Nicolas Richard - Concepedia

Author

Nicolas Richard

Also Known As

C Kurtz, Galmiche, Guillaume, N Richard, N. Richard, Nathaniel Richard, Nicolas Richard, Richard, N Graham, Richard, N., Richard, Nadège, Richard, Nicolas

Publications

1.8K

Citations

H-Index

Concepts

All Affiliations

Université de Caen Normandie Centre Hospitalier Universitaire de Caen Normandie Inserm Assistance Publique – Hôpitaux de Paris Sorbonne Université

About

Nicolas Richard is an author at Université de Caen Normandie specializing in medicine, reproductive endocrinology, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	11	388
2	Public Health	4	4	204
3	Health Sciences	1	1	10
4	Biology	1	1	11
5	Cell Biology	1	1	140

Nicolas Richard

Publications

1.6K

Citations

H-Index

Page 1

	Year	Citations
InnateDB: facilitating systems‐level analyses of the mammalian innate immune response David J. Lynn, Geoffrey L. Winsor, Calvin C. Chan, Molecular Systems Biology	2008	386
<i>CYP24A1</i>Mutations in a Cohort of Hypercalcemic Patients: Evidence for a Recessive Trait Arnaud Molin, R. Baudoin, Martin Kaufmann, The Journal of Clinical Endocrinology & Metabolism	2015	140
KiSS‐1 and GPR54 Genes are Co‐Expressed in Rat Gonadotrophs and Differentially Regulated <i>In Vivo</i> by Oestradiol and Gonadotrophin‐Releasing Hormone Nicolas Richard, G. Galmiche, Sophie Corvaisier, Journal of Neuroendocrinology Human GrowthGeneticsRat GonadotrophsFemale Reproductive FunctionGpr54 Expression	2008	140
A New Deletion Ablating NESP55 Causes Loss of Maternal Imprint of A/B<i>GNAS</i>and Autosomal Dominant Pseudohypoparathyroidism Type Ib Nicolas Richard, Geneviève Abéguilé, Nadia Coudray, The Journal of Clinical Endocrinology & Metabolism	2012	95
Progressive Osseous Heteroplasia: A Model for the Imprinting Effects of GNAS Inactivating Mutations in Humans M. Lebrun, Nicolas Richard, Geneviève Abéguilé, The Journal of Clinical Endocrinology & Metabolism	2010	78
Paternal<i>GNAS</i>Mutations Lead to Severe Intrauterine Growth Retardation (IUGR) and Provide Evidence for a Role of XLαs in Fetal Development Nicolas Richard, Arnaud Molin, Nadia Coudray, The Journal of Clinical Endocrinology & Metabolism	2013	76
Vitamin D–Dependent Rickets Type 1B (25-Hydroxylase Deficiency): A Rare Condition or a Misdiagnosed Condition? Arnaud Molin, Arnaud Wiedemann, Nick Demers, Journal of Bone and Mineral Research	2017	71
An Apoptosis Methylation Prognostic Signature for Early Lung Cancer in the IFCT-0002 Trial Florence de Fraipont, Guénaëlle Levallet, Christian Créveuil, Clinical Cancer Research	2012	61
A new FSHβ mutation in a 29-year-old woman with primary amenorrhea and isolated FSH deficiency: functional characterization and ovarian response to human recombinant FSH Marie-Laure Kottler, Yen-Yin Chou, Olivier Chabre, European Journal of Endocrinology	2009	59
Disruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disorders Hui Guo, Elisa Bettella, Paul C. Marcogliese, Nature Communications	2019	59

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