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Laurent C Francioli

Showing results (1-10 of 27) with videos related to

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European Journal of Human Genetics : EJHG|May 5, 2019
Disparities in discovery of pathogenic variants for autosomal recessive non-syndromic hearing impairment by ancestryImen Chakchouk, Di Zhang, Zhihui Zhang, et al.
The Lancet. Infectious Diseases|February 24, 2022
Implementation of hand hygiene in health-care facilities: results from the WHO Hand Hygiene Self-Assessment Framework global survey 2019Marlieke E A de Kraker, Ermira Tartari, Sara Tomczyk, et al.
Nature Communications|February 3, 2021
Author Correction: Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomesQingbo Wang, Emma Pierce-Hoffman, Beryl B Cummings, et al.
Nature Communications|May 29, 2020
Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomesQingbo Wang, Emma Pierce-Hoffman, Beryl B Cummings, et al.
European Journal of Human Genetics : EJHG|November 24, 2016
A framework for the detection of de novo mutations in family-based sequencing dataLaurent C Francioli, Mircea Cretu-Stancu, Kiran V Garimella, et al.
American Journal of Human Genetics|November 20, 2015
Leveraging Distant Relatedness to Quantify Human Mutation and Gene-Conversion RatesPier Francesco Palamara, Laurent C Francioli, Peter R Wilton, et al.
Science (New York, N.Y.)|May 6, 2017
Negative selection in humans and fruit flies involves synergistic epistasisMashaal Sohail, Olga A Vakhrusheva, Jae Hoon Sul, et al.
Plos Genetics|March 8, 2013
Deleterious alleles in the human genome are on average younger than neutral alleles of the same frequencyAdam Kiezun, Sara L Pulit, Laurent C Francioli, et al.
Nature Communications|May 29, 2020
Characterising the loss-of-function impact of 5' untranslated region variants in 15,708 individualsNicola Whiffin, Konrad J Karczewski, Xiaolei Zhang, et al.
Nature Communications|February 3, 2021
Author Correction: Characterising the loss-of-function impact of 5' untranslated region variants in 15,708 individualsNicola Whiffin, Konrad J Karczewski, Xiaolei Zhang, et al.
Pageof 3

Showing results (1-10 of 27) with videos related to

Sort By:
Pageof 3
European Journal of Human Genetics : EJHG|May 5, 2019
Disparities in discovery of pathogenic variants for autosomal recessive non-syndromic hearing impairment by ancestryImen Chakchouk, Di Zhang, Zhihui Zhang, et al.
The Lancet. Infectious Diseases|February 24, 2022
Implementation of hand hygiene in health-care facilities: results from the WHO Hand Hygiene Self-Assessment Framework global survey 2019Marlieke E A de Kraker, Ermira Tartari, Sara Tomczyk, et al.
Nature Communications|February 3, 2021
Author Correction: Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomesQingbo Wang, Emma Pierce-Hoffman, Beryl B Cummings, et al.
Nature Communications|May 29, 2020
Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomesQingbo Wang, Emma Pierce-Hoffman, Beryl B Cummings, et al.
European Journal of Human Genetics : EJHG|November 24, 2016
A framework for the detection of de novo mutations in family-based sequencing dataLaurent C Francioli, Mircea Cretu-Stancu, Kiran V Garimella, et al.
American Journal of Human Genetics|November 20, 2015
Leveraging Distant Relatedness to Quantify Human Mutation and Gene-Conversion RatesPier Francesco Palamara, Laurent C Francioli, Peter R Wilton, et al.
Science (New York, N.Y.)|May 6, 2017
Negative selection in humans and fruit flies involves synergistic epistasisMashaal Sohail, Olga A Vakhrusheva, Jae Hoon Sul, et al.
Plos Genetics|March 8, 2013
Deleterious alleles in the human genome are on average younger than neutral alleles of the same frequencyAdam Kiezun, Sara L Pulit, Laurent C Francioli, et al.
Nature Communications|May 29, 2020
Characterising the loss-of-function impact of 5' untranslated region variants in 15,708 individualsNicola Whiffin, Konrad J Karczewski, Xiaolei Zhang, et al.
Nature Communications|February 3, 2021
Author Correction: Characterising the loss-of-function impact of 5' untranslated region variants in 15,708 individualsNicola Whiffin, Konrad J Karczewski, Xiaolei Zhang, et al.
Pageof 3