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Matthew E Hurles

Showing results (111-120 of 190) with videos related to

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Nature Genetics|May 25, 2023
The impact of rare protein coding genetic variation on adult cognitive functionChia-Yen Chen, Ruoyu Tian, Tian Ge, et al.
Nature Communications|October 13, 2019
Contribution of retrotransposition to developmental disordersEugene J Gardner, Elena Prigmore, Giuseppe Gallone, et al.
Nature Communications|January 28, 2021
The contribution of X-linked coding variation to severe developmental disordersHilary C Martin, Eugene J Gardner, Kaitlin E Samocha, et al.
Nature Communications|August 9, 2020
Dynamic changes in the epigenomic landscape regulate human organogenesis and link to developmental disordersDave T Gerrard, Andrew A Berry, Rachel E Jennings, et al.
Nature|January 10, 2020
A brief history of human disease geneticsMelina Claussnitzer, Judy H Cho, Rory Collins, et al.
American Journal of Human Genetics|December 25, 2012
Genomic pathology of SLE-associated copy-number variation at the FCGR2C/FCGR3B/FCGR2B locusMichael Mueller, Paula Barros, Abigail S Witherden, et al.
American Journal of Human Genetics|January 29, 2013
Genetic basis of Y-linked hearing impairmentQiuju Wang, Yali Xue, Yujun Zhang, et al.
American Journal of Human Genetics|February 20, 2003
The genetic legacy of the MongolsTatiana Zerjal, Yali Xue, Giorgio Bertorelle, et al.
American Journal of Human Genetics|October 2, 2012
Recessive HYDIN mutations cause primary ciliary dyskinesia without randomization of left-right body asymmetryHeike Olbrich, Miriam Schmidts, Claudius Werner, et al.
Nature Biotechnology|May 10, 2011
Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variantsDalila Pinto, Katayoon Darvishi, Xinghua Shi, et al.
Pageof 19

Showing results (111-120 of 190) with videos related to

Sort By:
Pageof 19
Nature Genetics|May 25, 2023
The impact of rare protein coding genetic variation on adult cognitive functionChia-Yen Chen, Ruoyu Tian, Tian Ge, et al.
Nature Communications|October 13, 2019
Contribution of retrotransposition to developmental disordersEugene J Gardner, Elena Prigmore, Giuseppe Gallone, et al.
Nature Communications|January 28, 2021
The contribution of X-linked coding variation to severe developmental disordersHilary C Martin, Eugene J Gardner, Kaitlin E Samocha, et al.
Nature Communications|August 9, 2020
Dynamic changes in the epigenomic landscape regulate human organogenesis and link to developmental disordersDave T Gerrard, Andrew A Berry, Rachel E Jennings, et al.
Nature|January 10, 2020
A brief history of human disease geneticsMelina Claussnitzer, Judy H Cho, Rory Collins, et al.
American Journal of Human Genetics|December 25, 2012
Genomic pathology of SLE-associated copy-number variation at the FCGR2C/FCGR3B/FCGR2B locusMichael Mueller, Paula Barros, Abigail S Witherden, et al.
American Journal of Human Genetics|January 29, 2013
Genetic basis of Y-linked hearing impairmentQiuju Wang, Yali Xue, Yujun Zhang, et al.
American Journal of Human Genetics|February 20, 2003
The genetic legacy of the MongolsTatiana Zerjal, Yali Xue, Giorgio Bertorelle, et al.
American Journal of Human Genetics|October 2, 2012
Recessive HYDIN mutations cause primary ciliary dyskinesia without randomization of left-right body asymmetryHeike Olbrich, Miriam Schmidts, Claudius Werner, et al.
Nature Biotechnology|May 10, 2011
Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variantsDalila Pinto, Katayoon Darvishi, Xinghua Shi, et al.
Pageof 19