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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 2 (of 2 Records)

Query Trace: Disease and SLITRK1[original query]
Overrepresentation of rare variants in a specific ethnic group may confuse interpretation of association analyses.
Human molecular genetics 2006 Nov 15 (22): 3324-8.
Keen-Kim Dianne, Mathews Carol A, Reus Victor I, Lowe Thomas L, Herrera Luis Diego, Budman Cathy L, Gross-Tsur Varda, Pulver Ann E, Bruun Ruth D, Erenberg Gerald, Naarden Allan, Sabatti Chiara, Freimer Nelson
Targeted Re-Sequencing Approach of Candidate Genes Implicates Rare Potentially Functional Variants in Tourette Syndrome Etiology.
Frontiers in neuroscience 2016 10 428.
Alexander John, Potamianou Hera, Xing Jinchuan, Deng Li, Karagiannidis Iordanis, Tsetsos Fotis, Drineas Petros, Tarnok Zsanett, Rizzo Renata, Wolanczyk Tomasz, Farkas Luca, Nagy Peter, Szymanska Urszula, Androutsos Christos, Tsironi Vaia, Koumoula Anastasia, Barta Csaba, , Sandor Paul, Barr Cathy L, Tischfield Jay, Paschou Peristera, Heiman Gary A, Georgitsi Mariant
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