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Michael Buckley

Showing results (111-120 of 121) with videos related to

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Scientific Reports|December 15, 2021
An infant burial from Arma Veirana in northwestern Italy provides insights into funerary practices and female personhood in early Mesolithic EuropeJamie Hodgkins, Caley M Orr, Claudine Gravel-Miguel, et al.
Molecular Genetics & Genomic Medicine|January 10, 2018
Integrating exome sequencing into a diagnostic pathway for epileptic encephalopathy: Evidence of clinical utility and cost effectivenessElizabeth E Palmer, Deborah Schofield, Rupendra Shrestha, et al.
Human Molecular Genetics|June 9, 2016
Neuronal deficiency of ARV1 causes an autosomal recessive epileptic encephalopathyElizabeth E Palmer, Kelsey E Jarrett, Rani K Sachdev, et al.
Scientific Reports|July 4, 2019
Methylome and transcriptome maps of human visceral and subcutaneous adipocytes reveal key epigenetic differences at developmental genesStephen T Bradford, Shalima S Nair, Aaron L Statham, et al.
Plos One|August 18, 2017
Reconstructing Asian faunal introductions to eastern Africa from multi-proxy biomolecular and archaeological datasetsMary E Prendergast, Michael Buckley, Alison Crowther, et al.
Human Genetics|April 3, 2021
Pathogenic variants in CDH11 impair cell adhesion and cause Teebi hypertelorism syndromeDong Li, Michael E March, Paola Fortugno, et al.
Nature Genetics|September 12, 2018
Integrative detection and analysis of structural variation in cancer genomesJesse R Dixon, Jie Xu, Vishnu Dileep, et al.
Annals of Neurology|June 5, 2025
HCN2-Associated Neurodevelopmental Disorders: Data from Patients and Xenopus Cell ModelsClara Houdayer, A Marie Phillips, Marie Chabbert, et al.
Medrxiv : the Preprint Server for Health Sciences|April 2, 2024
Mono and biallelic variants in <i>HCN2</i> cause severe neurodevelopmental disordersClara Houdayer, A Marie Phillips, Marie Chabbert, et al.
Biorxiv : the Preprint Server for Biology|April 17, 2023
The ENCODE Uniform Analysis PipelinesBenjamin C Hitz, Lee Jin-Wook, Otto Jolanki, et al.
Pageof 13

Showing results (111-120 of 121) with videos related to

Sort By:
Pageof 13
Scientific Reports|December 15, 2021
An infant burial from Arma Veirana in northwestern Italy provides insights into funerary practices and female personhood in early Mesolithic EuropeJamie Hodgkins, Caley M Orr, Claudine Gravel-Miguel, et al.
Molecular Genetics & Genomic Medicine|January 10, 2018
Integrating exome sequencing into a diagnostic pathway for epileptic encephalopathy: Evidence of clinical utility and cost effectivenessElizabeth E Palmer, Deborah Schofield, Rupendra Shrestha, et al.
Human Molecular Genetics|June 9, 2016
Neuronal deficiency of ARV1 causes an autosomal recessive epileptic encephalopathyElizabeth E Palmer, Kelsey E Jarrett, Rani K Sachdev, et al.
Scientific Reports|July 4, 2019
Methylome and transcriptome maps of human visceral and subcutaneous adipocytes reveal key epigenetic differences at developmental genesStephen T Bradford, Shalima S Nair, Aaron L Statham, et al.
Plos One|August 18, 2017
Reconstructing Asian faunal introductions to eastern Africa from multi-proxy biomolecular and archaeological datasetsMary E Prendergast, Michael Buckley, Alison Crowther, et al.
Human Genetics|April 3, 2021
Pathogenic variants in CDH11 impair cell adhesion and cause Teebi hypertelorism syndromeDong Li, Michael E March, Paola Fortugno, et al.
Nature Genetics|September 12, 2018
Integrative detection and analysis of structural variation in cancer genomesJesse R Dixon, Jie Xu, Vishnu Dileep, et al.
Annals of Neurology|June 5, 2025
HCN2-Associated Neurodevelopmental Disorders: Data from Patients and Xenopus Cell ModelsClara Houdayer, A Marie Phillips, Marie Chabbert, et al.
Medrxiv : the Preprint Server for Health Sciences|April 2, 2024
Mono and biallelic variants in <i>HCN2</i> cause severe neurodevelopmental disordersClara Houdayer, A Marie Phillips, Marie Chabbert, et al.
Biorxiv : the Preprint Server for Biology|April 17, 2023
The ENCODE Uniform Analysis PipelinesBenjamin C Hitz, Lee Jin-Wook, Otto Jolanki, et al.
Pageof 13