Labile carbon limits late winter microbial activity near Arctic treeline

por Patrick F. Sullivan, Madeline C. Stokes, Cameron K. McMillan, Michael N. Weintraub
Publicado 2020

mTADA is a framework for identifying risk genes from de novo mutations in multiple traits

por Tan-Hoang Nguyen, Amanda Dobbyn, Ruth C. Brown, Brien P. Riley, Joseph D. Buxbaum, Dalila Pinto, Shaun M. Purcell, Patrick F. Sullivan, Xin He, Eli A. Stahl
Publicado 2020

Genetic variation in 117 myelination-related genes in schizophrenia: Replication of association to lipid biosynthesis genes

por Tomasz Stokowy, Tatiana Polushina, Ida E. Sønderby, Robert Karlsson, Sudheer Giddaluru, Stephanie Le Hellard, Sarah E. Bergen, Patrick F. Sullivan, Ole A. Andreassen, Srdjan Djurovic, Christina M. Hultman, Vidar M. Steen
Publicado 2018

Non-coding variability at the APOE locus contributes to the Alzheimer’s risk

por Xiaopu Zhou, Yu Chen, Kin Y. Mok, Timothy C. Y. Kwok, Vincent C. T. Mok, Qihao Guo, Fanny C. Ip, Yuewen Chen, Nandita Mullapudi, Alzheimer’s Disease Neuroimaging Initiative, Paola Giusti-Rodríguez, Patrick F. Sullivan, John Hardy, Amy K. Y. Fu, Yun Li, Nancy Y. Ip
Publicado 2019

Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia

por Matthew Halvorsen, Ruth Huh, Nikolay Oskolkov, Jia Wen, Sergiu Netotea, Paola Giusti-Rodriguez, Robert Karlsson, Julien Bryois, Björn Nystedt, Adam Ameur, Anna K. Kähler, NaEshia Ancalade, Martilias Farrell, James J. Crowley, Yun Li, Patrik K. E. Magnusson, Ulf Gyllensten, Christina M. Hultman, Patrick F. Sullivan, Jin P. Szatkiewicz
Publicado 2020

PCM1 is necessary for focal ciliary integrity and is a candidate for severe schizophrenia

por Tanner O. Monroe, Melanie E. Garrett, Maria Kousi, Ramona M. Rodriguiz, Sungjin Moon, Yushi Bai, Steven C. Brodar, Karen L. Soldano, Jeremiah Savage, Thomas F. Hansen, Donna M. Muzny, Richard A. Gibbs, Lawrence Barak, Patrick F. Sullivan, Allison E. Ashley-Koch, Akira Sawa, William C. Wetsel, Thomas Werge, Nicholas Katsanis
Publicado 2020

Genome-wide association study implicates chromosome 9q21.31 as a susceptibility locus for asthma in mexican children.

por Dana B Hancock, Isabelle Romieu, Min Shi, Juan-Jose Sienra-Monge, Hao Wu, Grace Y Chiu, Huiling Li, Blanca Estela del Rio-Navarro, Saffron A G Willis-Owen, Scott T Weiss, Benjamin A Raby, Hong Gao, Celeste Eng, Rocio Chapela, Esteban G Burchard, Hua Tang, Patrick F Sullivan, Stephanie J London
Publicado 2009

Evaluation of chromatin accessibility in prefrontal cortex of individuals with schizophrenia

por Julien Bryois, Melanie E. Garrett, Lingyun Song, Alexias Safi, Paola Giusti-Rodriguez, Graham D. Johnson, Annie W. Shieh, Alfonso Buil, John F. Fullard, Panos Roussos, Pamela Sklar, Schahram Akbarian, Vahram Haroutunian, Craig A. Stockmeier, Gregory A. Wray, Kevin P. White, Chunyu Liu, Timothy E. Reddy, Allison Ashley-Koch, Patrick F. Sullivan, Gregory E. Crawford
Publicado 2018

Addendum: Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways

por David M. Howard, Mark J. Adams, Masoud Shirali, Toni-Kim Clarke, Riccardo E. Marioni, Gail Davies, Jonathan R. I. Coleman, Clara Alloza, Xueyi Shen, Miruna C. Barbu, Eleanor M. Wigmore, Jude Gibson, Saskia P. Hagenaars, Cathryn M. Lewis, Joey Ward, Daniel J. Smith, Patrick F. Sullivan, Chris S. Haley, Gerome Breen, Ian J. Deary, Andrew M. McIntosh
Publicado 2018

Author Correction: Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways

por David M. Howard, Mark J. Adams, Masoud Shirali, Toni-Kim Clarke, Riccardo E. Marioni, Gail Davies, Jonathan R. I. Coleman, Clara Alloza, Xueyi Shen, Miruna C. Barbu, Eleanor M. Wigmore, Jude Gibson, 23andMe Research Team, Saskia P. Hagenaars, Cathryn M. Lewis, Joey Ward, Daniel J. Smith, Patrick F. Sullivan, Chris S. Haley, Gerome Breen, Ian J. Deary, Andrew M. McIntosh
Publicado 2021

Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways

por David M. Howard, Mark J. Adams, Masoud Shirali, Toni-Kim Clarke, Riccardo E. Marioni, Gail Davies, Jonathan R. I. Coleman, Clara Alloza, Xueyi Shen, Miruna C. Barbu, Eleanor M. Wigmore, Jude Gibson, 23andMe Research Team, Saskia P. Hagenaars, Cathryn M. Lewis, Joey Ward, Daniel J. Smith, Patrick F. Sullivan, Chris S. Haley, Gerome Breen, Ian J. Deary, Andrew M. McIntosh
Publicado 2018