Jill A. Fahrner

Jill A. Fahrner

Pediatrics | Medical Genetics

200 North Wolfe Street, Rubenstein BLDG Lower Level
Rubenstein BLDG Lower Level
Baltimore, MD 21287

Last Updated: 09/26/2026

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Found 37 publications

Androgens mediate sexual dimorphism in Pilarowski-Bjornsson syndrome.

Androgens mediate sexual dimorphism in Pilarowski-Bjornsson syndrome.

Journal: American journal of human genetics

Published: June 05, 2026

Androgens mediate sexual dimorphism in Pilarowski-Bjornsson Syndrome.

Androgens mediate sexual dimorphism in Pilarowski-Bjornsson Syndrome.

Journal: medRxiv : the preprint server for health sciences

Published: May 19, 2025

KMT2D Deficiency Causes Sensorineural Hearing Loss in Mice and Humans.

KMT2D Deficiency Causes Sensorineural Hearing Loss in Mice and Humans.

Journal: Genes

Published: December 05, 2023

Growth deficiency in a mouse model of Kabuki syndrome 2 bears mechanistic similarities to Kabuki syndrome 1.

Growth deficiency in a mouse model of Kabuki syndrome 2 bears mechanistic similarities to Kabuki syndrome 1.

Journal: PLoS genetics

Published: October 16, 2023

Novel mouse model of Weaver syndrome displays overgrowth and excess osteogenesis reversible with KDM6A/6B inhibition.

Novel mouse model of Weaver syndrome displays overgrowth and excess osteogenesis reversible with KDM6A/6B inhibition.

Journal: bioRxiv : the preprint server for biology

Published: July 10, 2023

A mouse model of Weaver syndrome displays overgrowth and excess osteogenesis reversible with KDM6A/6B inhibition.

A mouse model of Weaver syndrome displays overgrowth and excess osteogenesis reversible with KDM6A/6B inhibition.

Journal: JCI insight

Published: June 23, 2023

Associations Between Executive Functioning, Behavioral Functioning, and Adaptive Functioning Difficulties in Wiedemann-Steiner Syndrome.

Associations Between Executive Functioning, Behavioral Functioning, and Adaptive Functioning Difficulties in Wiedemann-Steiner Syndrome.

Journal: Archives of clinical neuropsychology : the official journal of the National Academy of Neuropsychologists

Published: May 01, 2023

Five years of experience in the Epigenetics and Chromatin Clinic: what have we learned and where do we go from here?

Five years of experience in the Epigenetics and Chromatin Clinic: what have we learned and where do we go from here?

Journal: Human genetics

Published: October 15, 2022

The social phenotype associated with Wiedemann-Steiner syndrome: Autistic traits juxtaposed with high social drive and prosociality.

The social phenotype associated with Wiedemann-Steiner syndrome: Autistic traits juxtaposed with high social drive and prosociality.

Journal: American journal of medical genetics. Part A

Published: September 13, 2022

Individuals with Wiedemann-Steiner syndrome show nonverbal reasoning and visuospatial defects with relative verbal skill sparing.

Individuals with Wiedemann-Steiner syndrome show nonverbal reasoning and visuospatial defects with relative verbal skill sparing.

Journal: Journal of the International Neuropsychological Society : JINS

Published: September 05, 2022

Anxiety in Wiedemann-Steiner syndrome.

Anxiety in Wiedemann-Steiner syndrome.

Journal: American journal of medical genetics. Part A

Published: July 12, 2022

Sleep disturbances correlate with behavioral problems among individuals with Wiedemann-Steiner syndrome.

Sleep disturbances correlate with behavioral problems among individuals with Wiedemann-Steiner syndrome.

Journal: Frontiers in genetics

Published: May 22, 2022

Showing 1-12 of 37

Last Updated: 09/26/2026