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Neil A Hanchard

Showing results (11-20 of 67) with videos related to

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American Journal of Human Genetics|December 19, 2003
Evidence for extensive transmission distortion in the human genomeSebastian Zöllner, Xiaoquan Wen, Neil A Hanchard, et al.
Transfusion|December 7, 2017
Whole-exome sequencing of sickle cell disease patients with hyperhemolysis syndrome suggests a role for rare variation in disease predispositionSavannah Mwesigwa, Joann M Moulds, Alice Chen, et al.
Pediatric Neurology|August 22, 2017
Clinical Metabolomics to Segregate Aromatic Amino Acid Decarboxylase Deficiency From Drug-Induced Metabolite ElevationsKirk L Pappan, Adam D Kennedy, Pilar L Magoulas, et al.
BMC Medical Genetics|April 26, 2011
UGT1A1 sequence variants and bilirubin levels in early postnatal life: a quantitative approachNeil A Hanchard, Jennifer Skierka, Amy Weaver, et al.
Nature Reviews. Endocrinology|April 16, 2026
Precision medicine in low-income settings and small island developing statesSushant Saluja, Fahmida Mannan, Guillaume Pare, et al.
Frontiers in Genetics|June 25, 2019
Hydroxyurea-Induced miRNA Expression in Sickle Cell Disease Patients in AfricaKhuthala Mnika, Gaston K Mazandu, Mario Jonas, et al.
Medrxiv : the Preprint Server for Health Sciences|January 7, 2025
Common and rare genetic variation intersects with ancestry to influence human skin and plasma carotenoid concentrationsYixing Han, Savannah Mwesigwa, Qiang Wu, et al.
American Journal of Human Genetics|December 31, 2005
Screening for recently selected alleles by analysis of human haplotype similarityNeil A Hanchard, Kirk A Rockett, Chris Spencer, et al.
Molecular Genetics and Metabolism|March 20, 2016
Functional cellular analyses reveal energy metabolism defect and mitochondrial DNA depletion in a case of mitochondrial aconitase deficiencyRoa Sadat, Emanuele Barca, Ruchi Masand, et al.
Plos One|January 17, 2009
Genetic variation on chromosome 6 influences F cell levels in healthy individuals of African descent and HbF levels in sickle cell patientsLisa E Creary, Pinar Ulug, Stephan Menzel, et al.
Pageof 7

Showing results (11-20 of 67) with videos related to

Sort By:
Pageof 7
American Journal of Human Genetics|December 19, 2003
Evidence for extensive transmission distortion in the human genomeSebastian Zöllner, Xiaoquan Wen, Neil A Hanchard, et al.
Transfusion|December 7, 2017
Whole-exome sequencing of sickle cell disease patients with hyperhemolysis syndrome suggests a role for rare variation in disease predispositionSavannah Mwesigwa, Joann M Moulds, Alice Chen, et al.
Pediatric Neurology|August 22, 2017
Clinical Metabolomics to Segregate Aromatic Amino Acid Decarboxylase Deficiency From Drug-Induced Metabolite ElevationsKirk L Pappan, Adam D Kennedy, Pilar L Magoulas, et al.
BMC Medical Genetics|April 26, 2011
UGT1A1 sequence variants and bilirubin levels in early postnatal life: a quantitative approachNeil A Hanchard, Jennifer Skierka, Amy Weaver, et al.
Nature Reviews. Endocrinology|April 16, 2026
Precision medicine in low-income settings and small island developing statesSushant Saluja, Fahmida Mannan, Guillaume Pare, et al.
Frontiers in Genetics|June 25, 2019
Hydroxyurea-Induced miRNA Expression in Sickle Cell Disease Patients in AfricaKhuthala Mnika, Gaston K Mazandu, Mario Jonas, et al.
Medrxiv : the Preprint Server for Health Sciences|January 7, 2025
Common and rare genetic variation intersects with ancestry to influence human skin and plasma carotenoid concentrationsYixing Han, Savannah Mwesigwa, Qiang Wu, et al.
American Journal of Human Genetics|December 31, 2005
Screening for recently selected alleles by analysis of human haplotype similarityNeil A Hanchard, Kirk A Rockett, Chris Spencer, et al.
Molecular Genetics and Metabolism|March 20, 2016
Functional cellular analyses reveal energy metabolism defect and mitochondrial DNA depletion in a case of mitochondrial aconitase deficiencyRoa Sadat, Emanuele Barca, Ruchi Masand, et al.
Plos One|January 17, 2009
Genetic variation on chromosome 6 influences F cell levels in healthy individuals of African descent and HbF levels in sickle cell patientsLisa E Creary, Pinar Ulug, Stephan Menzel, et al.
Pageof 7