Results 111 to 120 of about 1,621 (139)

Rare de novo damaging DNA variants are enriched in attention-deficit/hyperactivity disorder and implicate risk genes. [PDF]

Nat Commun
Olfson E, Farhat LC, Liu W, Vitulano LA, Zai G, Lima MO, Parent J, Polanczyk GV, Cappi C, Kennedy JL, Fernandez TV.   +10 more
europepmc   +1 more source

Proteomics of neurodegenerative diseases: analysis of human post-mortem brain. [PDF]

J Neurochem, 2019
Li KW, Ganz AB, Smit AB.
europepmc   +1 more source

Shades of white: The Petunia long corolla tube clade evolutionary history. [PDF]

Genet Mol Biol
Backes A, Turchetto C, Mäder G, Segatto ALA, Bonatto SL, Freitas LB.   +5 more
europepmc   +1 more source

Estrogen activates Alzheimer's disease genes. [PDF]

Alzheimers Dement (N Y), 2019
Ratnakumar A, Zimmerman SE, Jordan BA, Mar JC.   +3 more
europepmc   +1 more source

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders. [PDF]

Am J Hum Genet, 2014
Pinto D, Delaby E, Merico D, Barbosa M, Merikangas A, Klei L, Thiruvahindrapuram B, Xu X, Ziman R, Wang Z, Vorstman JA, Thompson A, Regan R, Pilorge M, Pellecchia G, Pagnamenta AT, Oliveira B, Marshall CR, Magalhaes TR, Lowe JK, Howe JL, Griswold AJ, Gilbert J, Duketis E, Dombroski BA, De Jonge MV, Cuccaro M, Crawford EL, Correia CT, Conroy J, Conceição IC, Chiocchetti AG, Casey JP, Cai G, Cabrol C, Bolshakova N, Bacchelli E, Anney R, Gallinger S, Cotterchio M, Casey G, Zwaigenbaum L, Wittemeyer K, Wing K, Wallace S, van Engeland H, Tryfon A, Thomson S, Soorya L, Rogé B, Roberts W, Poustka F, Mouga S, Minshew N, McInnes LA, McGrew SG, Lord C, Leboyer M, Le Couteur AS, Kolevzon A, Jiménez González P, Jacob S, Holt R, Guter S, Green J, Green A, Gillberg C, Fernandez BA, Duque F, Delorme R, Dawson G, Chaste P, Café C, Brennan S, Bourgeron T, Bolton PF, Bölte S, Bernier R, Baird G, Bailey AJ, Anagnostou E, Almeida J, Wijsman EM, Vieland VJ, Vicente AM, Schellenberg GD, Pericak-Vance M, Paterson AD, Parr JR, Oliveira G, Nurnberger JI, Monaco AP, Maestrini E, Klauck SM, Hakonarson H, Haines JL, Geschwind DH, Freitag CM, Folstein SE, Ennis S, Coon H, Battaglia A, Szatmari P, Sutcliffe JS, Hallmayer J, Gill M, Gill M, Cook EH, Buxbaum JD, Devlin B, Gallagher L, Betancur C, Scherer SW.   +112 more
europepmc   +1 more source

Side Effects and Behavioral Outcomes Following High-Dose Carnitine Supplementation Among Young Males With Autism Spectrum Disorder: A Pilot Study. [PDF]

Glob Pediatr Health, 2019
Goin-Kochel RP, Scaglia F, Schaaf CP, Berry LN, Dang D, Nowel KP, Laakman AL, Dowell LR, Minard CG, Loh A, Beaudet AL.   +10 more
europepmc   +1 more source

Joint analysis of psychiatric disorders increases accuracy of risk prediction for schizophrenia, bipolar disorder, and major depressive disorder. [PDF]

Am J Hum Genet, 2015
Maier R, Moser G, Chen GB, Ripke S, Cross-Disorder Working Group of the Psychiatric Genomics Consortium, Coryell W, Potash JB, Scheftner WA, Shi J, Weissman MM, Hultman CM, Landén M, Levinson DF, Kendler KS, Smoller JW, Wray NR, Lee SH.   +16 more
europepmc   +1 more source

Lexical decision as an endophenotype for reading comprehension: an exploration of an association. [PDF]

Dev Psychopathol, 2012
Naples A, Katz L, Grigorenko EL.
europepmc   +1 more source

Efficient Estimation of Realized Kinship from Single Nucleotide Polymorphism Genotypes. [PDF]

Genetics, 2017
Wang B, Sverdlov S, Thompson E.
europepmc   +1 more source

Comparison of marker types and map assumptions using Markov chain Monte Carlo-based linkage analysis of COGA data. [PDF]

BMC Genet, 2005
Sieh W, Basu S, Fu AQ, Rothstein JH, Scheet PA, Stewart WC, Sung YJ, Thompson EA, Wijsman EM.   +8 more
europepmc   +1 more source