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Karl Skorecki

Showing results (121-130 of 134) with videos related to

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Nature Communications|December 19, 2013
Phylogenetic applications of whole Y-chromosome sequences and the Near Eastern origin of Ashkenazi LevitesSiiri Rootsi, Doron M Behar, Mari Järve, et al.
Scientific Reports|November 4, 2017
The genetic variation in the R1a clade among the Ashkenazi Levites' Y chromosomeDoron M Behar, Lauri Saag, Monika Karmin, et al.
Clinical Kidney Journal|April 13, 2019
G1 is the major <i>APOL1</i> risk allele for hypertension-attributed nephropathy in Central AfricaErnest K Sumaili, Revital Shemer, Etty Kruzel-Davila, et al.
American Journal of Human Genetics|December 9, 2008
The genetic legacy of religious diversity and intolerance: paternal lineages of Christians, Jews, and Muslims in the Iberian PeninsulaSusan M Adams, Elena Bosch, Patricia L Balaresque, et al.
The Journal of Investigative Dermatology|March 23, 2012
Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgarisOfer Sarig, Sivan Bercovici, Lilach Zoller, et al.
Kidney International Reports|October 18, 2023
Diagnostic Utility of Exome Sequencing Among Israeli Children With Kidney FailureYishay Ben-Moshe, Omer Shlomovitz, Danit Atias-Varon, et al.
Human Biology|August 1, 2014
No evidence from genome-wide data of a Khazar origin for the Ashkenazi JewsDoron M Behar, Mait Metspalu, Yael Baran, et al.
Kidney International Reports|April 30, 2025
Genetic Terminal Complement Deficiency in Israeli Bedouins With Kidney FailureGuy Chowers, Dror Ben-Ruby, Danit Atias-Varon, et al.
American Journal of Medical Genetics. Part A|August 26, 2021
Ancestral patterns of recessive dystrophic epidermolysis bullosa mutations in Hispanic populations suggest sephardic ancestryEmily Mira Warshauer, Adam Brown, Ignacia Fuentes, et al.
Journal of Medical Genetics|September 24, 2025
Sephardic origins revealed for rare skin disorder, recessive dystrophic epidermolysis bullosa, in individuals carrying the unique c.6527insC mutationEmily Mira Warshauer, Paul A Maier, Goran Runfeldt, et al.
Pageof 14

Showing results (121-130 of 134) with videos related to

Sort By:
Pageof 14
Nature Communications|December 19, 2013
Phylogenetic applications of whole Y-chromosome sequences and the Near Eastern origin of Ashkenazi LevitesSiiri Rootsi, Doron M Behar, Mari Järve, et al.
Scientific Reports|November 4, 2017
The genetic variation in the R1a clade among the Ashkenazi Levites' Y chromosomeDoron M Behar, Lauri Saag, Monika Karmin, et al.
Clinical Kidney Journal|April 13, 2019
G1 is the major <i>APOL1</i> risk allele for hypertension-attributed nephropathy in Central AfricaErnest K Sumaili, Revital Shemer, Etty Kruzel-Davila, et al.
American Journal of Human Genetics|December 9, 2008
The genetic legacy of religious diversity and intolerance: paternal lineages of Christians, Jews, and Muslims in the Iberian PeninsulaSusan M Adams, Elena Bosch, Patricia L Balaresque, et al.
The Journal of Investigative Dermatology|March 23, 2012
Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgarisOfer Sarig, Sivan Bercovici, Lilach Zoller, et al.
Kidney International Reports|October 18, 2023
Diagnostic Utility of Exome Sequencing Among Israeli Children With Kidney FailureYishay Ben-Moshe, Omer Shlomovitz, Danit Atias-Varon, et al.
Human Biology|August 1, 2014
No evidence from genome-wide data of a Khazar origin for the Ashkenazi JewsDoron M Behar, Mait Metspalu, Yael Baran, et al.
Kidney International Reports|April 30, 2025
Genetic Terminal Complement Deficiency in Israeli Bedouins With Kidney FailureGuy Chowers, Dror Ben-Ruby, Danit Atias-Varon, et al.
American Journal of Medical Genetics. Part A|August 26, 2021
Ancestral patterns of recessive dystrophic epidermolysis bullosa mutations in Hispanic populations suggest sephardic ancestryEmily Mira Warshauer, Adam Brown, Ignacia Fuentes, et al.
Journal of Medical Genetics|September 24, 2025
Sephardic origins revealed for rare skin disorder, recessive dystrophic epidermolysis bullosa, in individuals carrying the unique c.6527insC mutationEmily Mira Warshauer, Paul A Maier, Goran Runfeldt, et al.
Pageof 14