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Author Details
Full Name
Katinka A Vigh-Conrad
Affiliation
ORCID
Career Start Year
2005
Papers
19
H Index
11
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37053313
The origins and functional effects of postzygotic mutations throughout the human life span.
Science
2023
38062027
TAD evolutionary and functional characterization reveals diversity in mammalian TAD boundary properties and function.
Nat Commun
2023
37267208
Consensus label propagation with graph convolutional networks for single-cell RNA sequencing cell type annotation.
2023
36945527
TAD Evolutionary and functional characterization reveals diversity in mammalian TAD boundary properties and function.
bioRxiv
2023
36572685
Diverse monogenic subforms of human spermatogenic failure.
2022
36214638
SATINN: an automated neural network-based classification of testicular sections allows for high-throughput histopathology of mouse mutants.
2022
34626582
Comparative single-cell analysis of biopsies clarifies pathogenic mechanisms in Klinefelter syndrome.
American Journal of Human Genetics
2021
34040190
Somatic PIK3R1 variation as a cause of vascular malformations and overgrowth.
Genet Med
2021
30594748
Beyond sequence variation: assessment of copy number variation in adult glioblastoma through targeted tumor somatic profiling.
Hum Pathol
2019
31604923
Rare mutations in the complement regulatory gene CSMD1 are associated with male and female infertility.
Nat Commun
2019
29174369
Analyzing the Genetic Spectrum of Vascular Anomalies with Overgrowth via Cancer Genomics.
J Invest Dermatol
2018
28042970
Targeted Next-Generation Sequencing in Molecular Subtyping of Lower-Grade Diffuse Gliomas: Application of the World Health Organization's 2016 Revised Criteria for Central Nervous System Tumors.
J Mol Diagn
2017
28752844
Routine use of clinical exome-based next-generation sequencing for evaluation of patients with thrombotic microangiopathies.
Mod Pathol
2017
28835367
<i>FGFR2</i> amplification in colorectal adenocarcinoma.
Cold Spring Harb Mol Case Stud
2017
28658705
How to Map the Genetic Basis for Conditions that are Comorbid with Male Infertility.
Seminars in Reproductive Medicine
2017
27307077
Utility of clinical high-depth next generation sequencing for somatic variant detection in the PIK3CA-related overgrowth spectrum.
Clin Genet
2017
20419087
A protein allergen microarray detects specific IgE to pollen surface, cytoplasmic, and commercial allergen extracts.
PLoS ONE
2010
18791200
Organochlorine-mediated potentiation of the general coactivator p300 through p38 mitogen-activated protein kinase.
Carcinogenesis
2009
15603917
Xenobiotic-induced TNF-alpha expression and apoptosis through the p38 MAPK signaling pathway.
Toxicology Letters
2005
1 - 19 of 19
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