Bernd Auber

Carl Neuberg Str. 1
Hannover, NI 30625, Germany

Last Updated: 09/26/2026

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Found 76 publications

Human GPR174 deficiency drives polyclonal lymphoproliferative disease via defects in T cell function.

Human GPR174 deficiency drives polyclonal lymphoproliferative disease via defects in T cell function.

Journal: medRxiv : the preprint server for health sciences

Published: July 30, 2026

Multi-omics analysis in suspected hereditary breast and ovarian cancer cases reveals novel candidate susceptibility factors.

Multi-omics analysis in suspected hereditary breast and ovarian cancer cases reveals novel candidate susceptibility factors.

Journal: NPJ breast cancer

Published: May 06, 2026

Spectrum of double heterozygosity in individuals diagnosed with hereditary breast and ovarian cancer.

Spectrum of double heterozygosity in individuals diagnosed with hereditary breast and ovarian cancer.

Journal: European journal of cancer (Oxford, England : 1990)

Published: April 24, 2026

Genetic testing in prostate cancer-what the new S3 guideline means for urological practice

Genetic testing in prostate cancer-what the new S3 guideline means for urological practice

Journal: Urologie (Heidelberg, Germany)

Published: April 09, 2026

From Recommendation to Implementation: Clinical Outcomes of a Single-Center Molecular Tumor Board.

From Recommendation to Implementation: Clinical Outcomes of a Single-Center Molecular Tumor Board.

Journal: Targeted oncology

Published: February 28, 2026

Functional inactivation of MDR3 caused by a homozygous ABCB4 missense variant leading to liver failure.

Functional inactivation of MDR3 caused by a homozygous ABCB4 missense variant leading to liver failure.

Journal: Frontiers in genetics

Published: February 02, 2026

Bi-allelic WDHD1 variants cause microcephalic primordial dwarfism.

Bi-allelic WDHD1 variants cause microcephalic primordial dwarfism.

Journal: American journal of human genetics

Published: December 18, 2025

Germline variants in ATM, BRCA2, other cancer predisposition and novel candidate genes are implicated in glioma risk in adult glioma patients with a familial or personal history of tumors.

Germline variants in ATM, BRCA2, other cancer predisposition and novel candidate genes are implicated in glioma risk in adult glioma patients with a familial or personal history of tumors.

Journal: Acta neuropathologica

Published: August 26, 2025

Low lymphozyte pool, colon perforation and hydrocephalus as clinical features in an infant with a postzygotic PIK3CA variant.

Low lymphozyte pool, colon perforation and hydrocephalus as clinical features in an infant with a postzygotic PIK3CA variant.

Journal: Frontiers in pediatrics

Published: June 19, 2025

Presentation of Patients With Congenital Anomalies of the Kidney and Urinary Tract and PAX2 Loss-of-Function Variants and Implications for Clinical Management.

Presentation of Patients With Congenital Anomalies of the Kidney and Urinary Tract and PAX2 Loss-of-Function Variants and Implications for Clinical Management.

Journal: Kidney international reports

Published: June 06, 2025

Tandem duplication and triplication in BRCA1: revisiting the large genomic rearrangements via optical genome mapping.

Tandem duplication and triplication in BRCA1: revisiting the large genomic rearrangements via optical genome mapping.

Journal: Cancer genetics

Published: May 28, 2025

Shwachman-Diamond syndrome due to biallelic EFL1 variants with complex and fatal clinical course in early infancy.

Shwachman-Diamond syndrome due to biallelic EFL1 variants with complex and fatal clinical course in early infancy.

Journal: British journal of haematology

Published: June 25, 2024

Showing 1-12 of 76

Last Updated: 09/26/2026