Jessica X. Chong, Ph.D.

Affiliations: 
2012 Human Genetics University of Chicago, Chicago, IL 
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"Jessica Chong"
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Carole Ober grad student 2012 Chicago
 (Studies of autosomal recessive disease mutations in a founder population.)
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Publications

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Chong JX, Caputo V, Phelps IG, et al. (2016) Recessive Inactivating Mutations in TBCK, Encoding a Rab GTPase-Activating Protein, Cause Severe Infantile Syndromic Encephalopathy. American Journal of Human Genetics
Emond MJ, Louie T, Emerson J, et al. (2015) Correction: Exome Sequencing of Phenotypic Extremes Identifies CAV2 and TMC6 as Interacting Modifiers of Chronic Pseudomonas aeruginosa Infection in Cystic Fibrosis. Plos Genetics. 11: e1005424
Emond MJ, Louie T, Emerson J, et al. (2015) Exome Sequencing of Phenotypic Extremes Identifies CAV2 and TMC6 as Interacting Modifiers of Chronic Pseudomonas aeruginosa Infection in Cystic Fibrosis. Plos Genetics. 11: e1005273
Chong JX, Burrage LC, Beck AE, et al. (2015) Autosomal-Dominant Multiple Pterygium Syndrome Is Caused by Mutations in MYH3. American Journal of Human Genetics. 96: 841-9
Chong JX, McMillin MJ, Shively KM, et al. (2015) De novo mutations in NALCN cause a syndrome characterized by congenital contractures of the limbs and face, hypotonia, and developmental delay. American Journal of Human Genetics. 96: 462-73
Chong JX, Buckingham KJ, Jhangiani SN, et al. (2015) The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities American Journal of Human Genetics
Rehman AU, Santos-Cortez RL, Drummond MC, et al. (2014) Challenges and solutions for gene identification in the presence of familial locus heterogeneity. European Journal of Human Genetics : Ejhg
Campbell CD, Mohajeri K, Malig M, et al. (2014) Whole-genome sequencing of individuals from a founder population identifies candidate genes for asthma. Plos One. 9: e104396
Tabor HK, Auer PL, Jamal SM, et al. (2014) Pathogenic variants for Mendelian and complex traits in exomes of 6,517 European and African Americans: implications for the return of incidental results. American Journal of Human Genetics. 95: 183-93
Anderson RL, Murray K, Chong JX, et al. (2014) Disclosure of genetic research results to members of a founder population. Journal of Genetic Counseling. 23: 984-91
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