Bérengère de Martinville

Author

Also Known As

B de Martinville, B. De Martinville, B. Martinville, B. de Martinville, Berengere de Martinville, Berengère De Martinville, Bérengère De Martinville, Bérengère de Martinville

Publications

1.6K

Citations

H-Index

Concepts

All Affiliations

Yale University Centre Hospitalier Universitaire de Lille Massachusetts Institute of Technology Hôpital Jeanne de Flandre Université Paris Cité

About

Bérengère de Martinville is an author at Yale University specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	11	1.1K
2	Natural Sciences	4	4	373
3	Public Health	2	2	408
4	Biochemistry	2	2	70
5	Biology	1	1	11

Bérengère de Martinville

Publications

1.5K

Citations

H-Index

Page 1

	Year	Citations
Genotype-phenotype analysis in 2,405 patients with a dystrophinopathy using the UMD-DMD database: a model of nationwide knowledgebase Sylvie Tuffery‐Giraud, Christophe Béroud, France Leturcq, Human Mutation GeneticsDatabasesDiagnosisGenetic EpidemiologyPathology	2009	364
Single-copy sequence hybridizes to polymorphic and homologous loci on human X and Y chromosomes. David C. Page, Bérengère de Martinville, David Barker, Proceedings of the National Academy of Sciences CytogeneticsGeneticsDna AnalysisMolecular BiologyMolecular Genetics	1982	176
Human Ornithine Transcarbamylase Locus Mapped to Band Xp21.1 Near the Duchenne Muscular Dystrophy Locus Valerie Lindgren, Bérengère de Martinville, Arthur L. Horwich, Science Genetic AnalysisDevelopmental BiologyX Chromosome AbnormalitiesMendelian DisorderGenetic Disorder	1984	127
The Human Gene for the β Subunit of Nerve Growth Factor Is Located on the Proximal Short Arm of Chromosome 1 Uta Francke, Bérengère de Martinville, Lisa M. Coussens, Science	1983	114
Oncogene from Human EJ Bladder Carcinoma Is Located on the Short Arm of Chromosome 11 Bérengère de Martinville, Joseph C. Giacalone, Chiaho Shih, Science GeneticsPathologyMolecular GeneticsHuman Chromosome 11Tumor Biology	1983	104
Assignment of first random restriction fragment length polymorphism (RFLP) locus ((D14S1) to a region of human chromosome 14. Bérengère de Martinville, Arlene R. Wyman, R. White, PubMed	1982	77
New syndromic form of benign hereditary chorea is associated with a deletion of TITF‐1 and PAX‐9 contiguous genes David Devos, Isabelle Vuillaume, Alix de Becdelièvre, Movement Disorders	2006	76
The c-Ha-ras1, insulin and β-globin loci map outside the deletion associated with aniridia-Wilms' tumour Bérengère de Martinville, Uta Francke Nature MedicinePathologyβ-Globin Loci MapCell BiologyCancer Research	1983	71
Assignment of the human gene for muscle-type phosphofructokinase (PFKM) to chromosome 1 (region cen→q32) using somatic cell hybrids and monoclonal anti-M antibody Shobhana Vora, Susan Durham, Bérengère de Martinville, Somatic Cell and Molecular Genetics Protein ExpressionSomatic Cell GeneticsGeneticsMuscle-type PhosphofructokinaseRegion Cen→q32	1982	67
The Human Fatty Acid Transport Protein-1 (SLC27A1; FATP-1) cDNA and Gene: Organization, Chromosomal Localization, and Expression Geneviève Martin, Masami Nemoto, Laurent Gelman, Genomics Chromosomal LocalizationBiochemistryNatural SciencesMetabolic RegulationMetabolism	2000	59

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