Polygenic contribution to the relationship of loneliness and social isolation with schizophrenia.
Nature Communications
Andreu-Bernabeu, Álvaro Á; Díaz-Caneja, Covadonga M CM; Costas, Javier J; De Hoyos, Lucía L; Stella, Carol C; Gurriarán, Xaquín X; Alloza, Clara C; Fañanás, Lourdes L; Bobes, Julio J; González-Pinto, Ana A; Crespo-Facorro, Benedicto B; Martorell, Lourdes L; Vilella, Elisabet E; Muntané, Gerard G; Nacher, Juan J; Molto, María Dolores MD; Aguilar, Eduardo Jesús EJ; Parellada, Mara M; Arango, Celso C; González-Peñas, Javier J
Genome-wide association analyses of post-traumatic stress disorder and its symptom subdomains in the Million Veteran Program.
Nature Genetics
Stein, Murray B MB; Levey, Daniel F DF; Cheng, Zhongshan Z; Wendt, Frank R FR; Harrington, Kelly K; Pathak, Gita A GA; Cho, Kelly K; Quaden, Rachel R; Radhakrishnan, Krishnan K; Girgenti, Matthew J MJ; Ho, Yuk-Lam Anne YA; Posner, Daniel D; Aslan, Mihaela M; Duman, Ronald S RS; Zhao, Hongyu H; , ; , ; Polimanti, Renato R; Concato, John J; Gelernter, Joel J
Phenome-wide investigation of health outcomes associated with genetic predisposition to loneliness.
Human Molecular Genetics
Abdellaoui, Abdel A; Sanchez-Roige, Sandra S; Sealock, Julia J; Treur, Jorien L JL; Dennis, Jessica J; Fontanillas, Pierre P; Elson, Sarah S; , ; Nivard, Michel G MG; Ip, Hill Fung HF; van der Zee, Matthijs M; Baselmans, Bart M L BML; Hottenga, Jouke Jan JJ; Willemsen, Gonneke G; Mosing, Miriam M; Lu, Yi Y; Pedersen, Nancy L NL; Denys, Damiaan D; Amin, Najaf N; M van Duijn, Cornelia C; Szilagyi, Ingrid I; Tiemeier, Henning H; Neumann, Alexander A; Verweij, Karin J H KJH; Cacioppo, Stephanie S; Cacioppo, John T JT; Davis, Lea K LK; Palmer, Abraham A AA; Boomsma, Dorret I DI
Dual molecular diagnosis contributes to atypical Prader-Willi phenotype in monozygotic twins.
American Journal Of Medical Genetics. Part A
Jehee, Fernanda S FS; de Oliveira, Valdirene T VT; Gurgel-Giannetti, Juliana J; Pietra, Rafaella X RX; Rubatino, Fernando V M FVM; Carobin, Natália V NV; Vianna, Gabrielle S GS; de Freitas, Mariana L ML; Fernandes, Karla S KS; Ribeiro, Beatriz S V BSV; Brüggenwirth, Hennie T HT; Ali-Amin, Roza R; , ; White, Janson J JJ; Akdemir, Zeynep C ZC; Jhangiani, Shalini N SN; Gibbs, Richard A RA; Lupski, James R JR; Varela, Monica C MC; Koiffmann, Célia C; Rosenberg, Carla C; Carvalho, Cláudia M B CMB
Generation of a High Number of Healthy Erythroid Cells from Gene-Edited Pyruvate Kinase Deficiency Patient-Specific Induced Pluripotent Stem Cells.
Stem Cell Reports
Garate, Zita Z; Quintana-Bustamante, Oscar O; Crane, Ana M AM; Olivier, Emmanuel E; Poirot, Laurent L; Galetto, Roman R; Kosinski, Penelope P; Hill, Collin C; Kung, Charles C; Agirre, Xabi X; Orman, Israel I; Cerrato, Laura L; Alberquilla, Omaira O; Rodriguez-Fornes, Fatima F; Fusaki, Noemi N; Garcia-Sanchez, Felix F; Maia, Tabita M TM; Ribeiro, Maria L ML; Sevilla, Julian J; Prosper, Felipe F; Jin, Shengfang S; Mountford, Joanne J; Guenechea, Guillermo G; Gouble, Agnes A; Bueren, Juan A JA; Davis, Brian R BR; Segovia, Jose C JC
Comprehensive assessment of genetic variants within TCF4 in Fuchs' endothelial corneal dystrophy.
Investigative Ophthalmology & Visual Science
Wieben, Eric D ED; Aleff, Ross A RA; Eckloff, Bruce W BW; Atkinson, Elizabeth J EJ; Baheti, Saurabh S; Middha, Sumit S; Brown, William L WL; Patel, Sanjay V SV; Kocher, Jean-Pierre A JP; Baratz, Keith H KH