Bi-allelic DNAH8 Variants Lead to Multiple Morphological Abnormalities of the Sperm Flagella and Primary Male Infertility

Chunyu Liu, Haruhiko Miyata, Yang Gao, +23

The American Journal of Human Genetics

BiologyInfertilityAllelic VariantCytogeneticsGenetic Disorder +13

Mutations in DNAH17, Encoding a Sperm-Specific Axonemal Outer Dynein Arm Heavy Chain, Cause Isolated Male Infertility Due to Asthenozoospermia

Marjorie Whitfield, Lucie Thomas, Émilie Béquignon, +18

The American Journal of Human Genetics

InfertilityAndrologyFertilityGeneticsSperm Biology +8

Tubulin glycylation controls axonemal dynein activity, flagellar beat, and male fertility

Sudarshan Gadadhar, Gonzalo Alvarez Viar, Jan N. Hansen, +10

Science

Mutations in TTC29, Encoding an Evolutionarily Conserved Axonemal Protein, Result in Asthenozoospermia and Male Infertility

Patrick Lorès, Denis Dacheux, Zine‐Eddine Kherraf, +33

The American Journal of Human Genetics

BiologyInfertilityAndrologyDevelopmental BiologyGenetics +6

TTC12 Loss-of-Function Mutations Cause Primary Ciliary Dyskinesia and Unveil Distinct Dynein Assembly Mechanisms in Motile Cilia Versus Flagella

Lucie Thomas, Khaled Bouhouche, Marjorie Whitfield, +30

The American Journal of Human Genetics

GeneticsMolecular GeneticsCytoskeletonMedicineCell Biology

Comprehensive overview of murine epididymal mononuclear phagocytes and lymphocytes: Unexpected populations arise

Allison Voisin, Marjorie Whitfield, Christelle Damon‐Soubeyrand, +6

Journal of Reproductive Immunology

Clinical ImmunologyInflammationLymphocyte DevelopmentGranulocyteComprehensive Overview +7

Posttesticular sperm maturation, infertility, and hypercholesterolemia

Joël R. Drevet, Marjorie Whitfield, Xavier Pollet‐Villard, +2

Asian Journal of Andrology

SpermatogenesisFertilityGynecologySemen AnalysisReproductive Biology +14

The sodium/proton exchanger <scp>SLC9C1</scp> ( <scp>sNHE</scp> ) is essential for human sperm motility and fertility

Emma Cavarocchi, Marjorie Whitfield, Ahmed Chargui, +10

Clinical Genetics

Bi-allelic truncating variants in CFAP206 cause male infertility in human and mouse

Qunshan Shen, Guillaume Martinez, Hongbin Liu, +23

Human Genetics

SpermatogenesisKnockout MouseAllelic VariantDevelopmental BiologyGenetic Disorder +7

A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet–Biedl syndrome

Patrick Lorès, Zine‐Eddine Kherraf, Amir Amiri‐Yekta, +17

Human Genetics

BiologyInfertilityGenetic DisorderGeneticsPathogenesis +9