Fabienne Clot

Hla types in celiac disease patients not carrying the DQA1*05-DQB1*02 (DQ2) heterodimer: results from the european genetics cluster on celiac disease

Kati Karell, A.S. Louka, Simon Moodie et al. · Human Immunology · 2003 · 613 citations

Life Sciences, Genetics, Immunology +17

Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study

Isabelle Le Ber, Agnès Camuzat, Didier Hannequin et al. · Brain · 2008 · 349 citations

Life Sciences, Genetics, Neurology +17

Genome Search in Celiac Disease

Luigi Greco, Gino Roberto Corazza, Marie‐Claude Babron et al. · The American Journal of Human Genetics · 1998 · 211 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

Homozygous GRN mutations: new phenotypes and new insights into pathological and molecular mechanisms

Vincent Huin, Mathieu Barbier, Armand Bottani et al. · Brain · 2019 · 94 citations · Full text

Medicine, Genetics, Neurology +17

Bilateral Deep Brain Stimulation of the Pallidum for Myoclonus-Dystonia Due to ε-Sarcoglycan Mutations

Julie Azoulay-Zyss, Emmanuel Roze, Marie‐Laure Welter et al. · Archives of Neurology · 2011 · 90 citations

Medicine, Neurology, Surgery +15