Jill A Fahrner

ORCID

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 15

Top Venues

This page only lists publications with an associated author ORCID identifier.

Publications

Christine W Gao, WanYing Lin, Ryan C Riddle, Sheetal Chopra, Jiyoung Kim, Leandros Boukas, Kaspar D Hansen, Hans T Björnsson, Jill A Fahrner
Growth deficiency in a mouse model of Kabuki syndrome 2 bears mechanistic similarities to Kabuki syndrome 1. PLoS genetics 20 (6) (2024)
Christine W Gao, WanYing Lin, Ryan C Riddle, Sheetal Chopra, Jiyoung Kim, Leandros Boukas, Kaspar D Hansen, Hans T Björnsson, Jill A Fahrner
Growth deficiency in a mouse model of Kabuki syndrome 2 bears mechanistic similarities to Kabuki syndrome 1. PLoS genetics 20 (6) (2024)
Christine W Gao, WanYing Lin, Ryan C Riddle, Sheetal Chopra, Jiyoung Kim, Leandros Boukas, Kaspar D Hansen, Hans T Björnsson, Jill A Fahrner
Growth deficiency in a mouse model of Kabuki syndrome 2 bears mechanistic similarities to Kabuki syndrome 1. PLoS genetics 20 (6) (2024)
Allison J Kalinousky, Teresa R Luperchio, Katrina M Schrode, Jacqueline R Harris, Li Zhang, Valerie B DeLeon, Jill A Fahrner, Amanda M Lauer, Hans T Bjornsson
KMT2D Deficiency Causes Sensorineural Hearing Loss in Mice and Humans. Genes 15 (1) (2023)
Allison J Kalinousky, Teresa R Luperchio, Katrina M Schrode, Jacqueline R Harris, Li Zhang, Valerie B DeLeon, Jill A Fahrner, Amanda M Lauer, Hans T Bjornsson
KMT2D Deficiency Causes Sensorineural Hearing Loss in Mice and Humans. Genes 15 (1) (2023)
Jacqueline R Harris, Christine W Gao, Jacquelyn F Britton, Carolyn D Applegate, Hans T Bjornsson, Jill A Fahrner
Five years of experience in the Epigenetics and Chromatin Clinic: what have we learned and where do we go from here? Human genetics (2023)
Jacqueline R Harris, Christine W Gao, Jacquelyn F Britton, Carolyn D Applegate, Hans T Bjornsson, Jill A Fahrner
Five years of experience in the Epigenetics and Chromatin Clinic: what have we learned and where do we go from here? Human genetics (2023)
Allison J Kalinousky, Teresa R Luperchio, Katrina M Schrode, Jacqueline R Harris, Li Zhang, Valerie B DeLeon, Jill A Fahrner, Amanda M Lauer, Hans T Bjornsson
KMT2D Deficiency Causes Sensorineural Hearing Loss in Mice and Humans. Genes 15 (1) (2023)
Allison J Kalinousky, Teresa R Luperchio, Katrina M Schrode, Jacqueline R Harris, Li Zhang, Valerie B DeLeon, Jill A Fahrner, Amanda M Lauer, Hans T Bjornsson
KMT2D Deficiency Causes Sensorineural Hearing Loss in Mice and Humans. Genes 15 (1) (2023)
Allison J Kalinousky, Teresa R Luperchio, Katrina M Schrode, Jacqueline R Harris, Li Zhang, Valerie B DeLeon, Jill A Fahrner, Amanda M Lauer, Hans T Bjornsson
KMT2D Deficiency Causes Sensorineural Hearing Loss in Mice and Humans. Genes 15 (1) (2023)
Allison J Kalinousky, Teresa R Luperchio, Katrina M Schrode, Jacqueline R Harris, Li Zhang, Valerie B DeLeon, Jill A Fahrner, Amanda M Lauer, Hans T Bjornsson
KMT2D Deficiency Causes Sensorineural Hearing Loss in Mice and Humans. Genes 15 (1) (2023)
Christine W Gao, WanYing Lin, Ryan C Riddle, Priyanka Kushwaha, Leandros Boukas, Hans Tomas Bjornsson, Kaspar D Hansen, Jill A Fahrner
Novel mouse model of Weaver syndrome displays overgrowth and excess osteogenesis reversible with KDM6A/6B inhibition. bioRxiv : the preprint server for biology (2023)
Carolina Montano, Jacquelyn F Britton, Jacqueline R Harris, Jennifer Kerkhof, Benjamin T Barnes, Jennifer A Lee, Bekim Sadikovic, Nara Lygia de Macena Sobreira, Jill A Fahrner
Genome-wide DNA methylation profiling confirms a case of low-level mosaic Kabuki syndrome 1. American journal of medical genetics. Part A 188 (7) (2022)
Michael A Levy, David B Beck, Kay Metcalfe, Sofia Douzgou Houge, Sivagamy Sithambaram, Trudie Cottrell, Muhammad Ansar, Jennifer Kerkhof, Cyril Mignot, Marie-Christine Nougues, Boris Keren, Hannah W Moore, Renske Oegema, Jacques C Giltay, Marleen Simon, Richard H van Jaarsveld, Jessica Bos, Mieke van Haelst, M Mahdi Motazacker, Elles M J Boon, Gijs W E Santen, Claudia A L Ruivenkamp, Marielle Alders, Teresa Romeo Luperchio, Leandros Boukas, Keri Ramsey, Vinodh Narayanan, G Bradley Schaefer, Roberto Bonasio, Kimberly F Doheny, Roger E Stevenson, Siddharth Banka, Bekim Sadikovic, Jill A Fahrner
Deficiency of TET3 leads to a genome-wide DNA hypermethylation episignature in human whole blood. NPJ genomic medicine 6 (1) (2021)
Michael A Levy, David B Beck, Kay Metcalfe, Sofia Douzgou Houge, Sivagamy Sithambaram, Trudie Cottrell, Muhammad Ansar, Jennifer Kerkhof, Cyril Mignot, Marie-Christine Nougues, Boris Keren, Hannah W Moore, Renske Oegema, Jacques C Giltay, Marleen Simon, Richard H van Jaarsveld, Jessica Bos, Mieke van Haelst, M Mahdi Motazacker, Elles M J Boon, Gijs W E Santen, Claudia A L Ruivenkamp, Marielle Alders, Teresa Romeo Luperchio, Leandros Boukas, Keri Ramsey, Vinodh Narayanan, G Bradley Schaefer, Roberto Bonasio, Kimberly F Doheny, Roger E Stevenson, Siddharth Banka, Bekim Sadikovic, Jill A Fahrner
Author Correction: Deficiency of TET3 leads to a genome-wide DNA hypermethylation episignature in human whole blood. NPJ genomic medicine 6 (1) (2021)

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Publication Activity (10 Years)

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Jill A Fahrner