Jill A. Fahrner, Ph.D.

Affiliations: 
2005 Johns Hopkins University, Baltimore, MD 
Area:
Molecular Biology, Genetics, Oncology
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"Jill Fahrner"

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Stephen B. Baylin grad student 2005 Johns Hopkins
 (Aberrant epigenetic silencing of tumor suppressor genes in human cancer: The roles of DNA hypermethylation and the histone code.)
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Publications

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Harris JR, Gao CW, Britton JF, et al. (2023) Five years of experience in the Epigenetics and Chromatin Clinic: what have we learned and where do we go from here? Human Genetics. 1-18
Levy MA, Relator R, McConkey H, et al. (2022) Functional correlation of genome-wide DNA methylation profiles in genetic neurodevelopmental disorders. Human Mutation
Montano C, Britton JF, Harris JR, et al. (2022) Genome-wide DNA methylation profiling confirms a case of low-level mosaic Kabuki syndrome 1. American Journal of Medical Genetics. Part A
Brennan K, Zheng H, Fahrner JA, et al. (2022) NSD1 mutations deregulate transcription and DNA methylation of bivalent developmental genes in Sotos syndrome. Human Molecular Genetics
Levy MA, McConkey H, Kerkhof J, et al. (2022) Novel diagnostic DNA methylation episignatures expand and refine the epigenetic landscapes of Mendelian disorders. Hgg Advances. 3: 100075
Levy MA, Beck DB, Metcalfe K, et al. (2021) Author Correction: Deficiency of TET3 leads to a genome-wide DNA hypermethylation episignature in human whole blood. Npj Genomic Medicine. 6: 100
Levy MA, Beck DB, Metcalfe K, et al. (2021) Deficiency of TET3 leads to a genome-wide DNA hypermethylation episignature in human whole blood. Npj Genomic Medicine. 6: 92
Beck DB, Petracovici A, He C, et al. (2020) Delineation of a Human Mendelian Disorder of the DNA Demethylation Machinery: TET3 Deficiency. American Journal of Human Genetics
Fahrner JA, Bjornsson HT. (2019) Mendelian disorders of the epigenetic machinery: postnatal malleability and therapeutic prospects. Human Molecular Genetics
Fahrner JA, Bjornsson HT. (2014) Mendelian disorders of the epigenetic machinery: tipping the balance of chromatin states. Annual Review of Genomics and Human Genetics. 15: 269-93
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