Mir Reza Bekheirnia

4PUBLICATIONS
27CO-AUTHORS
Obstetrics and gynaecologyEpigenetics (incl. genome methylation and epigenomics)Developmental genetics (incl. sex determination)Gene expression (incl. microarray and other genome-wide approaches)
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Publications (4)

|Aug 14, 2026
Opportunities for renal genetic evaluation among pregnant patients with kidney disease.

|Aug 05, 2025
Paternal UPD (15) With Disease-Causing Mutation and Small Supernumerary Ring Chromosome 15: A Case Report.

David Lee Curtis, Nasim Bekheirnia, Lorraine Potocki

|Jul 03, 2019
DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract.

Alexandria T M Blackburn, Nasim Bekheirnia, Vanessa C Uma

|Sep 23, 2016
Whole-exome sequencing in the molecular diagnosis of individuals with congenital anomalies of the kidney and urinary tract and identification of a new causative gene.

Mir Reza Bekheirnia, Nasim Bekheirnia, Matthew N Bainbridge

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Frequent Collaborators

2 joint publications

Nasim Bekheirnia

2 joint publications

Dolores J Lamb

2 joint publications

Jill A Rosenfeld

1 joint publications

Likhita Nandigam