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Anthony Musolf

Showing results (1-10 of 7) with videos related to

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BMC Proceedings|December 19, 2014
Mapping genes with longitudinal phenotypes via Bayesian posterior probabilitiesAnthony Musolf, Alejandro Q Nato, Douglas Londono, et al.
Human Heredity|April 19, 2013
Single-variant and multi-variant trend tests for genetic association with next-generation sequencing that are robust to sequencing errorWonkuk Kim, Douglas Londono, Lisheng Zhou, et al.
Genes|September 23, 2022
<i>TBX3</i> and <i>EFNA4</i> Variant in a Family with Ulnar-Mammary Syndrome and Sagittal CraniosynostosisMoon Ley Tung, Bharatendu Chandra, Jaclyn Kotlarek, et al.
Journal of Neurosurgery|November 26, 2022
A likely HOXC4 predisposition variant for Chiari malformationsDouglas L Brockmeyer, Samuel H Cheshier, Jeff Stevens, et al.
Statistical Applications in Genetics and Molecular Biology|March 19, 2013
A novel method for analyzing genetic association with longitudinal phenotypesDouglas Londono, Kuo-mei Chen, Anthony Musolf, et al.
Molecular and Cellular Biology|July 2, 2014
Chromatin profiling reveals regulatory network shifts and a protective role for hepatocyte nuclear factor 4α during colitisSanjay Chahar, Vishal Gandhi, Shiyan Yu, et al.
American Journal of Human Genetics|September 27, 2016
REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense VariantsNilah M Ioannidis, Joseph H Rothstein, Vikas Pejaver, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
BMC Proceedings|December 19, 2014
Mapping genes with longitudinal phenotypes via Bayesian posterior probabilitiesAnthony Musolf, Alejandro Q Nato, Douglas Londono, et al.
Human Heredity|April 19, 2013
Single-variant and multi-variant trend tests for genetic association with next-generation sequencing that are robust to sequencing errorWonkuk Kim, Douglas Londono, Lisheng Zhou, et al.
Genes|September 23, 2022
<i>TBX3</i> and <i>EFNA4</i> Variant in a Family with Ulnar-Mammary Syndrome and Sagittal CraniosynostosisMoon Ley Tung, Bharatendu Chandra, Jaclyn Kotlarek, et al.
Journal of Neurosurgery|November 26, 2022
A likely HOXC4 predisposition variant for Chiari malformationsDouglas L Brockmeyer, Samuel H Cheshier, Jeff Stevens, et al.
Statistical Applications in Genetics and Molecular Biology|March 19, 2013
A novel method for analyzing genetic association with longitudinal phenotypesDouglas Londono, Kuo-mei Chen, Anthony Musolf, et al.
Molecular and Cellular Biology|July 2, 2014
Chromatin profiling reveals regulatory network shifts and a protective role for hepatocyte nuclear factor 4α during colitisSanjay Chahar, Vishal Gandhi, Shiyan Yu, et al.
American Journal of Human Genetics|September 27, 2016
REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense VariantsNilah M Ioannidis, Joseph H Rothstein, Vikas Pejaver, et al.
Pageof 1