Cheng Xu

Congenital hypogonadotropic hypogonadism and constitutional delay of growth and puberty have distinct genetic architectures

Daniele Cassatella, Sasha Howard, James S. Acierno et al. · European Journal of Endocrinology · 2018 · 131 citations · Full text

Medicine, Endocrinology, Genetics +13

KLB, encoding β‐Klotho, is mutated in patients with congenital hypogonadotropic hypogonadism

Cheng Xu, Andrea Messina, Emmanuel Somm et al. · EMBO Molecular Medicine · 2017 · 92 citations · Full text

Life Sciences, Endocrinology, Genetics +17

Defective AMH signaling disrupts GnRH neuron development and function and contributes to hypogonadotropic hypogonadism

Samuel A. Malone, Georgios Papadakis, Andrea Messina et al. · eLife · 2019 · 77 citations · Full text

Medicine, Endocrinology, Genetics +17

Congenital hypogonadotropic hypogonadism with split hand/foot malformation: a clinical entity with a high frequency of FGFR1 mutations

Carine Villanueva, Elka Jacobson-Dickman, Cheng Xu et al. · Genetics in Medicine · 2014 · 74 citations · Full text

Medicine, Endocrinology, Genetics +11

Developing and evaluating rare disease educational materials co-created by expert clinicians and patients: the paradigm of congenital hypogonadotropic hypogonadism

Corin Badiu, Marco Bonomi, Ivan Borshchevsky et al. · Orphanet Journal of Rare Diseases · 2017 · 68 citations · Full text

Education, Educational Assessment, Pediatrics +13