Publications:

A systematic review of common genetic variation and biological pathways in autism spectrum disorder.

Bmc Neuroscience

Rodriguez-Gomez, Diego Alejandro DA; Garcia-Guaqueta, Danna Paola DP; Charry-Sánchez, Jesús David JD; Sarquis-Buitrago, Elias E; Blanco, Mariana M; Velez-van-Meerbeke, Alberto A; Talero-Gutiérrez, Claudia C

Publication Date: 2021-10-09

Variant appearance in text: rs12603582

PubMed Link: 34627165

Variant Present in the following documents:

• 12868_2021_662_MOESM1_ESM.xlsx, sheet 1

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Imaging genetics in neurodevelopmental psychopathology.

American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication Of The International Society Of Psychiatric Genetics

Klein, Marieke M; van Donkelaar, Marjolein M; Verhoef, Ellen E; Franke, Barbara B

Publication Date: 2017-07

Variant appearance in text: rs12603582

PubMed Link: 29984470

Variant Present in the following documents:

• Main text

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Genetic overlap between multiple sclerosis and several cardiovascular disease risk factors.

Multiple Sclerosis (Houndmills, Basingstoke, England)

Wang, Yunpeng Y; Bos, Steffan D SD; Harbo, Hanne F HF; Thompson, Wesley K WK; Schork, Andrew J AJ; Bettella, Francesco F; Witoelar, Aree A; Lie, Benedicte A BA; Li, Wen W; McEvoy, Linda K LK; Djurovic, Srdjan S; Desikan, Rahul S RS; Dale, Anders M AM; Andreassen, Ole A OA

Publication Date: 2016-12

Variant appearance in text: rs12603582

PubMed Link: 26920376

Variant Present in the following documents:

• Main text

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Integrin β3 Haploinsufficiency Modulates Serotonin Transport and Antidepressant-Sensitive Behavior in Mice.

Neuropsychopharmacology : Official Publication Of The American College Of Neuropsychopharmacology

Mazalouskas, Matthew M; Jessen, Tammy T; Varney, Seth S; Sutcliffe, James S JS; Veenstra-VanderWeele, Jeremy J; Cook, Edwin H EH; Carneiro, Ana M D AM

Publication Date: 2015-07

Variant appearance in text: rs12603582

PubMed Link: 25684064

Variant Present in the following documents:

• Main text

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Family-based association study of ITGB3 in autism spectrum disorder and its endophenotypes.

European Journal Of Human Genetics : Ejhg

Napolioni, Valerio V; Lombardi, Federica F; Sacco, Roberto R; Curatolo, Paolo P; Manzi, Barbara B; Alessandrelli, Riccardo R; Militerni, Roberto R; Bravaccio, Carmela C; Lenti, Carlo C; Saccani, Monica M; Schneider, Cindy C; Melmed, Raun R; Pascucci, Tiziana T; Puglisi-Allegra, Stefano S; Reichelt, Karl-Ludvig KL; Rousseau, Francis F; Lewin, Patricia P; Persico, Antonio M AM

Publication Date: 2011-03

Variant appearance in text: rs12603582

PubMed Link: 21102624

Variant Present in the following documents:

• Main text

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