Hanène Landolsi

Mutations Causing Familial Biparental Hydatidiform Mole Implicate C6orf221 as a Possible Regulator of Genomic Imprinting in the Human Oocyte

David Parry, Clare V. Logan, Bruce E. Hayward et al. · The American Journal of Human Genetics · 2011 · 250 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Semen Parameters and Sperm DNA Fragmentation as Causes of Recurrent Pregnancy Loss

Sonia Brahem, Meriem Mehdi, Hanène Landolsi et al. · Urology · 2011 · 105 citations

Medicine, Obstetrics, Urology +16

Report of four new patients with protein-truncating mutations in C6orf221/KHDC3L and colocalization with NLRP7

Ramesh Reddy, Elie Akoury, Ngoc Minh Nguyen et al. · European Journal of Human Genetics · 2012 · 81 citations

Medicine, Genetics, Molecular Genetics +4

Celiac disease in Tunisia: serological screening in healthy blood donors

Amani Mankaï, Hanène Landolsi, A. Chahed et al. · Pathologie Biologie · 2005 · 39 citations

Life Sciences, Immunology, Autoimmunity +15

Cytogenetic and Molecular Aspects of Absolute Teratozoospermia: Comparison Between Polymorphic and Monomorphic Forms

Sonia Brahem, Hatem Elghezal, Houda Ghédir et al. · Urology · 2011 · 31 citations

Life Sciences, Genetics, Molecular Genetics +9