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Priyanka Murali · SciRah

Researcher profile · Semantic Scholar

Priyanka Murali

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Priyanka Murali — researcher profile on SciRah

h-index: 5
Works: 13
Citations: 226

Most-cited papers

Returning integrated genomic risk and clinical recommendations: the eMERGE study
Jodell E. Linder, Aimee Allworth, Harris T. Bland, P. Caraballo +102 more
2023Genetics in Medicine106 citations Open access
Semantic Scholar
Variant Classification Concordance using the ACMG-AMP Variant Interpretation Guidelines across Nine Genomic Implementation Research Studies.
L. Amendola, Kathleen Muenzen, L. Biesecker, K. Bowling +26 more
2020American Journal of Human Genetics81 citations Open access
Semantic Scholar
Cost-effectiveness frameworks for comparing genome and exome sequencing versus conventional diagnostic pathways: A scoping review and recommended methods
B. Ferket, Z. Baldwin, Priyanka Murali, Akila Pai +11 more
2022Genetics in Medicine13 citations Open access
Semantic Scholar
Two patients with FOXF1 mutations with alveolar capillary dysplasia with misalignment of pulmonary veins and other malformations: Two different presentations and outcomes
A. Abu-El-Haija, Jeffery R. Fineman, Andrew J. Connolly, Priyanka Murali +2 more
2018American Journal of Medical Genetics. Part A12 citations
Semantic Scholar
Lessons learned and recommendations for data coordination in collaborative research: The CSER consortium experience
Kathleen Muenzen, L. Amendola, Tia L. Kauffman, Kathleen F. Mittendorf +16 more
2022HGG advances9 citations Open access
Semantic Scholar
Lessons Learned While Starting Multi-Institutional Genetics Research in Diverse Populations: A Report from the Clinical Sequencing Evidence-Generating Research (CSER) Consortium
H. Russell, H. Smith, J. Bensen, Priyanka Murali +4 more
2022Contemporary Clinical Trials3 citations Open access
Semantic Scholar
Expanding implementation of pediatric whole-genome sequencing: Insights from SeqFirst providers to inform equitable access to a precise genetic diagnosis
Joon-Ho Yu, Katherine E. MacDuffie, Olivia M. Sommerland, Tesla N. Theoryn +17 more
2025HGG advances2 citations
Semantic Scholar
Information-Seeking Preferences in Diverse Patients Receiving a Genetic Testing Result in the Clinical Sequencing Evidence-Generating Research (CSER) Study
A. Slavotinek, Hannah Prasad, S. Outram, S. Scollon +11 more
2023Genetics in Medicine1 citations Open access
Semantic Scholar
Fourth Annual Summer Research Summit on Health Equity Organized by the Center of Excellence in Health Equity, Training and Research, Baylor College of Medicine, Houston, Texas 77030, USA on May 20, 2021
A. Naik, A. Rajagopal, Adam R. Floyd, A. Gil +235 more
2021International Journal of MCH and AIDS1 citations Open access
Semantic Scholar
Capturing Perceived Utility from Qualitative Studies of Genomic Sequencing: Translating a Conceptual Model into a Working Codebook
Betty Cohn, Tesla N. Theoryn, Olivia M. Sommerland, Priyanka Murali +7 more
2026AJOB Empirical Bioethics0 citations
Semantic Scholar
Parent/caregiver needs during pediatric genome‐wide sequencing: A scoping literature review
Priyanka Murali, Joon-Ho Yu
2025medRxiv0 citations Open access
Semantic Scholar
P591: Parental needs during pediatric whole genome sequencing for developmental disorders: An interview study
Priyanka Murali, Joon-Ho Yu, Katherine E. MacDuffie, Michael Bamshad +6 more
2025Genetics in Medicine Open0 citations Open access
Semantic Scholar
eP516: Cost-effectiveness frameworks for comparing genome and exome sequencing versus conventional diagnostic pathways
B. Ferket, Z. Baldwin, Priyanka Murali, Akila Pai +8 more
2022Genetics in Medicine0 citations Open access
Semantic Scholar

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