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Adam E. Locke
Researcher at Washington University in St. Louis
Publications - 105
Citations - 16087
Adam E. Locke is an academic researcher from Washington University in St. Louis. The author has contributed to research in topics: Genome-wide association study & Exome sequencing. The author has an hindex of 35, co-authored 86 publications receiving 12473 citations. Previous affiliations of Adam E. Locke include University of Michigan & Emory University.
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Journal ArticleDOI
Interaction between the FTO gene, body mass index and depression: meta-analysis of 13701 individuals†
Margarita Rivera,Adam E. Locke,Tanguy Corre,Darina Czamara,Christiane Wolf,Ana Ching-López,Yuri Milaneschi,Stefan Kloiber,Sara Cohen-Woods,James Rucker,Katherine J. Aitchison,Sven Bergmann,Dorret I. Boomsma,Nicholas John Craddock,Michael Gill,Florian Holsboer,Jouke-Jan Hottenga,Ania Korszun,Zoltán Kutalik,Susanne Lucae,Wolfgang Maier,Ole Mors,Bertram Müller-Myhsok,Michael John Owen,Brenda W.J.H. Penninx,Martin Preisig,John P. Rice,Marcella Rietschel,F. Tozzi,Rudolf Uher,Peter Vollenweider,Gérard Waeber,Gonneke Willemsen,Ian W. Craig,Anne Farmer,Cathryn M. Lewis,Gerome Breen,Peter McGuffin +37 more
TL;DR: This meta-analysis provides additional support for a significant interaction between FTO, depression and BMI, indicating that depression increases the effect of FTO on BMI.
Posted ContentDOI
Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans
Jedidiah Carlson,Laura J. Scott,Adam E. Locke,Matthew Flickinger,Shawn Levy,Richard M. Myers,Michael Boehnke,Hyun Min Kang,Jun Li,Sebastian Zöllner +9 more
TL;DR: This work uses ∼36 million singleton variants from 3,560 whole-genome sequences to infer fine-scale patterns of mutation rate heterogeneity and provides the most refined portrait to date of the factors contributing to genome-wide variability of the human germline mutation rate.
Posted ContentDOI
Common genetic variants identify therapeutic targets for COVID-19 and individuals at high risk of severe disease
Julie E. 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 Maxwell,Spencer C. Knight,Xiaodong Bai,Harenda Guturu,Dylan Sun,Asher K. Haug Baltzell,Fabricio S. P. Kury,Joshua D. Backman,Ahna R. Girshick,Colm O'Dushlaine,Shannon R. McCurdy,Raghavendran Partha,Adam J. Mansfield,David A. Turissini,Alexander H. Li,Miao Zhang,Joelle Mbatchou,Kyoko Watanabe,Lauren Gurski,Shane McCarthy,Hyun Min Kang,Lee Dobbyn,Eli A. Stahl,Anurag Verma,Giorgio Sirugo,Marylyn D. Ritchie,Marcus B. Jones,Suganthi Balasubramanian,Katherine A. Siminovitch,William J Salerno,Alan R. Shuldiner,Daniel J. Rader,Tooraj Mirshahi,Adam E. Locke,Jonathan Marchini,John D. Overton,David J. Carey,Lukas Habegger,Michael N. Cantor,Kristin A. Rand,Eurie L. Hong,Jeffrey G. Reid,Catherine A. Ball,Aris Baras,Gonçalo R. Abecasis,Manuel A. R. Ferreira +58 more
TL;DR: Seven common genetic variants that modulate COVID-19 susceptibility and severity are identified, implicating IFNAR2, CCHCR1, TCF19, SLC6A20 and the hyaluronan pathway as potential therapeutic targets.
Journal ArticleDOI
Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia
Duncan S. Palmer,Daniel P. Howrigan,Sinéad B. Chapman,Rolf Adolfsson,Nicholas Bass,Douglas Blackwood,Marco P. Boks,Chia-Yen Chen,Claire Churchhouse,Aiden Corvin,Nicholas John Craddock,David Curtis,Arianna Di Florio,Faith Dickerson,Nelson B. Freimer,Fernando S. Goes,Xiaoming Jia,Ian Jones,Lisa Jones,Lina Jonsson,René S. Kahn,Mikael Landén,Adam E. Locke,Andrew M. McIntosh,Andrew McQuillin,Derek W. Morris,Michael Conlon O'Donovan,Roel A. Ophoff,Michael John Owen,Nancy L. Pedersen,Danielle Posthuma,Andreas Reif,Neil Risch,Catherine Schaefer,Laura J. Scott,Tarjinder Singh,Jordan W. Smoller,Matthew Solomonson,David St Clair,Eli A. Stahl,Annabel Vreeker,James T.R. Walters,Weiqing Wang,Nicholas A. Watts,R.T Yolken,Peter P. Zandi,Benjamin M. Neale +46 more
TL;DR: In this article , the authors report results from the Bipolar exome (BipEx) collaboration analysis of whole-exome sequencing of 13,933 patients with bipolar disorder matched with 14,422 controls, finding an excess of ultra-rare protein-truncating variants (PTVs) in patients with BD among genes under strong evolutionary constraint in both major BD subtypes.
Journal ArticleDOI
Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21
Tiffany Renee Oliver,Tiffany Renee Oliver,Stuart W. Tinker,Emily G. Allen,NaTasha D. Hollis,Adam E. Locke,Lora J. H. Bean,Reshmi Chowdhury,Ferdouse Begum,Mary L. Marazita,Vivian G. Cheung,Eleanor Feingold,Stephanie L. Sherman +12 more
TL;DR: Characteristics of maternal chromosomes 21 that exhibited multiple recombinant events on 21q are examined to determine whether additional risk factors or mechanisms are suggested and to better understand mechanisms that may underlie both age-related and nonage-related meiotic chromosome mal-segregation.