Anya Revah-Politi

5PUBLICATIONS
19CO-AUTHORS
Developmental genetics (incl. sex determination)NeurogeneticsEpigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)
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Publications (5)

|Jul 31, 2021
ZTTK syndrome: Clinical and molecular findings of 15 cases and a review of the literature.

Sulagna Tina Kushary, Anya Revah-Politi, Subit Barua

|Jun 11, 2021
Genetic testing in individuals with cerebral palsy.

Halie J May, Jennifer A Fasheun, Jennifer M Bain

|Oct 07, 2018
Heterozygous loss-of-function variants of MEIS2 cause a triad of palatal defects, congenital heart defects, and intellectual disability.

Rosalind Verheije, Gabriel S Kupchik, Bertrand Isidor

|Sep 09, 2018
Refining the phenotype associated with GNB1 mutations: Clinical data on 18 newly identified patients and review of the literature.

Parisa Hemati, Anya Revah-Politi, Haim Bassan

|Sep 24, 2017
Loss-of-function variants in NFIA provide further support that NFIA is a critical gene in 1p32-p31 deletion syndrome: A four patient series.

Anya Revah-Politi, Mythily Ganapathi, Louise Bier

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Frequent Collaborators

2 joint publications

Kwame Anyane-Yeboa

1 joint publications

Parisa Hemati

1 joint publications

Gunnar Houge

1 joint publications

Bruce D Gelb