Colm O’Dushlaine
Active 2005–2025
- Also published as
- Colm O'Dushlaine · Colm Ó'Dúshláine
- 51
- Papers
- 18,917
- Citations
- 40
- h-index
- 43
- i10-index
Citations
Citation sources
Countries
Institutions
Fields
- Biochemistry, Genetics and Molecular Biology47.1%
- Medicine35.6%
- Neuroscience10.2%
- Psychology3.4%
- Immunology and Microbiology1.1%
- Computer Science0.5%
- Other2.1%
Topics
- Genetic Associations and Epidemiology10.6%
- Genomics and Rare Diseases4.4%
- Genomic variations and chromosomal abnormalities3.5%
- Genetics and Neurodevelopmental Disorders3.4%
- Liver Disease Diagnosis and Treatment2.9%
- Lipid metabolism and disorders2.3%
- Other72.9%
Coauthors
- Joseph B. Leader9
- Anthony Marcketta8
- Aris Baras8
- Douglas M. Ruderfer8
- Evan K. Maxwell8
- Jennifer L. Moran8
- Joshua Backman8
- Shaun Purcell8
- Cristopher V. Van Hout7
- H. Lester Kirchner7
- John S. Penn7
- Kimberly Chambert7
- Lukas Habegger7
- Michael F. Murray7
- Pamela Sklar7
- Sarah E. Bergen7
- Stephan Ripke7
- Alexander Lopez6
- Frederick E. Dewey6
- Jeffrey G. Reid6
- John D. Overton6
- Patrick F. Sullivan6
- Shane McCarthy6
- Steven A. McCarroll6
All papers
- Biobank-driven genomic discovery yields new insight into atrial fibrillation biology
Authors: Jonas B. Nielsen, Rósa B. Þórólfsdóttir, Lars G. Fritsche, Wei Zhou, Morten W. Skov, Sarah E. Graham, Todd J. Herron, Shane McCarthy, Ellen M. Schmidt, Garðar Sveinbjörnsson, Ida Surakka, Michael R. Mathis, Masatoshi Yamazaki, Ryan Crawford, Maiken E. Gabrielsen, Anne Heidi Skogholt, Oddgeir L. Holmen, Maoxuan Lin, Brooke N. Wolford, Rounak Dey, Håvard Dalen, Patrick Sulem, Jonathan H. Chung, Joshua Backman, Davíð O. Arnar, Unnur Þorsteinsdóttir, Aris Baras, Colm O’Dushlaine, Anders G. Holst, Xiaoquan Wen, Whitney Hornsby, Frederick E. Dewey, Michael Boehnke, Sachin Kheterpal, Bhramar Mukherjee, Seunggeun Lee, Hyun Min Kang, Hilma Hólm, Jacob O. Kitzman, Jordan A. Shavit, José Jalife, Chad M. Brummett, Tanya M. Teslovich, David J. Carey, Daníel F. Guðbjartsson, Kāri Stefánsson, Gonçalo R. Abecasis, Kristian Hveem, Cristen J. Willer - Nature Genetics 2018 cited by 936
- A Protein-Truncating HSD17B13 Variant and Protection from Chronic Liver Disease
Authors: Noura S. Abul‐Husn, Xiping Cheng, Alexander Li, Yurong Xin, Claudia Schurmann, Panayiotis E. Stevis, Yashu Liu, Julia Kozlitina, Stefan Stender, G. Craig Wood, Ann Stepanchick, Matthew Still, Shane McCarthy, Colm O’Dushlaine, Jonathan S. Packer, Suganthi Balasubramanian, Nehal Gosalia, David Esopi, Sun Y. Kim, Semanti Mukherjee, Alexander Lopez, Erin D. Fuller, John S. Penn, Xin Chu, Jonathan Z. Luo, Uyenlinh L. Mirshahi, David J. Carey, Christopher D. Still, Michael D. Feldman, Aeron Small, Scott M. Damrauer, Daniel J. Rader, Brian Zambrowicz, William C. Olson, Andrew Murphy, Ingrid B. Borecki, Alan R. Shuldiner, Jeffrey G. Reid, John D. Overton, George D. Yancopoulos, Helen H. Hobbs, Jonathan C. Cohen, Omri Gottesman, Tanya M. Teslovich, Aris Baras, Tooraj Mirshahi, Jesper Gromada, Frederick E. Dewey - New England Journal of Medicine 2018 cited by 805
- Genetic and Pharmacologic Inactivation of ANGPTL3 and Cardiovascular Disease
Authors: Frederick E. Dewey, Viktoria Gusarova, Richard L. Dunbar, Colm O’Dushlaine, Claudia Schurmann, Omri Gottesman, Shane McCarthy, Cristopher V. Van Hout, Shannon Bruse, Hayes M. Dansky, Joseph B. Leader, Michael F. Murray, Marylyn D. Ritchie, H. Lester Kirchner, Lukas Habegger, Alex Lopez, John S. Penn, An Sha Zhao, Weiping Shao, Neil Stahl, Andrew Murphy, Sara Hamon, Aurelie Bouzelmat, Rick Zhang, Brad Shumel, Robert Pordy, Daniel A. Gipe, Gary Herman, Wayne Huey‐Herng Sheu, I‐Te Lee, Kae‐Woei Liang, Xiuqing Guo, Jerome I. Rotter, Yii‐Der I. Chen, William E. Kraus, Svati H. Shah, Scott M. Damrauer, Aeron Small, Daniel J. Rader, Anders Berg Wulff, Børge G. Nordestgaard, Anne Tybjærg‐Hansen, Anita M. van den Hoek, Hans M.G. Princen, David H. Ledbetter, David J. Carey, John D. Overton, Jeffrey G. Reid, William J. Sasiela, Poulabi Banerjee, Alan R. Shuldiner, Ingrid B. Borecki, Tanya M. Teslovich, George D. Yancopoulos, Scott Mellis, Jesper Gromada, Aris Baras - New England Journal of Medicine 2017 cited by 875
- Exome sequencing and characterization of 49,960 individuals in the UK Biobank
Authors: Cristopher V. Van Hout, Ioanna Tachmazidou, Joshua Backman, Joshua Hoffman, Daren Liu, Ashutosh Kumar Pandey, Claudia Gonzaga‐Jauregui, Shareef Khalid, Bin Ye, Nilanjana Banerjee, Alexander Li, Colm O’Dushlaine, Anthony Marcketta, Jeffrey Staples, Claudia Schurmann, Alicia Hawes, Evan K. Maxwell, Leland Barnard, Alexander Lopez, John S. Penn, Lukas Habegger, Andrew Blumenfeld, Xiaodong Bai, Sean O’Keeffe, Ashish Yadav, Kavita Praveen, Marcus B. Jones, William Salerno, Wendy K. Chung, Ida Surakka, Cristen J. Willer, Kristian Hveem, Joseph B. Leader, David J. Carey, David H. Ledbetter, Lon R. Cardon, George D. Yancopoulos, Aris N. Economides, Giovanni Coppola, Alan R. Shuldiner, Suganthi Balasubramanian, Michael Cantor, Matthew R. Nelson, John C. Whittaker, Jeffrey G. Reid, Jonathan Marchini, John D. Overton, Robert A. Scott, Gonçalo R. Abecasis, Laura M. Yerges-Armstrong, Aris Baras - Nature 2020 cited by 636
- Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
Authors: S Hong Lee, Sang Lee, Enda M Byrne, Enda M. Byrne, Naomi R. Wray, Stephan Ripke, Benjamin M Neale, Benjamin M. Neale, Stephan Ripke, Mark J. Daly, Verneri Anttila, Sarah E. Bergen, Sarah E Bergen, Lizzy Rossin, Benjamin M. Neale, Mark J. Daly, Stephan Ripke, Colm Ó'Dúshláine, Edward Scolnick, Edward M. Scolnick, Stephen V Faraone, Steven A. McCarroll, Jennifer L. Moran, Phil H Lee, Kimberly Chambert, Christine Fraser, Lyudmila Georgieva, Shaun Purcell, Douglas M. Ruderfer, Pamela Sklar, Peter A Holmans, Ian Jones, George K Kirov, Sarah E. Bergen, Ivan Nikolov, Michael J Owen, Peter Holmans, Stanley Zammit, Katherine Gordon‐Smith, Nicholas Craddock, Lyudmila Georgieva, John S Witte, Detelina Grozeva, Ian D. Jones, Marian L. Hamshere, Ole A Andreassen, Srdjan Djurovic, Morten Mattingsdal, Michael O‘Donovan, Michael J. Owen, Anita Thapar, Robert C Thompson, Stanley J Watson, Nicholas Craddock, Lyudmila Georgieva, Nicholas Bass, Ian D. Jones, Hugh Gurling, Radhika Kandaswamy, Michael O‘Donovan, Michael J. Owen, Anita Thapar, Michael E. Goddard, Michael E. Goddard, Richard Anney, Devin Absher, Richard M. Myers, Ingrid Agartz, Srdjan Djurovic, Morten Mattingsdal, Ole A. Andreassen, Ingrid Melle, Ingrid Agartz, Robert C. Thompson, Stanley J. Watson, Huda Akil, Fan Meng, Farooq Amin, Ole A. Andreassen, Ingrid Melle, Robert Krasucki, Adebayo Anjorin, Khalid Choudhury, Jacob Lawrence, Hugh Gurling, Jonathan Pimm, Nicholas Bass, Radhika Kandaswamy, Andrew McQuillin, Vinay Puri, Elaine Kenny, Aiden Corvin, Paul Cormican, Derek W. Morris, Richard Anney, Emma M. Quinn, Gary Donohoe, Michael Gill, Louise Gallagher, Dan E. Arking and 270 more - Nature Genetics 2013 cited by 2,353
- Computationally efficient whole genome regression for quantitative and binary traits
Authors: Joelle Mbatchou, Leland Barnard, Joshua Backman, Anthony Marcketta, Jack A. Kosmicki, Andrey Ziyatdinov, Christian Benner, Colm O’Dushlaine, Mathew Barber, Boris Boutkov, Lukas Habegger, Manuel A. R. Ferreira, Aris Baras, Jeffrey G. Reid, Gonçalo R. Abecasis, Evan K. Maxwell, Jonathan Marchini - Nature Genetics 2020 cited by 1,551
- Inactivating Variants in ANGPTL4 and Risk of Coronary Artery Disease
Authors: Frederick E. Dewey, Viktoria Gusarova, Colm O’Dushlaine, Omri Gottesman, Jesus Trejos, Charleen Hunt, Cristopher V. Van Hout, Lukas Habegger, David G. Buckler, Ka-Man V. Lai, Joseph B. Leader, Michael F. Murray, Marylyn D. Ritchie, H. Lester Kirchner, David H. Ledbetter, John S. Penn, Alexander Lopez, Ingrid B. Borecki, John D. Overton, Jeffrey G. Reid, David J. Carey, Andrew Murphy, George D. Yancopoulos, Aris Baras, Jesper Gromada, Alan R. Shuldiner - New England Journal of Medicine 2016 cited by 510
- Genetic identification of familial hypercholesterolemia within a single U.S. health care system
Authors: Noura S. Abul‐Husn, Kandamurugu Manickam, Laney K. Jones, Eric A. Wright, Dustin N. Hartzel, Claudia Gonzaga‐Jauregui, Colm O’Dushlaine, Joseph B. Leader, H. Lester Kirchner, D’Andra M. Lindbuchler, Marci L Barr, Monica A. Giovanni, Marylyn D. Ritchie, John D. Overton, Jeffrey G. Reid, Raghu Metpally, Amr H. Wardeh, Ingrid B. Borecki, George D. Yancopoulos, Aris Baras, Alan R. Shuldiner, Omri Gottesman, David H. Ledbetter, David J. Carey, Frederick E. Dewey, Michael F. Murray - Science 2016 cited by 428
- Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways
Authors: Colm Ó'Dúshláine, Lizzy Rossin, Laramie Duncan, Verneri Anttila, Benjamin M Neale, Laramie E. Duncan, Mark J. Daly, Verneri Anttila, Soumya Raychaudhuri, Lizzy Rossin, Phil H Lee, Sarah E Bergen, Jordan W Smoller, Jordan W. Smoller, Steven A McCarroll, Jennifer L Moran, Kimberly Chambert, Jordan W. Smoller, Sarah E. Bergen, Philip Asherson, Steven A. McCarroll, Soumya Raychaudhuri, Mark J. Daly, Edward M. Scolnick, Jennifer L. Moran, Laramie E. Duncan, Gerome Breen, Neelroop Parikshak, Cathryn M. Lewis, Philip Asherson, David Collier, Bryan J Mowry, Peter McGuffin, Anne Farmer, Jonna Kuntsi, Ian W. Craig, Stephen Newhouse, Stephen Newhouse, Katherine Gordon-Smith, Detelina Grozeva, Douglas M. Ruderfer, George K Kirov, Valentina Moskvina, Daniëlle Posthuma, Michael J Owen, Nigel Williams, Enda M. Byrne, Sang Lee, Nicholas Craddock, Naomi R. Wray, Pamela Sklar, Michael E Goddard, John S Witte, Tatiana Foroud, Daniel L Koller, Devin Absher, Richard M Myers, Anita Thapar, Ole A Andreassen, Ian Jones, Nigel Williams, Detelina Grozeva, Huda Akil, Peter Holmans, Michael J. Owen, Stanley J Watson, Farooq Amin, Adebayo Anjorin, Nicholas Bass, Khalid Choudhury, Hugh Gurling, Anita Thapar, Ian Jones, Nigel Williams, Pamela Sklar, Michael J. Owen, Vinay Puri, Richard Anney, Paul Cormican, Aiden Corvin, Gary J Donohoe, Louise Gallagher, John S. Witte, Daniel L. Koller, Tatiana Foroud, Richard M. Myers, Devin Absher, Srdjan Djurovic, Morten Mattingsdal, Maria H Azevedo, Ingrid Agartz, Lena Backlund, Ingrid Agartz, Huda Akil, Stanley J. Watson, Fan Meng, Robert C. Thompson, Farooq Amin, Tobias Banaschewski, Jack D Barchas and 275 more - Nature Neuroscience 2015 cited by 798
- Genome-wide association analysis identifies 13 new risk loci for schizophrenia
Authors: Stephan Ripke, Colm Ó'Dúshláine, Kimberly Chambert, Jennifer L. Moran, Anna K. Kähler, Susanne Akterin, Sarah E. Bergen, Ann L. Collins, James J Crowley, Menachem Fromer, Yunjung Kim, Sang Lee, Patrik K. E. Magnusson, Nick Sanchez, Eli A. Stahl, Stephanie Williams, Naomi R. Wray, Kai Xia, Francesco Bettella, Anders D. Børglum, Brendan Bulik‐Sullivan, Paul Cormican, Nick Craddock, Christiaan de Leeuw, Naser Durmishi, Michael Gill, В. Е. Голимбет, Marian L. Hamshere, Peter Holmans, David M Hougaard, Kenneth S. Kendler, Kuang Lin, Derek W. Morris, Ole Mors, Preben Bo Mortensen, Benjamin M. Neale, F. Anthony O’Neill, Michael J. Owen, Milica Pejovic Milovancevic, Daniëlle Posthuma, John Powell, Alexander Richards, Brien P. Riley, Douglas M. Ruderfer, Dan Rujescu, Engilbert Sigurðsson, Teimuraz Silagadze, August B. Smit, Hreinn Stefánsson, Stacy Steinberg, Jaana Suvisaari, Sarah Tosato, Matthijs Verhage, James Walters, Elvira Bramon, Aiden Corvin, Michael O‘Donovan, Kari Stefansson, Edward M. Scolnick, Shaun Purcell, Steven A. McCarroll, Pamela Sklar, Christina M. Hultman, Patrick F. Sullivan - Nature Genetics 2013 cited by 1,565
- Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study
Authors: Frederick E. Dewey, Michael F. Murray, John D. Overton, Lukas Habegger, Joseph B. Leader, Samantha N. Fetterolf, Colm O’Dushlaine, Cristopher V. Van Hout, Jeffrey Staples, Claudia Gonzaga‐Jauregui, Raghu Metpally, Sarah A. Pendergrass, Monica A. Giovanni, H. Lester Kirchner, Suganthi Balasubramanian, Noura S. Abul‐Husn, Dustin N. Hartzel, Daniel R. Lavage, Korey A. Kost, Jonathan S. Packer, Alexander Lopez, John S. Penn, Semanti Mukherjee, Nehal Gosalia, Manoj Kanagaraj, Alexander Li, Lyndon J. Mitnaul, Lance J. Adams, Thomas N. Person, Kavita Praveen, Anthony Marcketta, Matthew S. Lebo, Christina Austin‐Tse, Heather Mason‐Suares, Shannon Bruse, Scott Mellis, Robert S. Phillips, Neil Stahl, Andrew Murphy, Aris N. Economides, Kimberly A. Skelding, Christopher D. Still, James R. Elmore, Ingrid B. Borecki, George D. Yancopoulos, F. Daniel Davis, W. Andrew Faucett, Omri Gottesman, Marylyn D. Ritchie, Alan R. Shuldiner, Jeffrey G. Reid, David H. Ledbetter, Aris Baras, David J. Carey - Science 2016 cited by 607
- Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
Authors: Broad Genomics Platform, Jason Flannick, CHARGE, LuCamp, ProDiGY, GoT2D, ESP, SIGMA-T2D, T2D-GENES, AMP-T2D-GENES, Josep M. Mercader, Christian Fuchsberger, Miriam S. Udler, Anubha Mahajan, Jennifer Wessel, Tanya M. Teslovich, Lizz Caulkins, Ryan Koesterer, Francisco Barajas‐Olmos, Thomas W. Blackwell, Eric Boerwinkle, Jennifer A. Brody, Federico Centeno-Cruz, Chen Ling, Siying Chen, Cecilia Contreras-Cubas, Emilio J. Córdova, Adolfo Correa, Maria L. Cortés, Ralph A. DeFronzo, Lawrence M. Dolan, Kimberly L. Drews, Amanda Elliott, James S. Floyd, Stacey Gabriel, María Eugenia Garay-Sevilla, Humberto Garcia‐Ortíz, Myron Gross, Sohee Han, Nancy L. Heard‐Costa, Anne Jackson, Marit E. Jørgensen, Hyun Min Kang, Megan M. Kelsey, Bong-Jo Kim, Heikki A. Koistinen, Johanna Kuusisto, Joseph B. Leader, Allan Linneberg, Ching‐Ti Liu, Jianjun Liu, Valeriya Lyssenko, Alisa K. Manning, Anthony Marcketta, Juan Manuel Malacara-Hernández, Angélica Martínez‐Hernández, Karen Matsuo, Elizabeth J. Mayer‐Davis, Elvia Mendoza‐Caamal, Karen L. Mohlke, Alanna C. Morrison, Anne Ndungu, Maggie Ng, Colm O’Dushlaine, A. J. Payne, Catherine Pihoker, Wendy S. Post, Michael Preuß, Bruce M. Psaty, Ramachandran S. Vasan, N. William Rayner, Alexander P. Reiner, M. Revilla, Neil R. Robertson, Nicola Santoro, Claudia Schurmann, Wing Yee So, Xavier Soberón, Heather M. Stringham, Tim M. Strom, Claudia H. T. Tam, Farook Thameem, Brian Tomlinson, Jason Torres, Russell P. Tracy, Rob M. van Dam, Marijana Vujković, Shuai Wang, Ryan Welch, Daniel R. Witte, Tien Yin Wong, Gil Atzmon, Nir Barzilai, John Blangero, Lori L. Bonnycastle, Donald W. Bowden, John C. Chambers, Edmund Chan, Ching‐Yu Cheng, Yoon Shin Cho and 73 more - Nature 2019 cited by 338
- Association of Rare and Common Variation in the Lipoprotein Lipase Gene With Coronary Artery Disease
Authors: Amit V. Khera, Hong‐Hee Won, Gina M. Peloso, Colm O’Dushlaine, Dajiang J. Liu, Nathan O. Stitziel, Pradeep Natarajan, Akihiro Nomura, Connor A. Emdin, Namrata Gupta, Ingrid B. Borecki, Rosanna Asselta, Stefano Duga, Piera Angelica Merlini, Adolfo Correa, Thorsten Kessler, James G. Wilson, Matthew J. Bown, Alistair S. Hall, Peter S. Braund, David J. Carey, Michael F. Murray, H. Lester Kirchner, Joseph B. Leader, Daniel R. Lavage, J. Neil Manus, Dustin N. Hartzel, Nilesh J. Samani, Heribert Schunkert, Jaume Marrugat, Roberto Elosúa, Ruth McPherson, Martin Farrall, Hugh Watkins, Eric S. Lander, Daniel J. Rader, John Danesh, Diego Ardissino, Stacey Gabriel, Cristen J. Willer, Gonçalo R. Abecasis, Danish Saleheen, Frederick E. Dewey, Sekar Kathiresan - JAMA 2017 cited by 204
- A polygenic burden of rare disruptive mutations in schizophrenia
Authors: Shaun Purcell, Jennifer L. Moran, Menachem Fromer, Douglas M. Ruderfer, Nadia Solovieff, Panos Roussos, Colm Ó'Dúshláine, Kimberly Chambert, Sarah E. Bergen, Anna K. Kähler, Laramie E. Duncan, Eli Stahl, Giulio Genovese, Esperanza Fernández, Mark O. Collins, Noboru H. Komiyama, Jyoti S. Choudhary, Patrik K. E. Magnusson, Eric Banks, Khalid Shakir, Kiran Garimella, Tim Fennell, Mark A. DePristo, Seth G. N. Grant, Stephen J. Haggarty, Stacey Gabriel, Edward M. Scolnick, Eric S. Lander, Christina M. Hultman, Patrick F. Sullivan, Steven A. McCarroll, Pamela Sklar - Nature 2014 cited by 1,461
- Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease
Authors: Julie Horowitz, Jack A. Kosmicki, Amy Damask, Deepika Sharma, Genevieve H. L. Roberts, Anne E. Justice, Nilanjana Banerjee, Marie V. Coignet, Ashish Yadav, Joseph B. Leader, Anthony Marcketta, Danny S. Park, Rouel Lanche, Evan K. Maxwell, Spencer C. Knight, Xiaodong Bai, Harendra Guturu, Dylan Sun, Asher K. Haug Baltzell, Fabrício S. P. Kury, Joshua Backman, Ahna R. Girshick, Colm O’Dushlaine, Shannon McCurdy, Raghavendran Partha, Adam J. Mansfield, David A. Turissini, Alexander Li, Miao Zhang, Joelle Mbatchou, Kyoko Watanabe, Lauren Gurski, Shane McCarthy, Hyun Min Kang, Lee Dobbyn, Eli A. Stahl, Anurag Verma, Giorgio Sirugo, RGC Management and Leadership Team, Gonçalo R. Abecasis, Michael Cantor, Giovanni Coppola, Andrew Deubler, Aris N. Economides, Katia Karalis, Luca A. Lotta, Alan R. Shuldiner, Sequencing and Lab Operations, Christina Beechert, Caitlin Forsythe, Erin D. Fuller, Zhenhua Gu, Michael Lattari, Alexander Lopez, Maria Sotiropoulos Padilla, Manasi Pradhan, Kia Manoochehri, Thomas D. Schleicher, Louis Widom, Sarah E. Wolf, Ricardo H. Ulloa, Amelia Averitt, Dadong Li, Sameer Malhotra, Jeffrey Staples, Genome Informatics, Suying Bao, Boris Boutkov, Siying Chen, Gisu Eom, Alicia Hawes, Shareef Khalid, Olga Krasheninina, Rouel Lanche, Evan K. Maxwell, George Mitra, Mona Nafde, Sean O’Keeffe, Max Orelus, Razvan Panea, Tommy Polanco, Ayesha Rasool, Jeffrey G. Reid, William Salerno, Jeffrey Staples, Kathie Sun, Jiwen Xin, Analytical Genomics and Data Science, Joshua Backman, Manuel Allen Revez Ferreira, Arkopravo Ghosh, Christopher E. Gillies, Eric Jorgenson, Hyun Min Kang, Michael D. Kessler, Alexander Li, Nan Lin, Daren Liu, Adam E. Locke, Arden Moscati and 68 more - Nature Genetics 2022 cited by 179
- Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes
Authors: Viktoria Gusarova, Colm O’Dushlaine, Tanya M. Teslovich, Peter N. Benotti, Tooraj Mirshahi, Omri Gottesman, Cristopher V. Van Hout, Michael F. Murray, Anubha Mahajan, Jonas B. Nielsen, Lars G. Fritsche, Anders Berg Wulff, Daníel F. Guðbjartsson, Marketa Sjögren, Connor A. Emdin, Robert A. Scott, Wen‐Jane Lee, Aeron Small, Lydia Coulter Kwee, Om Prakash Dwivedi, Rashmi B. Prasad, Shannon Bruse, Alexander Lopez, John S. Penn, Anthony Marcketta, Joseph B. Leader, Christopher D. Still, H. Lester Kirchner, Uyenlinh L. Mirshahi, Amr H. Wardeh, Cassandra M. Hartle, Lukas Habegger, Samantha N. Fetterolf, Teresa Tusié‐Luna, Andrew P. Morris, Hilma Hólm, Valgerður Steinthórsdóttir, Patrick Sulem, Unnur Thorsteinsdottir, Jerome I. Rotter, Lee‐Ming Chuang, Scott M. Damrauer, David Birtwell, Chad M. Brummett, Amit V. Khera, Pradeep Natarajan, Marju Orho‐Melander, Jason Flannick, Luca A. Lotta, Cristen J. Willer, Oddgeir L. Holmen, Marylyn D. Ritchie, David H. Ledbetter, Andrew Murphy, Ingrid B. Borecki, Jeffrey G. Reid, John D. Overton, Ola Hansson, Leif Groop, Svati H. Shah, William E. Kraus, Daniel J. Rader, Yii‐Der Ida Chen, Kristian Hveem, Nicholas J. Wareham, Sekar Kathiresan, Olle Melander, Kāri Stefánsson, Børge G. Nordestgaard, Anne Tybjærg‐Hansen, Gonçalo R. Abecasis, David Altshuler, José C. Florez, Michael Boehnke, Mark I. McCarthy, George D. Yancopoulos, David J. Carey, Alan R. Shuldiner, Aris Baras, Frederick E. Dewey, Jesper Gromada - Nature Communications 2018 cited by 153
- Promoting the genomic revolution in Africa through the Nigerian 100K Genome Project
Authors: Segun Fatumo, Aminu Yakubu, Olubukunola Oyedele, Olajumoke Adeniji-Popoola, Delali Attiogbe Attipoe, Golibe Eze-Echesi, Fatima Z Modibbo, Nabila Ado-Wanka, 54gene Team, Yemisi Osakwe, Onome Braimah, Eramoh Julius-Enigimi, Terver Mark Akindigh, Bolutife Kusimo, Chinenye Akpulu, Chiamaka Nwuba, Ofonime Ebong, Chinyere Anyika, Oluwatimilehin Adewunmi, Yusuf Ibrahim, Janet Kashimawo, Ogochukwu Francis Osifo, Chidi Nkwocha, Peter Iyitor, Temi Abiwon, Adeola Adeleye, A Kadir La Ode, Anjola Ayo-Lawal, Kasiena Akpabio, Emame Edu, Chiemela Njoku, Bari J. Ballew, Cameron D. Palmer, Abdullahi Musa, Abdulrasheed M. Mujtaba, Abiodun Popoola, Abubakar M. Bello, Anthony Anyanwu, Ashiru Yusuf, G. E. Bozimo, Goddy Bassey, Hadiza Bala, Istifanus Bala Bosan, Jemimah Edah, Mutiu Jimoh, Kenneth Nwankwo, Olalekan Ojo, Marcus Inyama, Maryam Apanpa, M. Mustapha, Musa Ali-Gombe, Olubukola Ojo, Oludare Adeyemi, Samuel Ajayi, Sanusi Bala, Temitope Ojo, Usman Malami Aliyu, Yemi Raheem Raji, Zainab Tanko, Amina Mohammed, David Oladele, Muhammed Hamzat, Emmanuel I. Agaba, Emeka Nwankwo, Ifeoma Ulasi, Jonah Musa, Umeora Odidika, Omolola Salako, Oyekanmi Nashiru, Babatunde Lawal Salako, Colm O’Dushlaine, Abasi Ene–Obong - Nature Genetics 2022 cited by 63
- Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4
Authors: Pamela Sklar, Stephan Ripke, Laura J. Scott, Ole A. Andreassen, Sven Cichon, Nick Craddock, Howard J. Edenberg, John I. Nürnberger, Marcella Rietschel, Douglas Blackwood, Aiden Corvin, Matthew Flickinger, Weihua Guan, Morten Mattingsdal, Andrew McQuillin, Phoenix Kwan, Thomas F. Wienker, Mark J. Daly, Frank Dudbridge, Peter Holmans, Danyu Lin, Margit Burmeister, Tiffany A. Greenwood, Marian L. Hamshere, Pierandrea Muglia, Erin N. Smith, Peter P. Zandi, Caroline M. Nievergelt, R. Anne McKinney, Paul D. Shilling, Nicholas J. Schork, Cinnamon S. Bloss, Tatiana Foroud, Daniel L. Koller, Elliot S. Gershon, Chunyu Liu, Judith A. Badner, William A. Scheftner, William Lawson, Evaristus Nwulia, Maria Hipolito, William Coryell, John Rice, William Byerley, Francis J. McMahon, Thomas G. Schulze, Wade H. Berrettini, Falk W. Lohoff, James B. Potash, Pamela B. Mahon, Melvin G. McInnis, Sebastian Zöllner, Peng Zhang, David W. Craig, Szabocls Szelinger, Thomas B. Barrett, René Breuer, Sandra Meier, Jana Strohmaier, Stephanie H. Witt, Federica Tozzi, Anne Farmer, Peter McGuffin, John S. Strauss, Wei Xu, James L Kennedy, John B. Vincent, K. Matthews, Richard Day, Manuel A. R. Ferreira, Colm Ó'Dúshláine, Roy H. Perlis, Soumya Raychaudhuri, Douglas M. Ruderfer, Phil H Lee, Jordan W. Smoller, Jun Li, Devin Absher, William E. Bunney, Jack D. Barchas, Alan F. Schatzberg, Edward G. Jones, Fan Meng, Robert C. Thompson, Stanley J. Watson, Richard M. Myers, Huda Akil, Michael Boehnke, Kim Chambert, Jennifer L. Moran, Ed Scolnick, Srdjan Djurovic, Ingrid Melle, Gunnar Morken, Michael Gill, Derek W. Morris, Emma M. Quinn, Thomas W. Mühleisen, Franziska Degenhardt, Manuel Mattheisen and 72 more - Nature Genetics 2011 cited by 1,412
- Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry
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