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Lynne S. Rosenblum

Prenatal diagnosis of Fanconi anemia (Group C) subsequent to abnormal sonographic findings
2005 · Amy Merrill, Lynne Rosenblum-Vos, et al. · Prenatal Diagnosis · 87
Transmission of a T-Cell Lymphoma by Allogeneic Bone Marrow Transplantation
2001 · Karin D. Berg, Nooshin K. Brinster, et al. · New England Journal of Medicine · 84
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Cystic Fibrosis Carrier Testing in an Ethnically Diverse US Population
2011 · Elizabeth M Rohlfs, Zhaoqing Zhou, et al. · Clinical Chemistry · 76
Structure and Organization of Amplified DNA on Double Minutes Containing the mdm2 Oncogene
1993 · Steven S. Fakharzadeh, Lynne Rosenblum-Vos, et al. · Genomics · 66
A yeast protein with homology to the β-subunit of G proteins is involved in control of heme-regulated and catabolite-repressed genes
1991 · Ming Zhang, Lynne S. Rosenblum-Vos, et al. · Gene · 65
Mosaic trisomy 16 ascertained through amniocentesis: Evaluation of 11 new cases
1998 · Wei-Tong Hsu, Dmitriy A. Shchepin, et al. · American Journal of Medical Genetics · 42
Complex chromosomal rearrangements: some breakpoints may have cellular adaptive significance
1994 · Iosif W. Lurie, Eric A. Wulfsberg, et al. · Clinical Genetics · 23
Comparative assessment of gene-specific variant distribution in prenatal and postnatal cohorts tested for Noonan syndrome and related conditions
2018 · N.T. Leach, D.R. Wilson Mathews, et al. · Genetics in Medicine · 21
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A human-murine chimera model for in utero human hematopoietic stem cell transplantation
1999 · Wing Leung, Karin Blakemore, et al. · Transplantation and Cellular Therapy · 19
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Cytogenetic studies of primary cultures of esophageal squamous cell carcinoma
1993 · Lynne S. Rosenblum-Vos, Stephen J. Meltzer, et al. · Cancer Genetics and Cytogenetics · 18
The Emergence of Artificial Intelligence-Guided Karyotyping: A Review and Reflection
2025 · Lynne S. Rosenblum, Julia Holmes, et al. · Genes · 16
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Incidental molecular diagnoses and heterozygous risk alleles in a carrier screening cohort
2022 · Jennifer Reiner, Lynne S. Rosenblum, et al. · Genetics in Medicine · 15
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Correction: Comparative assessment of gene-specific variant distribution in prenatal and postnatal cohorts tested for Noonan syndrome and related conditions
2018 · N.T. Leach, D.R. Wilson Mathews, et al. · Genetics in Medicine · 13
Response to genetic counseling and testing for the APC I1307K mutation
2000 · Karen A. Johnson, Lynne Rosenblum-Vos, et al. · American Journal of Medical Genetics · 13
Variant Classification for Pompe disease; ACMG/AMP specifications from the ClinGen Lysosomal Diseases Variant Curation Expert Panel
2023 · Jennifer L. Goldstein, Jennifer McGlaughon, et al. · Molecular Genetics and Metabolism · 12
The ROX3 Gene Encodes an Essential Nuclear Protein Involved in CYC7 Gene Expression in Saccharomyces cerevisiae
1991 · Lynne S. Rosenblum-Vos, Linda Rhodes, et al. · Molecular and Cellular Biology · 12
Comparison of pan‐ethnic and ethnic‐based carrier screening panels for individuals of Ashkenazi Jewish descent
2019 · Lynne S. Rosenblum, Hui Zhu, et al. · Journal of Genetic Counseling · 7
Prenatal Testing for Variants in Genes Associated with Hereditary Cancer Risk
2024 · Lynne S. Rosenblum, Stephanie M. Auger, et al. · Journal of Molecular Diagnostics · 4
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A customized scaffolds approach for the detection and phasing of complex variants by next-generation sequencing
2020 · Qiandong Zeng, Natalia T. Leach, et al. · Scientific Reports · 4
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An immunohistochemical germinal center B-cell dark zone signature identifies Burkitt lymphoma and molecular high-grade B-cell lymphomas
2025 · Xiaoxian Zhao, Alexandra Balmaceda, et al. · American Journal of Clinical Pathology · 3
1: Multicenter evaluation of a new AI-based karyotyping software on bone marrow specimens
2025 · Rachel D. Burnside, Julie Best, et al. · Genetics in Medicine Open · 3
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P684: Improved karyotyping efficiency with artificial intelligence: A multicenter evaluation of peripheral blood karyogram
2025 · Rachel Burnside, Katy Phelan, et al. · Genetics in Medicine Open · 3
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P671: New artificial intelligence-based computer-aided chromosome analysis and karyotyping: A pilot evaluation
2024 · Agshin Taghiyev, Julie Best, et al. · Genetics in Medicine Open · 2
P600: Multicenter pilot evaluation of a new AI-based metaphase finder for application in karyotyping peripheral blood and bone marrow specimens
2026 · Lynne S. Rosenblum, Katy Phelan, et al. · Genetics in Medicine Open · 1
P100: BCR/ABL1 p230 transcript in B-lymphoblastic leukemia/lymphoma: A case report
2024 · Agshin Taghiyev, Christopher Giauque, et al. · Genetics in Medicine Open · 1
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Works count: 29
Citation count: 611
H-index: 13
I10-index: 16
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