null null
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. Nature genetics 50 (10) (2018)
Dragana Vuckovic, Massimo Mezzavilla, Massimiliano Cocca, Anna Morgan, Marco Brumat, Eulalia Catamo, Maria Pina Concas, Ginevra Biino, Annamaria Franzè, Umberto Ambrosetti, Mario Pirastu, Paolo Gasparini, Giorgia Girotto
Whole-genome sequencing reveals new insights into age-related hearing loss: cumulative effects, pleiotropy and the role of selection. European journal of human genetics : EJHG 26 (8) (2018)

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Anna Morgan