Publications by authors named "Holly Welsh"

Claim this Profile
I
Insurance denials and diagnostic rates in a pediatric genomic research cohort.
Tricia N Zion, Courtney D Berrios, Ana S A Cohen, Lauren Bartik, Laura A Cross, Holly Welsh

Genet Med· May 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Phenotypic expansion and variable expressivity in individuals with JARID2-related intellectual disability: A case series.
Maxime Cadieux-Dion, Emily Farrow, Isabelle Thiffault, Ana S A Cohen, Holly Welsh

Clin Genet· August 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genomic answers for children: Dynamic analyses of >1000 pediatric rare disease genomes.
Ana S A Cohen, Emily G Farrow, Ahmed T Abdelmoity, Joseph T Alaimo, Shivarajan M Amudhavalli, Holly Welsh

Genet Med· June 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mindfulness-based interventions for cancer-related pain and depression: a narrative review of current evidence and future potential.
Jennie Baxter, Holly Welsh, Justin Grayer

Curr Opin Support Palliat Care· June 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Novel mosaic SRY gene deletions in three newborn males with variable genitourinary malformations.
Jennifer Roberts, Dmitry Lyalin, Norwood Tosatto, Pratibha Rana, Hiba Fadoul, Holly Welsh

Am J Med Genet A· September 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
Hypotonia and intellectual disability without dysmorphic features in a patient with PIGN-related disease.
Isabelle Thiffault, Britton Zuccarelli, Holly Welsh, Xuan Yuan, Emily Farrow

BMC Med Genet· November 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A patient with polymerase E1 deficiency (POLE1): clinical features and overlap with DNA breakage/instability syndromes.
Isabelle Thiffault, Carol Saunders, Janda Jenkins, Nikita Raje, Kristi Canty, Holly I Welsh

BMC Med Genet· May 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Family history and clefting as major criteria for CHARGE syndrome.
Susan Starling Hughes, Holly I Welsh, Nicole P Safina, Khemissa Bejaoui, Holly H Ardinger

Am J Med Genet A· January 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
CDKN1C mutations and genital anomalies.
Holly I Welsh, Tracy L Stockley, Nicole Parkinson, Holly H Ardinger

Am J Med Genet A· January 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis