Catherine Dodé


Ontology type: schema:Person     


Person Info

NAME

Catherine

SURNAME

Dodé

Publications in SciGraph latest 50 shown

  • 2017-12 First mutation in the FSHR cytoplasmic tail identified in a non-pregnant woman with spontaneous ovarian hyperstimulation syndrome in BMC MEDICAL GENETICS
  • 2017-12 Next-generation sequencing of patients with congenital anosmia in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2015-09 Expert consensus document: European Consensus Statement on congenital hypogonadotropic hypogonadism—pathogenesis, diagnosis and treatment in NATURE REVIEWS ENDOCRINOLOGY
  • 2013-09 Custom oligonucleotide array-based CGH: a reliable diagnostic tool for detection of exonic copy-number changes in multiple targeted genes in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2012-03 Neonatal gonadotropin therapy in male congenital hypogonadotropic hypogonadism in NATURE REVIEWS ENDOCRINOLOGY
  • 2009-02 Kallmann syndrome in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2008-07 Biallelic mutations in the prokineticin-2 gene in two sporadic cases of Kallmann syndrome in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2007-09 Dramatic etanercept-induced remission of relapsing febrile sciatic neuralgia related to p46l mutation of the tnfrsf1a gene in CLINICAL RHEUMATOLOGY
  • 2006-06 Intestinal Pseudo-Obstruction as a Manifestation of Tumor Necrosis Factor Receptor–Associated Periodic Syndrome in DIGESTIVE DISEASES AND SCIENCES
  • 2004-11 Kallmann syndrome: fibroblast growth factor signaling insufficiency? in JOURNAL OF MOLECULAR MEDICINE
  • 2004-06 Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16 in NEUROGENETICS
  • 2003-04 Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome in NATURE GENETICS
  • 2001-05 Autosomal-dominant periodic fever with AA amyloidosis: Novel mutation in tumor necrosis factor receptor 1 gene Rapid Communication in KIDNEY INTERNATIONAL
  • 2001-01 Familial Mediterranean fever in Lebanon: mutation spectrum, evidence for cases in Maronites, Greek orthodoxes, Greek catholics, Syriacs and Chiites and for an association between amyloidosis and M694V and M694I mutations in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 1989-08 Autosomal dominant polycystic kidney disease and α−4.2 thalassemia in a Caucasian family in HUMAN GENETICS
  • 1988-02 Analysis of crossover type in the α-3·7 haplotype among sickle cell anemia patients from various parts of Africa in HUMAN GENETICS
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