Thomas Karaouzène - Concepedia

Concepedia

Author

Thomas Karaouzène

Centre National de la Recherche Scientifique

Also Known As

Karaouzene, Thomas, Thomas Karaouzene, Thomas Karaouzène

17

Publications

1.8K

Citations

14

H-Index

46

Concepts

All Affiliations

Centre National de la Recherche Scientifique Université Grenoble Alpes Centre Hospitalier Universitaire de Grenoble Inserm Translational Innovation in Medicine and Complexity

TK

About

Thomas Karaouzène is an author at Centre National de la Recherche Scientifique specializing in medicine, male infertility, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	1.1K
2	Public Health	7	7	986
3	Cell Biology	4	4	287
4	Biology	3	3	742
5	Natural Sciences	1	1	75

Thomas Karaouzène

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14

Publications

1.8K

Citations

14

H-Index

	Year	Citations
Mutations in DNAH1, which Encodes an Inner Arm Heavy Chain Dynein, Lead to Male Infertility from Multiple Morphological Abnormalities of the Sperm Flagella Mariem Ben Khelifa, Charles Coutton, Raoudha Zouari, The American Journal of Human Genetics BiologyChromatinInfertilityGeneticsSperm Biology	2013	464
Mutations in CFAP43 and CFAP44 cause male infertility and flagellum defects in Trypanosoma and human Charles Coutton, Alexandra Vargas, Amir Amiri‐Yekta, Nature Communications	2018	233
Absence of CFAP69 Causes Male Infertility due to Multiple Morphological Abnormalities of the Flagella in Human and Mouse Frederick N. Dong, Amir Amiri‐Yekta, Guillaume Martinez, The American Journal of Human Genetics BiologyInfertilityAndrologyFertilityGenetics	2018	167
Homozygous mutation of PLCZ1 leads to defective human oocyte activation and infertility that is not rescued by the WW-binding protein PAWP Jessica Escoffier, Hoi Chang Lee, Sandra Yassine, Human Molecular Genetics SpermatogenesisOocyteFertilityOocyte ActivationGenetics	2015	143
Whole-exome sequencing of familial cases of multiple morphological abnormalities of the sperm flagella (MMAF) reveals new<i>DNAH1</i>mutations Amir Amiri‐Yekta, Charles Coutton, Zine‐Eddine Kherraf, Human Reproduction	2016	123
<scp>SPINK</scp> 2 deficiency causes infertility by inducing sperm defects in heterozygotes and azoospermia in homozygotes Zine‐Eddine Kherraf, Marie Christou‐Kent, Thomas Karaouzène, EMBO Molecular Medicine	2017	121
Whole-exome sequencing identifies mutations in FSIP2 as a recurrent cause of multiple morphological abnormalities of the sperm flagella Guillaume Martinez, Zine‐Eddine Kherraf, Raoudha Zouari, Human Reproduction	2018	116
A Homozygous Ancestral SVA-Insertion-Mediated Deletion in WDR66 Induces Multiple Morphological Abnormalities of the Sperm Flagellum and Male Infertility Zine‐Eddine Kherraf, Amir Amiri‐Yekta, Denis Dacheux, The American Journal of Human Genetics BiologyInfertilityDevelopmental BiologyFertilitySperm Flagellum	2018	111
Subcellular localization of phospholipase Cζ in human sperm and its absence in DPY19L2-deficient sperm are consistent with its role in oocyte activation Jessica Escoffier, Sandra Yassine, Hoi Chang Lee, Molecular Human Reproduction	2014	90
<scp>PATL</scp> 2 is a key actor of oocyte maturation whose invalidation causes infertility in women and mice Marie Christou‐Kent, Zine‐Eddine Kherraf, Amir Amiri‐Yekta, EMBO Molecular Medicine	2018	89

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