Publications:

A genome-wide association scan implicates DCHS2, RUNX2, GLI3, PAX1 and EDAR in human facial variation.

Nature Communications

Adhikari, Kaustubh K; Fuentes-Guajardo, Macarena M; Quinto-Sánchez, Mirsha M; Mendoza-Revilla, Javier J; Camilo Chacón-Duque, Juan J; Acuña-Alonzo, Victor V; Jaramillo, Claudia C; Arias, William W; Lozano, Rodrigo Barquera RB; Pérez, Gastón Macín GM; Gómez-Valdés, Jorge J; Villamil-Ramírez, Hugo H; Hunemeier, Tábita T; Ramallo, Virginia V; Silva de Cerqueira, Caio C CC; Hurtado, Malena M; Villegas, Valeria V; Granja, Vanessa V; Gallo, Carla C; Poletti, Giovanni G; Schuler-Faccini, Lavinia L; Salzano, Francisco M FM; Bortolini, Maria-Cátira MC; Canizales-Quinteros, Samuel S; Cheeseman, Michael M; Rosique, Javier J; Bedoya, Gabriel G; Rothhammer, Francisco F; Headon, Denis D; González-José, Rolando R; Balding, David D; Ruiz-Linares, Andrés A

Publication Date: 2016-05-19

Variant appearance in text: rs35565233

PubMed Link: 27193062

Variant Present in the following documents:

• ncomms11616-s1.pdf

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Association Between Dentin Matrix Protein 1 (rs10019009) Polymorphism and Ankylosing Spondylitis in a Chinese Han Population from Shandong Province.

Chinese Medical Journal

Liu, Jian-Min JM; Cui, Ya-Zhou YZ; Zhang, Geng-Lin GL; Zhou, Xiao-Yan XY; Pang, Jing-Xiang JX; Wang, Xue-Zheng XZ; Han, Jin-Xiang JX

Publication Date: 2016-03-20

Variant appearance in text: rs35565233

PubMed Link: 26960368

Variant Present in the following documents:

• CMJ-129-657.pdf

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Calcium Signaling Pathway Genes RUNX2 and CACNA1C Are Associated With Calcific Aortic Valve Disease.

Circulation. Cardiovascular Genetics

Guauque-Olarte, Sandra S; Messika-Zeitoun, David D; Droit, Arnaud A; Lamontagne, Maxime M; Tremblay-Marchand, Joël J; Lavoie-Charland, Emilie E; Gaudreault, Nathalie N; Arsenault, Benoit J BJ; Dubé, Marie-Pierre MP; Tardif, Jean-Claude JC; Body, Simon C SC; Seidman, Jonathan G JG; Boileau, Catherine C; Mathieu, Patrick P; Pibarot, Philippe P; Bossé, Yohan Y

Publication Date: 2015-12

Variant appearance in text: rs35565233

PubMed Link: 26553695

Variant Present in the following documents:

• Main text

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