Mersedeh Rohanizadegan

Medical Genetics

3400 Civic Center Boulevard
West Pavilion, 3rd Floor
Philadelphia, PA 19104

Last Updated: 09/26/2026

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Found 19 publications

Practice-Based Insights into Adult Genetics: High Diagnostic Yield, Demographic Determinants, and Patterns of Test Utilization in Over 7,000 Patients.

Practice-Based Insights into Adult Genetics: High Diagnostic Yield, Demographic Determinants, and Patterns of Test Utilization in Over 7,000 Patients.

Journal: medRxiv : the preprint server for health sciences

Published: November 24, 2025

Assessment of barriers to pancreatic cancer surveillance in high-risk individuals.

Assessment of barriers to pancreatic cancer surveillance in high-risk individuals.

Journal: Journal of genetic counseling

Published: July 16, 2025

Pathogenic Germline Variants in Patients With Metaplastic Breast Cancer.

Pathogenic Germline Variants in Patients With Metaplastic Breast Cancer.

Journal: JAMA network open

Published: February 18, 2025

Prevalence and Distribution of Unexpected Actionable Germline Pathogenic Variants Identified on Broad-Based Multigene Panel Testing Among Patients With Cancer.

Prevalence and Distribution of Unexpected Actionable Germline Pathogenic Variants Identified on Broad-Based Multigene Panel Testing Among Patients With Cancer.

Journal: JCO precision oncology

Published: December 12, 2024

Correction: Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlations.

Correction: Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlations.

Journal: European journal of human genetics : EJHG

Published: September 10, 2024

Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlations.

Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlations.

Journal: European journal of human genetics : EJHG

Published: January 30, 2024

Author Correction: A biallelic multiple nucleotide length polymorphism explains functional causality at 5p15.33 prostate cancer risk locus.

Author Correction: A biallelic multiple nucleotide length polymorphism explains functional causality at 5p15.33 prostate cancer risk locus.

Journal: Nature communications

Published: October 19, 2023

A biallelic multiple nucleotide length polymorphism explains functional causality at 5p15.33 prostate cancer risk locus.

A biallelic multiple nucleotide length polymorphism explains functional causality at 5p15.33 prostate cancer risk locus.

Journal: Nature communications

Published: March 29, 2021

Genetic diagnoses and associated anomalies in fetuses prenatally diagnosed with esophageal atresia.

Genetic diagnoses and associated anomalies in fetuses prenatally diagnosed with esophageal atresia.

Journal: American journal of medical genetics. Part A

Published: January 13, 2020

The tale of two genes: from next-generation sequencing to phenotype.

The tale of two genes: from next-generation sequencing to phenotype.

Journal: Cold Spring Harbor molecular case studies

Published: October 16, 2019

Misidentification of MLL3 and other mutations in cancer due to highly homologous genomic regions.

Misidentification of MLL3 and other mutations in cancer due to highly homologous genomic regions.

Journal: Leukemia & lymphoma

Published: July 11, 2019

Genomic Mismatch at LIMS1 Locus and Kidney Allograft Rejection.

Genomic Mismatch at LIMS1 Locus and Kidney Allograft Rejection.

Journal: The New England journal of medicine

Published: May 16, 2019

Showing 1-12 of 19

Last Updated: 09/26/2026