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Joëlle Augé

Observed names: Joelle Auge, Joelle Augé, Joelle Augé, Joëlle Auge
OpenAlex ID: A5111749971
PAX8,TITF1, andFOXE1Gene Expression Patterns during Human Development: New Insights into Human Thyroid Development and Thyroid Dysgenesis-Associated Malformations
2005 · Sylvia Sura Trueba, Joëlle Augé, et al. · The Journal of Clinical Endocrinology & Metabolism · 227
Truncating Neurotrypsin Mutation in Autosomal Recessive Nonsyndromic Mental Retardation
2002 · Florence Molinari, Marlène Rio, et al. · Science · 190
Neurological Phenotype in Waardenburg Syndrome Type 4 Correlates with Novel SOX10 Truncating Mutations and Expression in Developing Brain
2000 · Renaud L. Touraine, Tania Attié-Bitach, et al. · The American Journal of Human Genetics · 173
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Antenatal Presentation of Bardet-Biedl Syndrome May Mimic Meckel Syndrome
2005 · Houda Karmous-Benailly, Jelena Martinovic, et al. · The American Journal of Human Genetics · 137
PAX2 mutations in renal–coloboma syndrome: mutational hotspot and germline mosaicism
2000 · Jeanne Amiel, Sophie Audollent, et al. · European Journal of Human Genetics · 83
Expression of the Sonic Hedgehog gene in human embryos with neural tube defects
2000 · Irena Kirillova, Irena Novikova, et al. · Teratology · 48
Gene expression in pharyngeal arch 1 during human embryonic development
2005 · Juanliang Cai, David Ash, et al. · Human Molecular Genetics · 46
Expression of the SMADIP1 gene during early human development
2002 · Yolanda Espinosa-Parrilla, Jeanne Amiel, et al. · Mechanisms of Development · 44
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Salvage of 5′-deoxy-5′-methylthioadenosine and L-homocysteine into methionine in cells cultured in a methionine-free medium: A study of “methionine-dependence”
1986 · Laurence Christa, Joëlle Kersual, et al. · Biochemical and Biophysical Research Communications · 22
Works count: 9
Citation count: 970
H-index: 9
I10-index: 9
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