Publications:

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CADM2 is implicated in impulsive personality and numerous other traits by genome- and phenome-wide association studies in humans and mice.

Translational Psychiatry

Sanchez-Roige, Sandra S; Jennings, Mariela V MV; Thorpe, Hayley H A HHA; Mallari, Jazlene E JE; van der Werf, Lieke C LC; Bianchi, Sevim B SB; Huang, Yuye Y; Lee, Calvin C; Mallard, Travis T TT; Barnes, Samuel A SA; Wu, Jin Yi JY; Barkley-Levenson, Amanda M AM; Boussaty, Ely C EC; Snethlage, Cedric E CE; Schafer, Danielle D; Babic, Zeljana Z; Winters, Boyer D BD; Watters, Katherine E KE; Biederer, Thomas T; , ; Mackillop, James J; Stephens, David N DN; Elson, Sarah L SL; Fontanillas, Pierre P; Khokhar, Jibran Y JY; Young, Jared W JW; Palmer, Abraham A AA

Publication Date: 2023-05-12

Variant appearance in text: rs936146

PubMed Link: 37173343

Variant Present in the following documents:

• 41398_2023_2453_MOESM2_ESM.xlsx, sheet 9
• 41398_2023_2453_MOESM2_ESM.xlsx, sheet 23

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Identifying interactive biological pathways associated with reading disability.

Brain And Behavior

Lancaster, Hope Sparks HS; Liu, Xiaonan X; Dinu, Valentin V; Li, Jing J

Publication Date: 2020-08

Variant appearance in text: rs936146

PubMed Link: 32596987

Variant Present in the following documents:

• Main text
• BRB3-10-e01735.pdf

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Neuroimaging genetics studies of specific reading disability and developmental language disorder: A review.

Language And Linguistics Compass

Landi, Nicole N; Perdue, Meaghan M

Publication Date: 2019-09

Variant appearance in text: rs936146

PubMed Link: 31844423

Variant Present in the following documents:

• Main text

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Dyslexia risk variant rs600753 is linked with dyslexia-specific differential allelic expression of DYX1C1.

Genetics And Molecular Biology

Müller, Bent B; Boltze, Johannes J; Czepezauer, Ivonne I; Hesse, Volker V; , ; Wilcke, Arndt A; Kirsten, Holger H

Publication Date: 2018

Variant appearance in text: rs936146

PubMed Link: 29473935

Variant Present in the following documents:

• 1415-4757-GMB-41-01-2017-0165-s002.pdf

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Imaging genetics of FOXP2 in dyslexia.

European Journal Of Human Genetics : Ejhg

Wilcke, Arndt A; Ligges, Carolin C; Burkhardt, Jana J; Alexander, Michael M; Wolf, Christiane C; Quente, Elfi E; Ahnert, Peter P; Hoffmann, Per P; Becker, Albert A; Müller-Myhsok, Bertram B; Cichon, Sven S; Boltze, Johannes J; Kirsten, Holger H

Publication Date: 2012-02

Variant appearance in text: rs936146

PubMed Link: 21897444

Variant Present in the following documents:

• Main text

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Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample.

Journal Of Neurodevelopmental Disorders

Peter, Beate B; Raskind, Wendy H WH; Matsushita, Mark M; Lisowski, Mark M; Vu, Tiffany T; Berninger, Virginia W VW; Wijsman, Ellen M EM; Brkanac, Zoran Z

Publication Date: 2011-03

Variant appearance in text: rs936146

PubMed Link: 21484596

Variant Present in the following documents:

• Main text
• 11689_2010_Article_9065.pdf

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