Get started
Author

Serge Pissard

Observed names: Pissard, Serge, S Pissard, S. Pissard, Serge PISSARD
Observed institutions: Hôpital Necker-Enfants Malades, Inserm, Institut Pasteur, Université Paris-Est Créteil, Centre Hospitalier Universitaire de Bordeaux, Centre Hospitalier Universitaire Henri-Mondor, Institut Necker Enfants Malades, Laboratory of Excellence GR-Ex, Assistance Publique – Hôpitaux de Paris, Hôpital Pellegrin, Centre Pasteur du Cameroun, Hôpital Robert-Debré, Hôpitaux Universitaires Henri-Mondor, Centre Hospitalier Régional Universitaire de Brest, IRCCS Ospedale San Raffaele, Hôpital Saint Eloi, Hôpital Antoine-Béclère, Hôpital Albert-Chenevier, Institut Mondor de Recherche Biomédicale, Hôpital de la Timone, Bicêtre Hospital, Université Paris Diderot, Laboratoire d'hématologie, Pôle de recherche et d'enseignement supérieur Université Paris-Est, University of Blida
ORCID: 0000-0002-1557-4766
Observed ORCID: 0000-0002-1557-4766
OpenAlex ID: A5019836697
FGFR3 and TP53 gene mutations define two distinct pathways in urothelial cell carcinoma of the bladder.
2003 · Ashraf A Bakkar, Herve Wallerand, et al. · PubMed · 269
Does Liebig's law of the minimum scale up from species to communities?
2008 · Michael Danger, Tanguy Daufresne, et al. · Oikos · 237
PDF
Erythrocyte density in sickle cell syndromes is associated with specific clinical manifestations and hemolysis
2012 · Pablo Bartolucci, Carlo Brugnara, et al. · Blood · 133
PDF
Pathophysiology of sickle cell disease is mirrored by the red blood cell metabolome
2010 · Dhouha Darghouth, Bérengère Koehl, et al. · Blood · 132
PDF
Clinically relevant updates of the HbVar database of human hemoglobin variants and thalassemia mutations
2020 · Belinda M Giardine, Philippe Joly, et al. · Nucleic Acids Research · 124
PDF
Hydroxyurea can eliminate transfusion requirements in children with severe β-thalassemia
2003 · Mohamed Bradai, Mohand Tayeb Abad, et al. · Blood · 118
Addressing the diagnostic gaps in pyruvate kinase deficiency: Consensus recommendations on the diagnosis of pyruvate kinase deficiency
2018 · Paola Bianchi, Elisa Fermo, et al. · American Journal of Hematology · 100
PDF
Comparison of Immunocytochemical and Molecular Features with the Phenotype in a Case of Incomplete Male Pseudohermaphroditism Associated with a Mutation of the Luteinizing Hormone Receptor
1997 · M. Misrahi, G. Meduri, et al. · The Journal of Clinical Endocrinology & Metabolism · 99
One hundred spots parallel monitoring of DNA interactions by SPR imaging of polymer-functionalized surfaces applied to the detection of cystic fibrosis mutations
2003 · Nathalie Bassil, Emmanuel Maillart, et al. · Sensors and Actuators B Chemical · 84
Variants in genetic modifiers of -thalassemia can help to predict the major or intermedia type of the disease
2011 · C. Badens, P. Joly, et al. · Haematologica · 78
PDF
Selection of Maternal Human Immunodeficiency Virus Type 1 Variants in Human Placenta
1999 · Elisabeth Menu, François‐Xavier M'bopi Kéou, et al. · The Journal of Infectious Diseases · 75
Decreased transfusion needs associated with hydroxyurea therapy in Algerian patients with thalassemia major or intermedia
2007 · Mohamed Bradai, Serge Pissard, et al. · Transfusion · 69
PDF
Unstable Alpha Hemoglobin Stabilizing Protein as a Cause of Thalassemia: Proof of Concept.
2009 · Serge Pissard, Corinne Vasseur, et al. · Blood · 67
Haematological determinants of cardiac involvement in adults with sickle cell disease
2015 · Thibaud Damy, Diane Bodez, et al. · European Heart Journal · 66
A potential regulatory region for the expression of fetal hemoglobin in sickle cell disease
1994 · S Pissard, Y Beuzard · Blood · 63
PDF
Comprehensive functional annotation of 18 missense mutations found in suspected hemochromatosis type 4 patients
2014 · I. Callebaut, R. Joubrel, et al. · Human Molecular Genetics · 60
Pyruvate kinase deficiency in France: a 3‐year study reveals 27 new mutations
2006 · Serge Pissard, Isabelle Max‐Audit, et al. · British Journal of Haematology · 58
A genetic score for the prediction of beta-thalassemia severity
2014 · F. Danjou, M. Francavilla, et al. · Haematologica · 56
PDF
Validation of a reverse-hybridization StripAssay for the simultaneous analysis of common α-thalassemia point mutations and deletions
2007 · Helene Puehringer, Hossein Najmabadi, et al. · Clinical Chemistry and Laboratory Medicine (CCLM) · 45
Homozygous Southeast Asian ovalocytosis is a severe dyserythropoietic anemia associated with distal renal tubular acidosis
2014 · Véronique Picard, Alexis Proust, et al. · Blood · 44
Biological impact of α genes, β haplotypes, and G6PD activity in sickle cell anemia at baseline and with hydroxyurea
2018 · Françoise Bernaudin, Cécile Arnaud, et al. · Blood Advances · 35
Rapid Detection of β-Thalassemia Alleles in Egypt Using Naturally or Amplified Created Restriction Sites and Direct Sequencing: A Step in Disease Control
2007 · Gehan Hussein, Manal Fawzy, et al. · Hemoglobin · 35
Exome sequencing for diagnosis of congenital hemolytic anemia
2020 · Lamisse Mansour-Hendili, Abdelrazak Aissat, et al. · Orphanet Journal of Rare Diseases · 32
PDF
Variability of hemoglobin F expression in hemoglobin EE disease: Hematological and molecular analysis
2014 · Naruwat Pakdee, Supawadee Yamsri, et al. · Blood Cells Molecules and Diseases · 32
A new gene associated with a β-thalassemia phenotype: the observation of variants in SUPT5H
2020 · Ahlem Achour, Tamara Koopmann, et al. · Blood · 26
PDF
Works count: 137
Citation count: 2,756
H-index: 26
I10-index: 52
Year
Topic
Type