Katinka A. Vigh‐Conrad

Author

Washington University in St. Louis ORCID

Also Known As

K. A. Vigh-Conrad, K.A. Vigh‐Conrad, Katinka A Vigh-Conrad, Katinka A. Vigh-Conrad, Katinka A. Vigh‐Conrad, Katinka Vigh-Conrad

Publications

701

Citations

H-Index

Concepts

All Affiliations

Washington University in St. Louis Oregon Health & Science University Oregon National Primate Research Center University of Utah University of California, San Francisco

About

Katinka A. Vigh‐Conrad is an author at Washington University in St. Louis specializing in medicine, molecular diagnostics, and tumor heterogeneity.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	306
2	Health Sciences	2	2	61
3	Engineering	1	1	44
4	Natural Sciences	1	1	30
5	Public Health	1	1	28

Katinka A. Vigh‐Conrad

Publications

608

Citations

H-Index

Page 1

	Year	Citations
Analyzing the Genetic Spectrum of Vascular Anomalies with Overgrowth via Cancer Genomics Dawn H. Siegel, Catherine E. Cottrell, Jenna L. Streicher, Journal of Investigative Dermatology AngiogenesisSomatic VariantTumor HeterogeneityVascular AnomaliesGenetics	2017	74
Diverse monogenic subforms of human spermatogenic failure Liina Nagirnaja, Alexandra M. Lopes, Wu‐Lin Charng, Nature Communications	2022	72
Comparative single-cell analysis of biopsies clarifies pathogenic mechanisms in Klinefelter syndrome Eisa Mahyari, Jingtao Guo, Ana C. Lima, The American Journal of Human Genetics Cell LineageKlinefelter SyndromeComparative Single-cell AnalysisCell DivisionCytogenetics	2021	69
Somatic PIK3R1 variation as a cause of vascular malformations and overgrowth Catherine E. Cottrell, Nicole R. Bender, Michael T. Zimmermann, Genetics in Medicine	2021	58
TAD evolutionary and functional characterization reveals diversity in mammalian TAD boundary properties and function Mariam Okhovat, Jake VanCampen, Kimberly A. Nevonen, Nature Communications	2023	54
Utility of clinical high‐depth next generation sequencing for somatic variant detection in the <i><scp>PIK3CA</scp></i>‐related overgrowth spectrum Vishwanathan Hucthagowder, Archana Shenoy, Meagan Corliss, Clinical Genetics EngineeringGeneticsGenetic EpidemiologyPathologySomatic Variant Detection	2016	44
Rare mutations in the complement regulatory gene CSMD1 are associated with male and female infertility Arthur S. Lee, Jannette Rusch, Ana C. Lima, Nature Communications	2019	39
Beyond sequence variation: assessment of copy number variation in adult glioblastoma through targeted tumor somatic profiling Samantha N. McNulty, Catherine E. Cottrell, Katinka A. Vigh‐Conrad, Human Pathology Neuro-oncologyOncologySomatic VariantGliomaTumor Heterogeneity	2018	31
Organochlorine-mediated potentiation of the general coactivator p300 through p38 mitogen-activated protein kinase Melyssa R. Bratton, Daniel E. Frigo, Katinka A. Vigh‐Conrad, Carcinogenesis Nuclear Transcription FactorsTranscriptional RegulationSignal TransductionSignaling PathwayBiochemistry	2008	30
Targeted Next-Generation Sequencing in Molecular Subtyping of Lower-Grade Diffuse Gliomas Jamal Carter, Samantha N. McNulty, Patrick J. Cimino, Journal of Molecular Diagnostics Neuro-oncologyGliomaTumor HeterogeneityMedicineNext-generation Sequencing	2016	30

Page 1