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N Feingold

Affiliation : Inserm · Château de Longchamp

• 1Publications (affiliation in France)
• 104Total publications
• 1864Citations
• 22h-index

OpenAlex

Research profile

N Feingold has 1 indexed publication (1994). Their work appears in “Human Molecular Genetics”. Their most cited article, “Localization of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping” (1994), has been cited 196 times. Their work is co-authored with at least 12 researchers.

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Research areas

• Genetic Associations and Epidemiology
• Forensic and Genetic Research
• Genetic diversity and population structure
• Renal Transplantation Outcomes and Treatments
• Lymphoma Diagnosis and Treatment

Publications (1)

• Localization of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping
  1994 · Human Molecular Genetics · cited 196 times

Collaborations

Partner institutions : Genethon (France) · Centre National de la Recherche Scientifique · Hôpital Saint-Vincent-de-Paul · Hôpital Raymond-Poincaré · Fondation Jean Dausset-CEPH

Co-authors

• Sabine Fauré
• Jean-Francols Pellissier
• M. C. Routon
• Michel Fardeau
• Fernando M. S. Tomé
• Annie Barols
• Patricia Legos
• Nuchanard Chiannllkulchaï
• Pascale Guicheney
• Laurent Grinas
• Jacques Samuel Beckmann
• Teresinha Evangelista

Bibliographic data from OpenAlex (open database).