Concepedia

Author

Paquita Nurden

Hôpital Xavier ArnozanORCID

Also Known As

Alan Nurden, Alasdair Parker, Andrew Mumford, Bellinger, Dwight A., E. Fressinaud, Gisèle Clofent-Sanchez, John Pasi, Karyn Megy, Mattia Frontini, NURDEN, Paquita

278

Publications

16.5K

Citations

66

H-Index

124

Concepts

All Affiliations

Hôpital Xavier ArnozanCentre National de la Recherche ScientifiqueInsermLille’s Cardiology HospitalPlateforme Technologique d'Innovation Biomédicale
PN

About

Paquita Nurden is an author at Hôpital Xavier Arnozan specializing in medicine, hematology, and thrombosis.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

28

48

5.8K

2

Health Sciences

3

3

692

3

Public Health

3

3

180

4

Natural Sciences

1

1

65

5

Allergy

1

1

10

Paquita Nurden

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126

Publications

11K

Citations

54

H-Index

YearCitations

Identification of the platelet ADP receptor targeted by antithrombotic drugs

Gunther Hollopeter, Hans‐Michael Jantzen, D Vincent,

Nature

2001

1.4K

Recommendations for the standardization of light transmission aggregometry: a consensus of the working party from the platelet physiology subcommittee of SSC/ISTH

Marco Cattaneo, Chiara Cerletti, Paul Harrison,

Journal of Thrombosis and Haemostasis

2013

535

Autologous preparations rich in growth factors promote proliferation and induce VEGF and HGF production by human tendon cells in culture

Eduardo Anitua, Isabel Andí, Mikel Sánchez,

Journal of Orthopaedic Research®

2004

501

Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease

Keren Carss, Gavin Arno, Marie Erwood,

The American Journal of Human Genetics

2016

463

Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome

Cornelis A. Albers, Dirk S. Paul, Harald Schulze,

Nature Genetics

2012

419

Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome

Cornelis A. Albers, Ana Cvejic, Rémi Favier,

Nature Genetics

2011

274

Lethal hemophagocytic lymphohistiocytosis in Hermansky-Pudlak syndrome type II

Anselm Enders, Barbara Zieger, Klaus Schwarz,

Blood

2006

212

An inherited bleeding disorder linked to a defective interaction between ADP and its receptor on platelets. Its influence on glycoprotein IIb-IIIa complex function.

Paquita Nurden, Pierre Savi, E Heilmann,

Journal of Clinical Investigation

1995

202

Thrombocytopenia-associated mutations in the ANKRD26 regulatory region induce MAPK hyperactivation

Dominique Bluteau, Alessandra Balduini, Nathalie Balayn,

Journal of Clinical Investigation

2014

201

Gray platelet syndrome and defective thrombo-inflammation in Nbeal2-deficient mice

Carsten Deppermann, Deya Cherpokova, Paquita Nurden,

Journal of Clinical Investigation

2013

197

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