Radu Harbuz

A Recurrent Deletion of DPY19L2 Causes Infertility in Man by Blocking Sperm Head Elongation and Acrosome Formation

Radu Harbuz, Raoudha Zouari, Virginie Pierre et al. · The American Journal of Human Genetics · 2011 · 197 citations · Full text

Veterinary Medicine, Genetics, Molecular Genetics +14

The Aurora Kinase C c.144delC mutation causes meiosis I arrest in men and is frequent in the North African population

Raoudha Zouari, Radu Harbuz, François Vialard et al. · Human Molecular Genetics · 2009 · 108 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

A new AURKC mutation causing macrozoospermia: implications for human spermatogenesis and clinical diagnosis

Mariem Ben Khelifa, Raoudha Zouari, Radu Harbuz et al. · Molecular Human Reproduction · 2011 · 80 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Refining the regulatory region upstream of <i>SOX9</i> associated with 46,XX testicular disorders of Sex Development (DSD)

Capucine Hyon, Sandra Chantot‐Bastaraud, Radu Harbuz et al. · American Journal of Medical Genetics Part A · 2015 · 62 citations · Full text

Medicine, Genetics, Molecular Genetics +16

<i>PBX1</i> haploinsufficiency leads to syndromic congenital anomalies of the kidney and urinary tract (CAKUT) in humans

Pauline Le Tanno, Julie Breton, Marie Bidart et al. · Journal of Medical Genetics · 2017 · 60 citations

Medicine, Genetics, Molecular Genetics +17