Steve Seltzsam

Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations

Dervla M. Connaughton, Rufeng Dai, Danielle Owen et al. · The American Journal of Human Genetics · 2020 · 49 citations · Full text

Medicine, Genetics, Developmental Biology +1

Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUT

Steve Seltzsam, Chunyan Wang, Bixia Zheng et al. · Genetics in Medicine · 2021 · 36 citations · Full text

Allelic Variant, Genetic Disorder, Exome Sequencing +7

DAAM2 Variants Cause Nephrotic Syndrome via Actin Dysregulation

Ronen Schneider, Konstantin Deutsch, Gregory J. Hoeprich et al. · The American Journal of Human Genetics · 2020 · 30 citations · Full text

Glomerulonephritis, Autoimmune Disease, Medicine +7

Phenotype expansion of heterozygous FOXC1 pathogenic variants toward involvement of congenital anomalies of the kidneys and urinary tract (CAKUT)

Chen‐Han Wilfred Wu, Nina Mann, Makiko Nakayama et al. · Genetics in Medicine · 2020 · 22 citations · Full text

Urological Research, Urology, Phenotype Expansion +9

Roscovitine strongly enhances the effect of olaparib on radiosensitivity for HPV neg. but not for HPV pos. HNSCC cell lines

Frank Ziemann, Steve Seltzsam, Kristin Dreffke et al. · Oncotarget · 2017 · 21 citations · Full text