Martina Baumgartner-Witsch

Innsbruck, Austria

Last Updated: 09/26/2026

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Found 34 publications

Identification of a Druggable Target That Predicts Postoperative Crohn's Disease Recurrence.

Identification of a Druggable Target That Predicts Postoperative Crohn's Disease Recurrence.

Journal: Gastroenterology

Published: May 01, 2025

Retrospective identification of the first cord blood-transplanted severe aplastic anemia in a STAT1-associated chronic mucocutaneous candidiasis family: case report, review of literature and pathophysiologic background.

Retrospective identification of the first cord blood-transplanted severe aplastic anemia in a STAT1-associated chronic mucocutaneous candidiasis family: case report, review of literature and pathophysiologic background.

Journal: Frontiers in immunology

Published: May 10, 2024

Filling the gap: Genetic risk assessment in hypercholesterolemia using LDL-C and LPA genetic scores.

Filling the gap: Genetic risk assessment in hypercholesterolemia using LDL-C and LPA genetic scores.

Journal: Clinical genetics

Published: March 22, 2023

Amp(1q) and tetraploidy are commonly acquired chromosomal abnormalities in relapsed multiple myeloma.

Amp(1q) and tetraploidy are commonly acquired chromosomal abnormalities in relapsed multiple myeloma.

Journal: European journal of haematology

Published: August 20, 2022

Array genotyping as diagnostic approach in medical genetics.

Array genotyping as diagnostic approach in medical genetics.

Journal: Molecular genetics & genomic medicine

Published: May 21, 2022

Identifying adult hypophosphatasia in the rheumatology unit.

Identifying adult hypophosphatasia in the rheumatology unit.

Journal: Orphanet journal of rare diseases

Published: March 16, 2022

Genotype-Phenotype Comparison in POGZ-Related Neurodevelopmental Disorders by Using Clinical Scoring.

Genotype-Phenotype Comparison in POGZ-Related Neurodevelopmental Disorders by Using Clinical Scoring.

Journal: Genes

Published: December 20, 2021

A polymorphic AT-repeat causes frequent allele dropout for an MME mutational hotspot exon.

A polymorphic AT-repeat causes frequent allele dropout for an MME mutational hotspot exon.

Journal: Journal of medical genetics

Published: October 20, 2021

Reply to Lao Q and Merke DP.

Reply to Lao Q and Merke DP.

Journal: European journal of human genetics : EJHG

Published: March 10, 2021

Clonal dynamics in a composite chronic lymphocytic leukemia and hairy cell leukemia-variant.

Clonal dynamics in a composite chronic lymphocytic leukemia and hairy cell leukemia-variant.

Journal: Genes, chromosomes & cancer

Published: September 25, 2020

Correction to: Expanding the phenotype of hypomaturation amelogenesis imperfecta due to a novel SLC24A4 variant.

Correction to: Expanding the phenotype of hypomaturation amelogenesis imperfecta due to a novel SLC24A4 variant.

Journal: Clinical oral investigations

Published: September 08, 2020

Andrological findings in infertile men with two (biallelic) CFTR mutations: results of a multicentre study in Germany and Austria comprising 71 patients.

Andrological findings in infertile men with two (biallelic) CFTR mutations: results of a multicentre study in Germany and Austria comprising 71 patients.

Journal: Human reproduction (Oxford, England)

Published: July 06, 2020

Showing 1-12 of 34

Last Updated: 09/26/2026