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Kathleen A. Kaiser‐Rogers

Observed names: K A Kaiser-Rogers, K A Kaiser-rogers, K Kaiser-Rogers, K. Kaiser-Rogers, K.A. Kaiser-Rogers, Kaiser-Rogers, K A, Kaiser-Rogers, Kathleen, Kathleen A Kaiser-Rogers, Kathleen A. Kaiser-Rogers, Kathleen Kaiser-Rogers, Kathleen Kaiser-rogers, Kathleen Kaiser‐Rogers
OpenAlex ID: A5019187002
DNA HELICASES
1990 · Steven W. Matson, Kathleen A. Kaiser-Rogers · Annual Review of Biochemistry · 355
Discordant noninvasive prenatal testing results in a patient subsequently diagnosed with metastatic disease
2013 · C. Michael Osborne, Emily Hardisty, et al. · Prenatal Diagnosis · 231
Androgenetic/biparental mosaicism causes placental mesenchymal dysplasia
2005 · K A Kaiser-Rogers, D E McFadden, et al. · Journal of Medical Genetics · 189
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Increasing the diagnostic yield of exome sequencing by copy number variant analysis
2018 · Daniel S. Marchuk, Kristy Crooks, et al. · PLoS ONE · 89
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Double helicase II (uvrD)-helicase IV (helD) deletion mutants are defective in the recombination pathways of Escherichia coli
1993 · V M Mendonca, K Kaiser-Rogers, et al. · Journal of Bacteriology · 66
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Deletion of Hepatocyte Nuclear Factor-1-Beta in an Infant with Prune Belly Syndrome
2010 · Sina Haeri, Patricia Devers, et al. · American Journal of Perinatology · 56
Aortopathy in the 7q11.23 microduplication syndrome
2014 · Ashley Parrott, Jeanne James, et al. · American Journal of Medical Genetics Part A · 37
PTEN Deficiency Mediates a Reciprocal Response to IGFI and mTOR Inhibition
2014 · Mukund Patel, Nicholas C. Gomez, et al. · Molecular Cancer Research · 36
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Timeless functions independently of the Tim-Tipin complex to promote sister chromatid cohesion in normal human fibroblasts
2011 · Stephanie L. Smith-Roe, Shivani S. Patel, et al. · Cell Cycle · 35
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Lymphomas with pseudo–double-hit BCL6-MYC translocations due to t(3;8)(q27;q24) are associated with a germinal center immunophenotype, extranodal involvement, and frequent BCL2 translocations
2018 · Steven M. Johnson, Jayadev Manikkam Umakanthan, et al. · Human Pathology · 34
Type I diabetes mellitus in a patient with chromosome 22q11.2 deletion syndrome
2001 · Deborah A. Elder, Kathleen Kaiser-Rogers, et al. · American Journal of Medical Genetics · 22
Structural Chromosome Rearrangements
2005 · Kathleen Kaiser-Rogers, Kathleen Rao · Humana Press eBooks · 21
Assignment of the Human Type I IMP Dehydrogenase Gene (IMPDH1) to Chromosome 7q31.3-q32
1994 · Jing Jin Gu, Kathleen Kaiser-Rogers, et al. · Genomics · 19
A Rational Approach to Genetic Testing for Sarcoma
2009 · Margaret L. Gulley, Kathleen A. Kaiser-Rogers · Diagnostic Molecular Pathology · 18
Review: significance of, and optimal screening for, HER-2 gene amplification and protein overexpression in breast carcinoma.
2001 · W K Funkhouser, K Kaiser-Rogers · PubMed · 17
Karyotypic abnormalities associated with Epstein–Barr virus status in classical Hodgkin lymphoma
2016 · Nathan D. Montgomery, Wilborn B. Coward, et al. · Cancer Genetics · 16
Neuroblastoma in a pediatric patient with a microduplication of 2p involving the MYCN locus
2013 · David Van Mater, Erik H. Knelson, et al. · American Journal of Medical Genetics Part A · 15
Submicroscopic deletion 9(q34.4) and duplication 19(p13.3): Identified by subtelomere specific FISH probes
2003 · Denise I. Quigley, Kathleen Kaiser‐Rogers, et al. · American Journal of Medical Genetics Part A · 12
Two cases of acute myeloid leukemia with t(11;17) associated with varying morphology and immunophenotype: rearrangement of the MLL gene and a region proximal to the RARα gene
2005 · Loveleen C. Kang, Scott V. Smith, et al. · Cancer Genetics and Cytogenetics · 11
Usefulness and limitations of FISH to characterize partially cryptic complex chromosome rearrangements
2000 · Kathleen A. Kaiser-Rogers, Kathleen W. Rao, et al. · American Journal of Medical Genetics · 9
Conventional Cytogenetic Analysis of Hematologic Neoplasms: A 20-Year Review of Proficiency Test Results From the College of American Pathologists/American College of Medical Genetics and Genomics Cytogenetics Committee
2020 · Daniel P. Larson, Yassmine M. Akkari, et al. · Archives of Pathology & Laboratory Medicine · 8
Stroke-Like Presentation Following Febrile Seizure in a Patient with 1q43q44 Deletion Syndrome
2016 · J. Elliott Robinson, Stephanie M. Wolfe, et al. · Frontiers in Neurology · 8
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Primary mediastinal B-cell lymphoma: detection of BCL2 gene rearrangements by PCR analysis and FISH
2008 · Cherie H. Dunphy, Dennis P. O’Malley, et al. · Journal of Hematopathology · 7
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Structural Chromosome Rearrangements
1999 · Kathleen Kaiser-Rogers, Kathleen Rao · Humana Press eBooks · 7
Cell‐free DNA testing in a trisomy 21 pregnancy with confined placental mosaicism for a cell line with trisomy for both chromosomes 18 and 21
2015 · Kristy Crooks, Ginger Edwardsen, et al. · Clinical Case Reports · 5
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Works count: 52
Citation count: 1,344
H-index: 16
I10-index: 19
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