Susanne Stemmler

Bochum, NW, Germany

Last Updated: 09/26/2026

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Found 11 publications

The serotonin receptor 2A (HTR2A) rs6313 variant is associated with higher ongoing pain and signs of central sensitization in neuropathic pain patients.

The serotonin receptor 2A (HTR2A) rs6313 variant is associated with higher ongoing pain and signs of central sensitization in neuropathic pain patients.

Journal: European journal of pain (London, England)

Published: February 04, 2020

Trying to understand the genetics of atopic dermatitis.

Trying to understand the genetics of atopic dermatitis.

Journal: Molecular and cellular probes

Published: August 31, 2016

Prospective Evaluation of Predictive DNA Testing for Huntington's Disease in a Large German Center.

Prospective Evaluation of Predictive DNA Testing for Huntington's Disease in a Large German Center.

Journal: Journal of genetic counseling

Published: July 28, 2016

Genetic Counselling for Predictive Testing in Huntington's Disease in One Centre since 1993. Gender-Specific Aspects of Decision-Making.

Genetic Counselling for Predictive Testing in Huntington's Disease in One Centre since 1993. Gender-Specific Aspects of Decision-Making.

Journal: Journal of Huntington's disease

Published: September 04, 2015

Early-onset leukoencephalopathy due to a homozygous missense mutation in the DARS2 gene.

Early-onset leukoencephalopathy due to a homozygous missense mutation in the DARS2 gene.

Journal: Molecular and cellular probes

Published: April 22, 2015

Unravelling the complex genetic background of atopic dermatitis: from genetic association results towards novel therapeutic strategies.

Unravelling the complex genetic background of atopic dermatitis: from genetic association results towards novel therapeutic strategies.

Journal: Archives of dermatological research

Published: November 12, 2014

Association of variation in the LAMA3 gene, encoding the alpha-chain of laminin 5, with atopic dermatitis in a German case-control cohort.

Association of variation in the LAMA3 gene, encoding the alpha-chain of laminin 5, with atopic dermatitis in a German case-control cohort.

Journal: BMC dermatology

Published: June 03, 2014

The Alu-rich genomic architecture of SPAST predisposes to diverse and functionally distinct disease-associated CNV alleles.

The Alu-rich genomic architecture of SPAST predisposes to diverse and functionally distinct disease-associated CNV alleles.

Journal: American journal of human genetics

Published: April 25, 2014

Mutation and association analyses of the candidate genes ESR1, ESR2, MAX, PCNA, and KAT2A in patients with unexplained MSH2-deficient tumors.

Mutation and association analyses of the candidate genes ESR1, ESR2, MAX, PCNA, and KAT2A in patients with unexplained MSH2-deficient tumors.

Journal: Familial cancer

Published: November 17, 2011

Variation in genes of the epidermal differentiation complex in German atopic dermatitis patients.

Variation in genes of the epidermal differentiation complex in German atopic dermatitis patients.

Journal: International journal of immunogenetics

Published: July 16, 2009

Association of interleukin-8 receptor alpha polymorphisms with chronic obstructive pulmonary disease and asthma.

Association of interleukin-8 receptor alpha polymorphisms with chronic obstructive pulmonary disease and asthma.

Journal: Genes and immunity

Published: March 18, 2005

Showing 1-11 of 11

Last Updated: 09/26/2026