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Nicola H Chapman

Showing results (1-10 of 17) with videos related to

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Genetics|September 21, 2002
The effect of population history on the lengths of ancestral chromosome segmentsNicola H Chapman, Elizabeth A Thompson
Human Heredity|May 9, 2006
Segregation analysis of a complex quantitative trait: approaches for identifying influential data pointsRobert P Igo, Nicola H Chapman, Ellen M Wijsman
BMC Health Services Research|September 29, 2011
Clinicians adopting evidence based guidelines: a case study with thromboprophylaxisNicola H Chapman, Steven P Lazar, Margaret Fry, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 5, 2003
Segregation analysis of phenotypic components of learning disabilities. II. Phonological decodingNicola H Chapman, Wendy H Raskind, Jennifer B Thomson, et al.
Australian Family Physician|March 14, 2009
Venous thromboembolism - management in general practiceNicola H Chapman, Timothy Brighton, Mark F Harris, et al.
Bioinformatics (Oxford, England)|August 2, 2015
PBAP: a pipeline for file processing and quality control of pedigree data with dense genetic markersAlejandro Q Nato, Nicola H Chapman, Harkirat K Sohi, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|August 30, 2025
Multi-ancestry meta-analysis identifies genetic modifiers of age-at-onset of Alzheimer's disease at known and novel lociElizabeth E Blue, Jai Broome, Diane Xue, et al.
American Journal of Human Genetics|February 19, 2026
Multiple-testing corrections in case-control studies using identity-by-descent segmentsSeth D Temple, Nicola H Chapman, Seung Hoan Choi, et al.
Biorxiv : the Preprint Server for Biology|July 17, 2025
Multiple-testing corrections in case-control studies using identity-by-descent segmentsSeth D Temple, Nicola H Chapman, Seung Hoan Choi, et al.
Behavior Genetics|July 9, 2008
Genome scan of a nonword repetition phenotype in families with dyslexia: evidence for multiple lociZoran Brkanac, Nicola H Chapman, Robert P Igo, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Genetics|September 21, 2002
The effect of population history on the lengths of ancestral chromosome segmentsNicola H Chapman, Elizabeth A Thompson
Human Heredity|May 9, 2006
Segregation analysis of a complex quantitative trait: approaches for identifying influential data pointsRobert P Igo, Nicola H Chapman, Ellen M Wijsman
BMC Health Services Research|September 29, 2011
Clinicians adopting evidence based guidelines: a case study with thromboprophylaxisNicola H Chapman, Steven P Lazar, Margaret Fry, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 5, 2003
Segregation analysis of phenotypic components of learning disabilities. II. Phonological decodingNicola H Chapman, Wendy H Raskind, Jennifer B Thomson, et al.
Australian Family Physician|March 14, 2009
Venous thromboembolism - management in general practiceNicola H Chapman, Timothy Brighton, Mark F Harris, et al.
Bioinformatics (Oxford, England)|August 2, 2015
PBAP: a pipeline for file processing and quality control of pedigree data with dense genetic markersAlejandro Q Nato, Nicola H Chapman, Harkirat K Sohi, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|August 30, 2025
Multi-ancestry meta-analysis identifies genetic modifiers of age-at-onset of Alzheimer's disease at known and novel lociElizabeth E Blue, Jai Broome, Diane Xue, et al.
American Journal of Human Genetics|February 19, 2026
Multiple-testing corrections in case-control studies using identity-by-descent segmentsSeth D Temple, Nicola H Chapman, Seung Hoan Choi, et al.
Biorxiv : the Preprint Server for Biology|July 17, 2025
Multiple-testing corrections in case-control studies using identity-by-descent segmentsSeth D Temple, Nicola H Chapman, Seung Hoan Choi, et al.
Behavior Genetics|July 9, 2008
Genome scan of a nonword repetition phenotype in families with dyslexia: evidence for multiple lociZoran Brkanac, Nicola H Chapman, Robert P Igo, et al.
Pageof 2