Vigh-Conrad KA - Search Results

1

TAD evolutionary and functional characterization reveals diversity in mammalian TAD boundary properties and function.

Okhovat M, VanCampen J, Nevonen KA, Harshman L, Li W, Layman CE, Ward S, Herrera J, Wells J, Sheng RR, Mao Y, Ndjamen B, Lima AC, Vigh-Conrad KA, Stendahl AM, Yang R, Fedorov L, Matthews IR, Easow SA, Chan DK, Jan TA, Eichler EE, Rugonyi S, Conrad DF, Ahituv N, Carbone L. Okhovat M, et al. Among authors: vigh conrad ka. Nat Commun. 2023 Dec 7;14(1):8111. doi: 10.1038/s41467-023-43841-8. Nat Commun. 2023. PMID: 38062027 Free PMC article.

2

Utility of clinical high-depth next generation sequencing for somatic variant detection in the PIK3CA-related overgrowth spectrum.

Hucthagowder V, Shenoy A, Corliss M, Vigh-Conrad KA, Storer C, Grange DK, Cottrell CE. Hucthagowder V, et al. Clin Genet. 2017 Jan;91(1):79-85. doi: 10.1111/cge.12819. Epub 2016 Jul 26. Clin Genet. 2017. PMID: 27307077

3

FGFR2 amplification in colorectal adenocarcinoma.

Carter JH, Cottrell CE, McNulty SN, Vigh-Conrad KA, Lamp S, Heusel JW, Duncavage EJ. Carter JH, et al. Cold Spring Harb Mol Case Stud. 2017 Nov 21;3(6):a001495. doi: 10.1101/mcs.a001495. Print 2017 Nov. Cold Spring Harb Mol Case Stud. 2017. PMID: 28835367 Free PMC article.

4

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.

Carter JH, McNulty SN, Cimino PJ, Cottrell CE, Heusel JW, Vigh-Conrad KA, Duncavage EJ. Carter JH, et al. J Mol Diagn. 2017 Mar;19(2):328-337. doi: 10.1016/j.jmoldx.2016.10.010. Epub 2016 Dec 30. J Mol Diagn. 2017. PMID: 28042970 Free article.

5

Routine use of clinical exome-based next-generation sequencing for evaluation of patients with thrombotic microangiopathies.

Gaut JP, Jain S, Pfeifer JD, Vigh-Conrad KA, Corliss M, Sharma MK, Heusel JW, Cottrell CE. Gaut JP, et al. Mod Pathol. 2017 Dec;30(12):1739-1747. doi: 10.1038/modpathol.2017.90. Epub 2017 Jul 28. Mod Pathol. 2017. PMID: 28752844 Free PMC article.

6

A protein allergen microarray detects specific IgE to pollen surface, cytoplasmic, and commercial allergen extracts.

Vigh-Conrad KA, Conrad DF, Preuss D. Vigh-Conrad KA, et al. PLoS One. 2010 Apr 16;5(4):e10174. doi: 10.1371/journal.pone.0010174. PLoS One. 2010. PMID: 20419087 Free PMC article.

7

How to Map the Genetic Basis for Conditions that are Comorbid with Male Infertility.

Nagirnaja L, Vigh-Conrad K, Conrad DF. Nagirnaja L, et al. Semin Reprod Med. 2017 May;35(3):225-230. doi: 10.1055/s-0037-1603567. Epub 2017 Jun 28. Semin Reprod Med. 2017. PMID: 28658705 Review. No abstract available.

8

Rare mutations in the complement regulatory gene CSMD1 are associated with male and female infertility.

Lee AS, Rusch J, Lima AC, Usmani A, Huang N, Lepamets M, Vigh-Conrad KA, Worthington RE, Mägi R, Wu X, Aston KI, Atkinson JP, Carrell DT, Hess RA, O'Bryan MK, Conrad DF. Lee AS, et al. Among authors: vigh conrad ka. Nat Commun. 2019 Oct 11;10(1):4626. doi: 10.1038/s41467-019-12522-w. Nat Commun. 2019. PMID: 31604923 Free PMC article.

9

Comparative single-cell analysis of biopsies clarifies pathogenic mechanisms in Klinefelter syndrome.

Mahyari E, Guo J, Lima AC, Lewinsohn DP, Stendahl AM, Vigh-Conrad KA, Nie X, Nagirnaja L, Rockweiler NB, Carrell DT, Hotaling JM, Aston KI, Conrad DF. Mahyari E, et al. Among authors: vigh conrad ka. Am J Hum Genet. 2021 Oct 7;108(10):1924-1945. doi: 10.1016/j.ajhg.2021.09.001. Am J Hum Genet. 2021. PMID: 34626582 Free PMC article.

10

SATINN: an automated neural network-based classification of testicular sections allows for high-throughput histopathology of mouse mutants.

Yang R, Stendahl AM, Vigh-Conrad KA, Held M, Lima AC, Conrad DF. Yang R, et al. Among authors: vigh conrad ka. Bioinformatics. 2022 Nov 30;38(23):5288-5298. doi: 10.1093/bioinformatics/btac673. Bioinformatics. 2022. PMID: 36214638 Free PMC article.

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