Nuriye Sahin‐Hodoglugil

University of California, San Francisco — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

12h-index666citations32works3.72yr avg
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Research Topics

Genomics and Rare Diseases(13), Prenatal Screening and Diagnostics(10), Adolescent Sexual and Reproductive Health(6), BRCA gene mutations in cancer(5), HIV/AIDS Research and Interventions(4)

Publications32 total

Genetic diseases underlying a spectrum of fetal effusions
American Journal of Obstetrics and Gynecology·2025· 6 citedOpen Access
Genomic sequencing in diverse and underserved pediatric populations: Parent perspectives on understanding, uncertainty, psychosocial impact, and personal utility of results
Genetics in Medicine·2025
When families bridge the research-clinical divide: An exploration of values regarding cascade screening in genomic research
Genetics in Medicine Open·2025Open Access
Patient understanding of prenatal exome sequencing
American Journal of Obstetrics & Gynecology MFM·2024· 1 citedOpen Access
Lessons learned while starting multi-institutional genetics research in diverse populations: A report from the Clinical Sequencing Evidence-Generating Research (CSER) consortium
UNC Libraries·2024Open Access
Genetic ancestry and diagnostic yield of exome sequencing in a diverse population
npj Genomic Medicine·2024· 15 citedOpen Access
Trust in prenatal exome sequencing for expectant families facing unexplained fetal anomalies
Prenatal Diagnosis·2023· 3 citedOpen Access
Conducting clinical genomics research during the COVID-19 pandemic: Lessons learned from the CSER consortium experience
UNC Libraries·2023· 1 citedOpen Access
Author Correction: Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population
npj Genomic Medicine·2023· 1 citedOpen Access
The Parent PrU: A measure to assess personal utility of pediatric genomic results
Genetics in Medicine·2023· 10 citedOpen Access
Access to prenatal exome sequencing for fetal malformations: A qualitative landscape analysis in the US
Prenatal Diagnosis·2023· 5 citedOpen Access
Parent-Reported Clinical Utility of Pediatric Genomic Sequencing
PEDIATRICS·2023· 13 citedOpen Access
Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population
npj Genomic Medicine·2023· 40 citedOpen Access
Diagnostic Yield of Exome Sequencing in a Diverse Pediatric and Prenatal Population is not Associated with Genetic Ancestry
2023Open Access
Patient perspectives on the utility and impact of prenatal exome sequencing
American Journal of Obstetrics and Gynecology·2023
Lessons learned while starting multi-institutional genetics research in diverse populations: A report from the Clinical Sequencing Evidence-Generating Research (CSER) consortium
Contemporary Clinical Trials·2022· 2 citedOpen Access
Conducting clinical genomics research during the <scp>COVID</scp>‐19 pandemic: Lessons learned from the <scp>CSER</scp> consortium experience
American Journal of Medical Genetics Part A·2022· 2 citedOpen Access
Parental Hopes and Understandings of the Value of Prenatal Diagnostic Genomic Sequencing: A Qualitative Analysis
Frontiers in Genetics·2022· 9 citedOpen Access
Perspectives and preferences regarding genomic secondary findings in underrepresented prenatal and pediatric populations: A mixed-methods approach
Genetics in Medicine·2022· 13 citedOpen Access
A Qualitative Study of Obstacles to Diaphragm and Condom Use in an HIV Prevention Trial in Sub-Saharan Africa
AIDS Education and Prevention·2012· 15 cited
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Frequent Co-authors

Sara Ackerman(11), Mary E. Norton(10), Teresa N. Sparks(8), Anne Slavotinek(7), Billie R. Lianoglou(7), Ariane van der Straten(6), Sibongile Mtetwa(5), Simon Outram(5), Jessica Van Ziffle(5), Uğur Hodoğlugil(5), Barbara A. Koenig(5), Lucia A. Hindorff(5), Mark Kvale(4), Yusuph Mavura(4), W. Patrick Devine(4), Pierre‐Marie Martin(4), Neil Risch(4), Pui–Yan Kwok(4), Heidi V. Russell(4), Jeannette T. Bensen(4)