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Heide Fier

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

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Bioinformatics (Oxford, England)|March 24, 2017
Identification of genetic outliers due to sub-structure and cryptic relationshipsDaniel Schlauch, Heide Fier, Christoph Lange
Genetic Epidemiology|September 25, 2014
A novel method for detecting association between DNA methylation and diseases using spatial informationWai-Ki Yip, Heide Fier, Dawn L DeMeo, et al.
Immunogenetics|April 8, 2017
Mutational profiling in the peripheral blood leukocytes of patients with systemic mast cell activation syndrome using next-generation sequencingJanine Altmüller, Britta Haenisch, Amit Kawalia, et al.
Bioinformatics (Oxford, England)|November 23, 2013
On the simultaneous association analysis of large genomic regions: a massive multi-locus association testDandi Qiao, Michael H Cho, Heide Fier, et al.
Bioinformatics (Oxford, England)|October 10, 2012
'Location, Location, Location': a spatial approach for rare variant analysis and an application to a study on non-syndromic cleft lip with or without cleft palateHeide Fier, Sungho Won, Dmitry Prokopenko, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|April 8, 2014
Nonsyndromic cleft lip with or without cleft palate: Increased burden of rare variants within Gremlin-1, a component of the bone morphogenetic protein 4 pathwayTaofik Al Chawa, Kerstin U Ludwig, Heide Fier, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 27, 2015
Investigation of the role of TCF4 rare sequence variants in schizophreniaF Buket Basmanav, Andreas J Forstner, Heide Fier, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|October 20, 2012
Resequencing of VAX1 in patients with nonsyndromic cleft lip with or without cleft palateEntessar Nasser, Elisabeth Mangold, Daniela C Tradowsky, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|November 22, 2019
Shared Genetic Etiology of Obesity-Related Traits and Barrett's Esophagus/Adenocarcinoma: Insights from Genome-Wide Association StudiesAnne C Böhmer, Julian Hecker, Julia Schröder, et al.
Plos One|February 7, 2017
Identification of shared risk loci and pathways for bipolar disorder and schizophreniaAndreas J Forstner, Julian Hecker, Andrea Hofmann, et al.
Pageof 1

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

Sort By:
Pageof 1
Bioinformatics (Oxford, England)|March 24, 2017
Identification of genetic outliers due to sub-structure and cryptic relationshipsDaniel Schlauch, Heide Fier, Christoph Lange
Genetic Epidemiology|September 25, 2014
A novel method for detecting association between DNA methylation and diseases using spatial informationWai-Ki Yip, Heide Fier, Dawn L DeMeo, et al.
Immunogenetics|April 8, 2017
Mutational profiling in the peripheral blood leukocytes of patients with systemic mast cell activation syndrome using next-generation sequencingJanine Altmüller, Britta Haenisch, Amit Kawalia, et al.
Bioinformatics (Oxford, England)|November 23, 2013
On the simultaneous association analysis of large genomic regions: a massive multi-locus association testDandi Qiao, Michael H Cho, Heide Fier, et al.
Bioinformatics (Oxford, England)|October 10, 2012
'Location, Location, Location': a spatial approach for rare variant analysis and an application to a study on non-syndromic cleft lip with or without cleft palateHeide Fier, Sungho Won, Dmitry Prokopenko, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|April 8, 2014
Nonsyndromic cleft lip with or without cleft palate: Increased burden of rare variants within Gremlin-1, a component of the bone morphogenetic protein 4 pathwayTaofik Al Chawa, Kerstin U Ludwig, Heide Fier, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 27, 2015
Investigation of the role of TCF4 rare sequence variants in schizophreniaF Buket Basmanav, Andreas J Forstner, Heide Fier, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|October 20, 2012
Resequencing of VAX1 in patients with nonsyndromic cleft lip with or without cleft palateEntessar Nasser, Elisabeth Mangold, Daniela C Tradowsky, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|November 22, 2019
Shared Genetic Etiology of Obesity-Related Traits and Barrett's Esophagus/Adenocarcinoma: Insights from Genome-Wide Association StudiesAnne C Böhmer, Julian Hecker, Julia Schröder, et al.
Plos One|February 7, 2017
Identification of shared risk loci and pathways for bipolar disorder and schizophreniaAndreas J Forstner, Julian Hecker, Andrea Hofmann, et al.
Pageof 1