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Thilo Dörk

Showing results (1-10 of 316) with videos related to

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Cancers|October 23, 2021
Genomic Risk Factors for Cervical CancerDhanya Ramachandran, Thilo Dörk
Hereditary Cancer in Clinical Practice|September 13, 2013
Hereditary breast cancer: ever more pieces to the polygenic puzzleNatalia Bogdanova, Sonja Helbig, Thilo Dörk
American Journal of Obstetrics and Gynecology|January 7, 2022
Causation and causal inference in obstetrics-gynecologyOlaf Dammann, Thilo Dörk, Peter Hillemanns, et al.
American Journal of Medical Genetics. Part A|April 1, 2004
Slow progression of ataxia-telangiectasia with double missense and in frame splice mutationsThilo Dörk, Regina Bendix-Waltes, Rolf-Dieter Wegner, et al.
International Journal of Legal Medicine|January 9, 2019
Evidence for an association of interferon gene variants with sudden infant death syndromeAngelina Hafke, Peter Schürmann, Thomas Rothämel, et al.
Genes|January 8, 2025
Genetic Association Study of Acetylcholinesterase (<i>ACHE</i>) and Butyrylcholinesterase (<i>BCHE</i>) Variants in Sudden Infant Death Syndrome (SIDS)Dong Qu, Peter Schürmann, Thomas Rothämel, et al.
International Journal of Legal Medicine|July 23, 2015
Polymorphisms in genes of respiratory control and sudden infant death syndromeKatharina Läer, Thilo Dörk, Marielle Vennemann, et al.
International Journal of Legal Medicine|April 27, 2022
Variants in genes encoding the SUR1-TRPM4 non-selective cation channel and sudden infant death syndrome (SIDS): potentially increased risk for cerebral edemaDong Qu, Peter Schürmann, Thomas Rothämel, et al.
Acta Paediatrica (Oslo, Norway : 1992)|March 22, 2023
Polymorphisms of the hypothalamic-pituitary-adrenal axis may lead to an inadequate response to stress and contribute to sudden infant death syndromeElanur Uzuntas, Peter Schürmann, Thomas Rothämel, et al.
International Journal of Legal Medicine|October 31, 2020
Genetic association study of fatal pulmonary embolismLisa Meißner, Peter Schürmann, Thilo Dörk, et al.
Pageof 32

Showing results (1-10 of 316) with videos related to

Sort By:
Pageof 32
Cancers|October 23, 2021
Genomic Risk Factors for Cervical CancerDhanya Ramachandran, Thilo Dörk
Hereditary Cancer in Clinical Practice|September 13, 2013
Hereditary breast cancer: ever more pieces to the polygenic puzzleNatalia Bogdanova, Sonja Helbig, Thilo Dörk
American Journal of Obstetrics and Gynecology|January 7, 2022
Causation and causal inference in obstetrics-gynecologyOlaf Dammann, Thilo Dörk, Peter Hillemanns, et al.
American Journal of Medical Genetics. Part A|April 1, 2004
Slow progression of ataxia-telangiectasia with double missense and in frame splice mutationsThilo Dörk, Regina Bendix-Waltes, Rolf-Dieter Wegner, et al.
International Journal of Legal Medicine|January 9, 2019
Evidence for an association of interferon gene variants with sudden infant death syndromeAngelina Hafke, Peter Schürmann, Thomas Rothämel, et al.
Genes|January 8, 2025
Genetic Association Study of Acetylcholinesterase (<i>ACHE</i>) and Butyrylcholinesterase (<i>BCHE</i>) Variants in Sudden Infant Death Syndrome (SIDS)Dong Qu, Peter Schürmann, Thomas Rothämel, et al.
International Journal of Legal Medicine|July 23, 2015
Polymorphisms in genes of respiratory control and sudden infant death syndromeKatharina Läer, Thilo Dörk, Marielle Vennemann, et al.
International Journal of Legal Medicine|April 27, 2022
Variants in genes encoding the SUR1-TRPM4 non-selective cation channel and sudden infant death syndrome (SIDS): potentially increased risk for cerebral edemaDong Qu, Peter Schürmann, Thomas Rothämel, et al.
Acta Paediatrica (Oslo, Norway : 1992)|March 22, 2023
Polymorphisms of the hypothalamic-pituitary-adrenal axis may lead to an inadequate response to stress and contribute to sudden infant death syndromeElanur Uzuntas, Peter Schürmann, Thomas Rothämel, et al.
International Journal of Legal Medicine|October 31, 2020
Genetic association study of fatal pulmonary embolismLisa Meißner, Peter Schürmann, Thilo Dörk, et al.
Pageof 32