Alexander M. Zink

Wuppertal, NW, Germany

Last Updated: 09/26/2026

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Found 21 publications

Expression quantitative trait loci influence DNA damage-induced apoptosis in cancer.

Expression quantitative trait loci influence DNA damage-induced apoptosis in cancer.

Journal: BMC genomics

Published: August 05, 2024

Investigation into the Health Effects of Reduced Chymase Function Using Predicted Loss-of-Function Mutations in CMA1.

Investigation into the Health Effects of Reduced Chymase Function Using Predicted Loss-of-Function Mutations in CMA1.

Journal: Journal of cardiovascular translational research

Published: February 08, 2022

Protein expression profiling suggests relevance of noncanonical pathways in isolated pulmonary embolism.

Protein expression profiling suggests relevance of noncanonical pathways in isolated pulmonary embolism.

Journal: Blood

Published: December 17, 2019

Nine newly identified individuals refine the phenotype associated with MYT1L mutations.

Nine newly identified individuals refine the phenotype associated with MYT1L mutations.

Journal: American journal of medical genetics. Part A

Published: November 07, 2019

Candidate Genes for Nonsyndromic Cleft Palate Detected by Exome Sequencing.

Candidate Genes for Nonsyndromic Cleft Palate Detected by Exome Sequencing.

Journal: Journal of dental research

Published: August 03, 2017

Further evidence for deletions in 7p14.1 contributing to nonsyndromic cleft lip with or without cleft palate.

Further evidence for deletions in 7p14.1 contributing to nonsyndromic cleft lip with or without cleft palate.

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

Published: July 08, 2016

De novo nonsense and frameshift variants of TCF20 in individuals with intellectual disability and postnatal overgrowth.

De novo nonsense and frameshift variants of TCF20 in individuals with intellectual disability and postnatal overgrowth.

Journal: European journal of human genetics : EJHG

Published: October 26, 2015

De novo microdeletions and point mutations affecting SOX2 in three individuals with intellectual disability but without major eye malformations.

De novo microdeletions and point mutations affecting SOX2 in three individuals with intellectual disability but without major eye malformations.

Journal: American journal of medical genetics. Part A

Published: October 07, 2015

Haploinsufficiency of MeCP2-interacting transcriptional co-repressor SIN3A causes mild intellectual disability by affecting the development of cortical integrity.

Haploinsufficiency of MeCP2-interacting transcriptional co-repressor SIN3A causes mild intellectual disability by affecting the development of cortical integrity.

Journal: Nature genetics

Published: September 11, 2015

Microdeletions in 9q33.3-q34.11 in five patients with intellectual disability, microcephaly, and seizures of incomplete penetrance: is STXBP1 not the only causative gene?

Microdeletions in 9q33.3-q34.11 in five patients with intellectual disability, microcephaly, and seizures of incomplete penetrance: is STXBP1 not the only causative gene?

Journal: Molecular cytogenetics

Published: July 17, 2015

Array-based molecular karyotyping in fetal brain malformations: Identification of novel candidate genes and chromosomal regions.

Array-based molecular karyotyping in fetal brain malformations: Identification of novel candidate genes and chromosomal regions.

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

Published: July 01, 2015

De Novo Mutations in CHAMP1 Cause Intellectual Disability with Severe Speech Impairment.

De Novo Mutations in CHAMP1 Cause Intellectual Disability with Severe Speech Impairment.

Journal: American journal of human genetics

Published: June 08, 2015

Showing 1-12 of 21

Last Updated: 09/26/2026