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Showing 51–74 of 74 results

Advanced filters: Author: Arif B Ekici Clear advanced filters

Associations between genetic risk variants for kidney diseases and kidney disease etiology

Sebastian Wunnenburger
Ulla T. Schultheiss
Matthias Wuttke
ResearchOpen Access24 Oct 2017
Scientific Reports

Volume: 7, P: 1-7
Susceptibility gene mutations in germline and tumors of patients with HER2-negative advanced breast cancer

Peter A. Fasching
Chunling Hu
Fergus J. Couch
ResearchOpen Access13 Jul 2024
npj Breast Cancer

Volume: 10, P: 1-7
Single-cell RNA sequencing of adult mouse testes

Soeren Lukassen
Elisabeth Bosch
Andreas Winterpacht
ResearchOpen Access11 Sept 2018
Scientific Data

Volume: 5, P: 1-7
Roflumilast inhibits tumor growth and migration in STK11/LKB1 deficient pancreatic cancer

Shuman Zhang
Duo Yun
Christian Pilarsky
ResearchOpen Access09 Mar 2024
Cell Death Discovery

Volume: 10, P: 1-12
PAX5 biallelic genomic alterations define a novel subgroup of B-cell precursor acute lymphoblastic leukemia

Lorenz Bastian
Michael P. Schroeder
Claudia D. Baldus
Research06 Mar 2019
Leukemia

Volume: 33, P: 1895-1909
Genome-wide UPD screening in patients with intellectual disability

Christopher Schroeder
Arif Bülent Ekici
Michael Bonin
Research07 May 2014
European Journal of Human Genetics

Volume: 22, P: 1233-1235
Impaired ATF3 signaling involves SNAP25 in SOD1 mutant ALS patients

Volkan Yazar
Julia K. Kühlwein
Karin M. Danzer
ResearchOpen Access25 Jul 2023
Scientific Reports

Volume: 13, P: 1-13
HLA-G and HLA-F protein isoform expression in breast cancer patients receiving neoadjuvant treatment

Franziska M. Wuerfel
Hanna Huebner
Matthias Ruebner
ResearchOpen Access25 Sept 2020
Scientific Reports

Volume: 10, P: 1-10
Loss of PHF6 leads to aberrant development of human neuron-like cells

Anna Fliedner
Anne Gregor
Christiane Zweier
ResearchOpen Access04 Nov 2020
Scientific Reports

Volume: 10, P: 1-15
Neutral sphingomyelinase mediates the co-morbidity trias of alcohol abuse, major depression and bone defects

Liubov S. Kalinichenko
Christiane Mühle
Christian P. Müller
ResearchOpen Access28 Sept 2021
Molecular Psychiatry

Volume: 26, P: 7403-7416
Germline variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis

Maria Escala-Garcia
Sander Canisius
Marjanka K. Schmidt
ResearchOpen Access05 Oct 2021
Scientific Reports

Volume: 11, P: 1-11
Need for high-resolution Genetic Analysis in iPSC: Results and Lessons from the ForIPS Consortium

Bernt Popp
Mandy Krumbiegel
André Reis
ResearchOpen Access21 Nov 2018
Scientific Reports

Volume: 8, P: 1-14
The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

Gisella Figlioli
Massimo Bogliolo
Paolo Peterlongo
ResearchOpen Access01 Nov 2019
npj Breast Cancer

Volume: 5, P: 1-14
Genetic interaction screen for severe neurodevelopmental disorders reveals a functional link between Ube3a and Mef2 in Drosophila melanogaster

Jonas Straub
Anne Gregor
Christiane Zweier
ResearchOpen Access27 Jan 2020
Scientific Reports

Volume: 10, P: 1-12
DYNC2LI1 mutations broaden the clinical spectrum of dynein-2 defects

Kristin Kessler
Ina Wunderlich
Christian T. Thiel
ResearchOpen Access01 Jul 2015
Scientific Reports

Volume: 5, P: 1-12
Evolutionary conserved networks of human height identify multiple Mendelian causes of short stature

Nadine N. Hauer
Bernt Popp
Christian T. Thiel
ResearchOpen Access26 Feb 2019
European Journal of Human Genetics

Volume: 27, P: 1061-1071
A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24

Simon Gayther and colleagues report a genome wide association study for ovarian cancer. They identify two new susceptibility loci at 2q31 and 8q24 and two suggestive susceptibility loci at 3q25 and 17q21.

Ellen L Goode
Georgia Chenevix-Trench
Paul D P Pharoah
Research19 Sept 2010
Nature Genetics

Volume: 42, P: 874-879
Genome-wide association study of germline variants and breast cancer-specific mortality

Maria Escala-Garcia
Qi Guo
Marjanka K. Schmidt
ResearchOpen Access21 Feb 2019
British Journal of Cancer

Volume: 120, P: 647-657
Exome Pool-Seq in neurodevelopmental disorders

Bernt Popp
Arif B. Ekici
Christiane Zweier
ResearchOpen Access20 Nov 2017
European Journal of Human Genetics

Volume: 25, P: 1364-1376
Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1

Timothy HT Cheng
Deborah Thompson
Ian Tomlinson
ResearchOpen Access01 Dec 2015
Scientific Reports

Volume: 5, P: 1-12
Clinical and experimental evidence suggest a link between KIF7 and C5orf42-related ciliopathies through Sonic Hedgehog signaling

Reza Asadollahi
Justin E Strauss
Anita Rauch
ResearchOpen Access10 Jan 2018
European Journal of Human Genetics

Volume: 26, P: 197-209
Genome-wide association study with DNA pooling identifies variants at CNTNAP2 associated with pseudoexfoliation syndrome

Mandy Krumbiegel
Francesca Pasutto
André Reis
Research01 Sept 2010
European Journal of Human Genetics

Volume: 19, P: 186-193
Association of mineral and bone biomarkers with adverse cardiovascular outcomes and mortality in the German Chronic Kidney Disease (GCKD) cohort

Katharina Charlotte Reimer
Jennifer Nadal
Wolfram Gronwald
ResearchOpen Access20 Oct 2023
Bone Research

Volume: 11, P: 1-8
Clinical relevance of systematic phenotyping and exome sequencing in patients with short stature

Nadine N Hauer
Bernt Popp
Christian T Thiel
ResearchOpen Access12 Oct 2017
Genetics in Medicine

Volume: 20, P: 630-638

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Associations between genetic risk variants for kidney diseases and kidney disease etiology

Susceptibility gene mutations in germline and tumors of patients with HER2-negative advanced breast cancer

Single-cell RNA sequencing of adult mouse testes

Roflumilast inhibits tumor growth and migration in STK11/LKB1 deficient pancreatic cancer

PAX5 biallelic genomic alterations define a novel subgroup of B-cell precursor acute lymphoblastic leukemia

Genome-wide UPD screening in patients with intellectual disability

Impaired ATF3 signaling involves SNAP25 in SOD1 mutant ALS patients

HLA-G and HLA-F protein isoform expression in breast cancer patients receiving neoadjuvant treatment

Loss of PHF6 leads to aberrant development of human neuron-like cells

Neutral sphingomyelinase mediates the co-morbidity trias of alcohol abuse, major depression and bone defects

Germline variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis

Need for high-resolution Genetic Analysis in iPSC: Results and Lessons from the ForIPS Consortium

The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

Genetic interaction screen for severe neurodevelopmental disorders reveals a functional link between Ube3a and Mef2 in Drosophila melanogaster

DYNC2LI1 mutations broaden the clinical spectrum of dynein-2 defects

Evolutionary conserved networks of human height identify multiple Mendelian causes of short stature

A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24

Genome-wide association study of germline variants and breast cancer-specific mortality

Exome Pool-Seq in neurodevelopmental disorders

Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1

Clinical and experimental evidence suggest a link between KIF7 and C5orf42-related ciliopathies through Sonic Hedgehog signaling

Genome-wide association study with DNA pooling identifies variants at CNTNAP2 associated with pseudoexfoliation syndrome

Association of mineral and bone biomarkers with adverse cardiovascular outcomes and mortality in the German Chronic Kidney Disease (GCKD) cohort

Clinical relevance of systematic phenotyping and exome sequencing in patients with short stature

Search

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