Tracie Pennimpede

Berlin, BE, Germany

Last Updated: 09/26/2026

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Found 14 publications

First genome-wide association study of esophageal atresia identifies three genetic risk loci at CTNNA3, FOXF1/FOXC2/FOXL1, and HNF1B.

First genome-wide association study of esophageal atresia identifies three genetic risk loci at CTNNA3, FOXF1/FOXC2/FOXL1, and HNF1B.

Journal: HGG advances

Published: October 25, 2021

Intraocular calcidiol: Uncovering a role for vitamin D in the eye.

Intraocular calcidiol: Uncovering a role for vitamin D in the eye.

Journal: The Journal of steroid biochemistry and molecular biology

Published: June 19, 2019

BRACHYURY directs histone acetylation to target loci during mesoderm development.

BRACHYURY directs histone acetylation to target loci during mesoderm development.

Journal: EMBO reports

Published: March 09, 2017

Targeted Resequencing of 29 Candidate Genes and Mouse Expression Studies Implicate ZIC3 and FOXF1 in Human VATER/VACTERL Association.

Targeted Resequencing of 29 Candidate Genes and Mouse Expression Studies Implicate ZIC3 and FOXF1 in Human VATER/VACTERL Association.

Journal: Human mutation

Published: April 27, 2015

Mutations of the SLIT2-ROBO2 pathway genes SLIT2 and SRGAP1 confer risk for congenital anomalies of the kidney and urinary tract.

Mutations of the SLIT2-ROBO2 pathway genes SLIT2 and SRGAP1 confer risk for congenital anomalies of the kidney and urinary tract.

Journal: Human genetics

Published: February 20, 2015

Analysis of the Fam181 gene family during mouse development reveals distinct strain-specific expression patterns, suggesting a role in nervous system development and function.

Analysis of the Fam181 gene family during mouse development reveals distinct strain-specific expression patterns, suggesting a role in nervous system development and function.

Journal: Gene

Published: February 02, 2015

Genome-wide association study and meta-analysis identify ISL1 as genome-wide significant susceptibility gene for bladder exstrophy.

Genome-wide association study and meta-analysis identify ISL1 as genome-wide significant susceptibility gene for bladder exstrophy.

Journal: PLoS genetics

Published: August 20, 2014

Genome-wide association study and mouse expression data identify a highly conserved 32 kb intergenic region between WNT3 and WNT9b as possible susceptibility locus for isolated classic exstrophy of the bladder.

Genome-wide association study and mouse expression data identify a highly conserved 32 kb intergenic region between WNT3 and WNT9b as possible susceptibility locus for isolated classic exstrophy of the bladder.

Journal: Human molecular genetics

Published: May 24, 2014

Classic bladder exstrophy: Frequent 22q11.21 duplications and definition of a 414 kb phenocritical region.

Classic bladder exstrophy: Frequent 22q11.21 duplications and definition of a 414 kb phenocritical region.

Journal: Birth defects research. Part A, Clinical and molecular teratology

Published: February 26, 2014

Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association.

Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association.

Journal: Kidney international

Published: June 05, 2013

De novo microduplications at 1q41, 2q37.3, and 8q24.3 in patients with VATER/VACTERL association.

De novo microduplications at 1q41, 2q37.3, and 8q24.3 in patients with VATER/VACTERL association.

Journal: European journal of human genetics : EJHG

Published: October 30, 2012

Isolated bladder exstrophy associated with a de novo 0.9 Mb microduplication on chromosome 19p13.12.

Isolated bladder exstrophy associated with a de novo 0.9 Mb microduplication on chromosome 19p13.12.

Journal: Birth defects research. Part A, Clinical and molecular teratology

Published: October 13, 2012

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Last Updated: 09/26/2026