Julien Philippe - Concepedia

Author

Julien Philippe

Centre National de la Recherche Scientifique ORCID

Also Known As

C. Meier, J Philippe, J. PHILIPPE, J. Philippe, J.M. Philippe, Julien PHILIPPE, Julien Philippe, Philippe, J., Philippe, J. (Julien), Philippe, Julien

181

Publications

1.4K

Citations

H-Index

Concepts

All Affiliations

Centre National de la Recherche Scientifique Institut Pasteur de Lille Université de Lille Imperial College London Université Paris Cité

About

Julien Philippe is an author at Centre National de la Recherche Scientifique specializing in medicine, diabetes, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	462
2	Engineering	2	2	63
3	Business	1	1	15
4	Health Sciences	1	1	23
5	Management	1	1	15

Julien Philippe

Publications

1.3K

Citations

H-Index

Page 1

	Year	Citations
Whole-Exome Sequencing and High Throughput Genotyping Identified KCNJ11 as the Thirteenth MODY Gene Amélie Bonnefond, Julien Philippe, Emmanuelle Durand, PLoS ONE	2012	203
Insulin regulation of the glucagon gene is mediated by an insulin-responsive DNA element. Julien Philippe Proceedings of the National Academy of Sciences Insulin DeficiencyGeneticsMolecular BiologyInsulin-responsive Dna ElementInsulin Signaling	1991	142
Genetic variants in <i>LEP</i>, <i>LEPR</i>, and <scp><i>MC4R</i></scp> explain 30% of severe obesity in children from a consanguineous population Sadia Saeed, Amélie Bonnefond, Jaida Manzoor, Obesity	2015	115
Acoustofluidic rotational tweezing enables high-speed contactless morphological phenotyping of zebrafish larvae Chuyi Chen, Yuyang Gu, Julien Philippe, Nature Communications	2021	95
Loss-of-function mutations in MRAP2 are pathogenic in hyperphagic obesity with hyperglycemia and hypertension Morgane Baron, Julie O’Sullivan Maillet, Marlène Huyvaert, Nature Medicine ObesityMetabolic SyndromeMetabolic DisorderDiabetesAutophagy	2019	91
Highly Sensitive Diagnosis of 43 Monogenic Forms of Diabetes or Obesity Through One-Step PCR-Based Enrichment in Combination With Next-Generation Sequencing Amélie Bonnefond, Julien Philippe, Emmanuelle Durand, Diabetes Care	2013	81
A nonsense loss-of-function mutation in PCSK1 contributes to dominantly inherited human obesity Julien Philippe, Pieter Stijnen, David Meyre, International Journal of Obesity ObesityMetabolic SyndromeNonsense Loss-of-function MutationSignal TransductionSignaling Pathway	2014	73
A truncating mutation in CEP55 is the likely cause of MARCH, a novel syndrome affecting neuronal mitosis Patrick Frosk, Heleen H. Arts, Julien Philippe, Journal of Medical Genetics	2017	61
Novel <i>LEPR</i> mutations in obese Pakistani children identified by PCR‐based enrichment and next generation sequencing Sadia Saeed, Amélie Bonnefond, Jaida Manzoor, Obesity	2013	60
Transcription factor gene MNX1 is a novel cause of permanent neonatal diabetes in a consanguineous family Amélie Bonnefond, Emmanuel Vaillant, Julien Philippe, Diabetes & Metabolism Developmental BiologyNovel CauseGeneticsDiabetesMedicine	2013	56

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