Jean‐Pierre de Villartay

Author

Also Known As

De Villartay, Jean-Pierre, J P De Villartay, J P de Villartay, J-P de Villartay, J. De Villartay, J. P. De Villartay, J. P. Villartay, J. P. de Villartay, J. de Villartay, J.-P. de Villartay

224

Publications

13.7K

Citations

H-Index

107

Concepts

All Affiliations

Inserm Hôpital Necker-Enfants Malades Université Paris Cité Délégation Paris 5 Assistance Publique – Hôpitaux de Paris

About

Jean‐Pierre de Villartay is an author at Inserm specializing in medicine, immunology, and cell biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	35	57	6.5K
2	Natural Sciences	15	15	899
3	Health Sciences	3	3	50
4	Allergy	3	3	289
5	Engineering	1	1	74

Jean‐Pierre de Villartay

125

Publications

12.6K

Citations

H-Index

Page 1

	Year	Citations
Mutations in Fas Associated with Human Lymphoproliferative Syndrome and Autoimmunity Frédéric Rieux‐Laucat, Françoise Le Deist, Claire Hivroz, Science GeneticsApoptosisImmunologyPathologyCell Death	1995	1.3K
Sustained Correction of X-Linked Severe Combined Immunodeficiency by ex Vivo Gene Therapy Salima Hacein‐Bey‐Abina, Frédérique Carlier, Cécile Bouneaud, New England Journal of Medicine	2002	1K
Artemis, a Novel DNA Double-Strand Break Repair/V(D)J Recombination Protein, Is Mutated in Human Severe Combined Immune Deficiency Despina Moshous, Isabelle Callebaut, Régina de Chasseval, Cell Primary ImmunodeficiencyIs MutatedGenome InstabilityImmunogeneticsAutoimmune Disease	2001	893
Cernunnos, a Novel Nonhomologous End-Joining Factor, Is Mutated in Human Immunodeficiency with Microcephaly Dietke Buck, Laurent Malivert, Régina de Chasseval, Cell Primary ImmunodeficiencyIs MutatedMedicineImmunodeficienciesImmunology	2006	697
Impairment of immunity to <i>Candida</i> and <i>Mycobacterium</i> in humans with bi-allelic <i>RORC</i> mutations Satoshi Okada, Janet Markle, Elissa K. Deenick, Science	2015	410
Long-term outcome after hematopoietic stem cell transplantation of a single-center cohort of 90 patients with severe combined immunodeficiency Bénédicte Neven, Sandrine Leroy, Hélène Decaluwe, Blood	2009	244
Partial T and B lymphocyte immunodeficiency and predisposition to lymphoma in patients with hypomorphic mutations in Artemis Despina Moshous, Christophe Pannetier, Régina de Chasseval, Journal of Clinical Investigation	2003	223
Identical mutations in RAG1 or RAG2 genes leading to defective V(D)J recombinase activity can cause either T-B–severe combined immune deficiency or Omenn syndrome Barbara Corneo, Despina Moshous, Tayfun Güngör, Blood	2001	214
Severe combined immunodeficiency and microcephaly in siblings with hypomorphic mutations in DNA ligase IV Dietke Buck, Despina Moshous, Régina de Chasseval, European Journal of Immunology Dna Double-strand BreaksMixed-phenotype Acute LeukemiaImmunodeficienciesGeneticsImmunology	2005	200
A novel immunodeficiency associated with hypomorphic RAG1 mutations and CMV infection Jean‐Pierre de Villartay Journal of Clinical Investigation	2005	194

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