Ariel F Martinez

ORCID

Publication Activity (10 Years)

Years Active: 2018-2020
Publications (10 Years): 6

Top Venues

American journal of medical genetics. Part C, Seminars in medical genetics

Translational psychiatry

Genetics in medicine : official journal of the American College of Medical Genetics

National Human Genome Research Institute

This page only lists publications with an associated author ORCID identifier.

Affiliation History

National Human Genome Research Institute Jun 01 2010

United States

Biologist :: Medical Genetics Branch

Publications

Marcela Henriquez-Henriquez, Maria T Acosta, Ariel F Martinez, Jorge Iván Vélez, Francisco Lopera, David A Pineda, Juan D Palacio, Teresa Quiroga, Tilla S Worgall, Richard J Deckelbaum, Claudio Mastronardi, Brooke S G Molina, null null, Mauricio Arcos-Burgos, Maximilian Muenke
Mutations in sphingolipid metabolism genes are associated with ADHD. Translational psychiatry 10 (1) (2020)
Tommy Hu, Paul S Kruszka, Ariel F Martinez, Jeffrey E Ming, Emily K Shabason, Manu S Raam, Tamim H Shaikh, Daniel E Pineda-Alvarez, Maximilian Muenke
Cytogenetics and holoprosencephaly: A chromosomal microarray study of 222 individuals with holoprosencephaly. American journal of medical genetics. Part C, Seminars in medical genetics 178 (2) (2019)
Mauricio Arcos-Burgos, Jorge Iván Vélez, Ariel F Martinez, Marta Ribases, Josep A Ramos-Quiroga, Cristina Sánchez-Mora, Vanesa Richarte, Carlos Roncero, Bru Cormand, Noelia Fernández-Castillo, Miguel Casas, Francisco Lopera, David A Pineda, Juan D Palacio, Johan E Acosta-López, Martha L Cervantes-Henriquez, Manuel G Sánchez-Rojas, Pedro J Puentes-Rozo, Brooke S G Molina, null null, Margaret T Boden, Deeann Wallis, Brett Lidbury, Saul Justin Newman, Simon Easteal, James Swanson, Hardip Patel, Nora D Volkow, Maria T Acosta, Francisco X Castellanos, Jose De Leon, Claudio A Mastronardi, Maximilian Muenke
ADGRL3 (LPHN3) variants predict substance use disorder. Translational psychiatry 9 (1) (2019)
Karin Weiss, Hayley P Lazar, Alina Kurolap, Ariel F Martinez, Tamar Paperna, Lior Cohen, Marie F Smeland, Sandra Whalen, Solveig Heide, Boris Keren, Pauline Terhal, Melita Irving, Motoki Takaku, John D Roberts, Robert M Petrovich, Samantha A Schrier Vergano, Amy Kenney, Hanne Hove, Elizabeth DeChene, Shane C Quinonez, Estelle Colin, Alban Ziegler, Melissa Rumple, Mahim Jain, Danielle C Monteil, Elizabeth R Roeder, Kimberly Nugent, Arie van Haeringen, Michael Gambello, Avni Santani, Līvija Medne, Bryan Krock, Cara M Skraban, Elaine H Zackai, Holly A Dubbs, Thomas Smol, Jamal Ghoumid, Michael J Parker, Michael Wright, Peter D Turnpenny, Jill Clayton-Smith, Kay Metcalfe, Hitoshi Kurumizaka, Bruce D Gelb, Hagit Baris Feldman, Philippe M Campeau, Maximilian Muenke, Paul A Wade, Katherine Lachlan
The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype-phenotype correlations, and molecular basis. Genetics in medicine : official journal of the American College of Medical Genetics 22 (2) (2019)
Paul S Kruszka, Ariel F Martinez, Maximilian Muenke
Molecular testing in holoprosencephaly. American journal of medical genetics. Part C, Seminars in medical genetics 178 (2) (2018)
Ariel F Martinez, Paul S Kruszka, Maximilian Muenke
Extracephalic manifestations of nonchromosomal, nonsyndromic holoprosencephaly. American journal of medical genetics. Part C, Seminars in medical genetics 178 (2) (2018)

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Publication Activity (10 Years)

Top Topics

Top Venues

Ariel F Martinez