Terrence Blaine Crowley

24PUBLICATIONS
152CO-AUTHORS
Developmental genetics (incl. sex determination)Molecular targetsGene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)Gene mapping
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Publications (24)

|Mar 27, 2026
Deletion size and background genetic variation shape congenital heart disease phenotypes in 3,016 individuals with 22q11.2 deletion syndrome.

Jhih-Rong Lin, Daniella Miller, Dana Luong

|Jan 28, 2026
22q11.2 Deletion Syndrome in Offspring Conceived via Assisted Reproductive Technology Versus Spontaneously.

Jennifer Borowka, Terrence Blaine Crowley, Ashika Mani

|Dec 08, 2025
Prevalence and Spectrum of Congenital Heart Disease in Individuals With Distal Chromosome 22q11.22-23 Deletions.

Tanner J Nelson, Daniel E McGinn, T Blaine Crowley

|Jun 16, 2025
ZNF280A links DNA double-strand break repair to human 22q11.2 distal deletion syndrome.

Thomas L Clarke, Hyo Min Cho, Ilaria Ceppi

|Jul 27, 2024
Expanding Genetic Counselor Roles: A Model for Global Research Development.

Colleen C Muraresku, Elizabeth M McCormick, Lydia Rockart

|Jul 24, 2024
Neurocognitive profiles of 22q11.2 and 16p11.2 deletions and duplications.

Ruben C Gur, Carrie E Bearden, Sebastien Jacquemont

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