Kwame Anyane-Yeboa

7PUBLICATIONS
56CO-AUTHORS
Developmental genetics (incl. sex determination)Major global burdens of diseaseCancer geneticsMedical infection agents (incl. prions)Neurogenetics
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Publications (7)

|Jun 28, 2023
Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, genotype-phenotype correlations and common mechanisms.

Maninder Kaur, Justin Blair, Batsal Devkota

|Oct 08, 2022
Assessment of the beliefs, needs, and expectations for genetic counseling of patients with hypermobile Ehlers-Danlos syndrome.

Priyanka Ahimaz, Tamar Kramer, Pooja Swaroop

|Jun 30, 2022
Brain Abnormalities in Patients with Germline Variants in H3F3: Novel Imaging Findings and Neurologic Symptoms Beyond Somatic Variants and Brain Tumors.

C A P F Alves, O Sherbini, F D'Arco

|Feb 11, 2022
Phenotypic spectrum of the recurrent TRPM3 p.(Val837Met) substitution in seven individuals with global developmental delay and hypotonia.

Matthew A Lines, Paula Goldenberg, Ashley Wong

|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

|Apr 24, 2019
Homozygous noncanonical splice variant in LSM1 in two siblings with multiple congenital anomalies and global developmental delay.

Volkan Okur, Charles A LeDuc, Edwin Guzman

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Frequent Collaborators

2 joint publications

Anya Revah-Politi

1 joint publications

C A P F Alves

1 joint publications

D Steel

1 joint publications

M A Kurian