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Cordula Haas

Showing results (11-20 of 79) with videos related to

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Seizure|December 22, 2023
Response to the letter from Josef Finsterer regarding our article "Exome analysis focusing on epilepsy-related genes in children and adults with sudden unexplained death"Sarah E Buerki, Cordula Haas, Jacqueline Neubauer
Seizure|November 23, 2023
Exome analysis focusing on epilepsy-related genes in children and adults with sudden unexplained deathSarah E Buerki, Cordula Haas, Jacqueline Neubauer
Forensic Science International|December 9, 2021
19th century family saga re-told by DNA recovered from postcard stampsCordula Haas, Christian Körner, Andrea Sulzer, et al.
Forensic Science International. Genetics|April 5, 2022
Source level interpretation of mixed biological stains using coding region SNPsGuro Dørum, Øyvind Bleka, Peter Gill, et al.
Aging|July 21, 2025
The influence of cancer on a forensic age estimation toolCharlotte Sutter, Daniel Helbling, Cordula Haas, et al.
Forensic Science International|December 12, 2024
Methylation-based forensic age estimation in blood, buccal cells, saliva and semen: A comparison of two technologiesCharlotte Sutter, Yael Marti, Cordula Haas, et al.
Legal Medicine (Tokyo, Japan)|March 6, 2009
No association of serotonin transporter gene variation with sudden infant death syndrome (SIDS) in CaucasiansCordula Haas, Julia Braun, Walter Bär, et al.
International Journal of Legal Medicine|April 25, 2021
Re-evaluation of single nucleotide variants and identification of structural variants in a cohort of 45 sudden unexplained death casesJacqueline Neubauer, Shouyu Wang, Giancarlo Russo, et al.
Forensic Science International. Genetics|August 31, 2019
Transcription and microbial profiling of body fluids using a massively parallel sequencing approachAndrea Patrizia Salzmann, Giancarlo Russo, Sirisha Aluri, et al.
Heartrhythm Case Reports|June 20, 2018
Functional implications of a rare variant in the sodium channel β1B subunit (<i>SCN1B</i>) in a 5-month-old male sudden infant death syndrome caseJacqueline Neubauer, Jean-Sébastien Rougier, Hugues Abriel, et al.
Pageof 8

Showing results (11-20 of 79) with videos related to

Sort By:
Pageof 8
Seizure|December 22, 2023
Response to the letter from Josef Finsterer regarding our article "Exome analysis focusing on epilepsy-related genes in children and adults with sudden unexplained death"Sarah E Buerki, Cordula Haas, Jacqueline Neubauer
Seizure|November 23, 2023
Exome analysis focusing on epilepsy-related genes in children and adults with sudden unexplained deathSarah E Buerki, Cordula Haas, Jacqueline Neubauer
Forensic Science International|December 9, 2021
19th century family saga re-told by DNA recovered from postcard stampsCordula Haas, Christian Körner, Andrea Sulzer, et al.
Forensic Science International. Genetics|April 5, 2022
Source level interpretation of mixed biological stains using coding region SNPsGuro Dørum, Øyvind Bleka, Peter Gill, et al.
Aging|July 21, 2025
The influence of cancer on a forensic age estimation toolCharlotte Sutter, Daniel Helbling, Cordula Haas, et al.
Forensic Science International|December 12, 2024
Methylation-based forensic age estimation in blood, buccal cells, saliva and semen: A comparison of two technologiesCharlotte Sutter, Yael Marti, Cordula Haas, et al.
Legal Medicine (Tokyo, Japan)|March 6, 2009
No association of serotonin transporter gene variation with sudden infant death syndrome (SIDS) in CaucasiansCordula Haas, Julia Braun, Walter Bär, et al.
International Journal of Legal Medicine|April 25, 2021
Re-evaluation of single nucleotide variants and identification of structural variants in a cohort of 45 sudden unexplained death casesJacqueline Neubauer, Shouyu Wang, Giancarlo Russo, et al.
Forensic Science International. Genetics|August 31, 2019
Transcription and microbial profiling of body fluids using a massively parallel sequencing approachAndrea Patrizia Salzmann, Giancarlo Russo, Sirisha Aluri, et al.
Heartrhythm Case Reports|June 20, 2018
Functional implications of a rare variant in the sodium channel β1B subunit (<i>SCN1B</i>) in a 5-month-old male sudden infant death syndrome caseJacqueline Neubauer, Jean-Sébastien Rougier, Hugues Abriel, et al.
Pageof 8