L. Kéclard

Association of UGT1A1 polymorphism with prevalence and age at onset of cholelithiasis in sickle cell anemia.

Vicky Chaar, L. Kéclard, Jean Pierre Diara et al. · PubMed · 2005 · 69 citations

Medicine, Genetics, Molecular Genetics +17

<i>UGT1A1</i> polymorphism outweighs the modest effect of deletional (−3.7 kb) α‐thalassemia on cholelithogenesis in sickle cell anemia

Vicky Chaar, L. Kéclard, Maryse Etienne‐Julan et al. · American Journal of Hematology · 2006 · 29 citations · Full text

Life Sciences, Genetics, Hematology +15

β^sHaplotypes, α-Globin Gene Status, and Hematological Data of Sickle Cell Disease Patients in Guadeloupe (F.W.I.)

L. Kéclard, V. Ollendorf, C Berchel et al. · Hemoglobin · 1996 · 27 citations

Life Sciences, Genetics, Hematology +12

Sickle cell disorder, β-globin gene cluster haplotypes and α-thalassemia in neonates and adults from Guadeloupe

L. Kéclard, Marc Romana, E. Lavocat et al. · American Journal of Hematology · 1997 · 26 citations · Full text

Life Sciences, Genetics, Hematology +15

Molecular characterization of β‐thalassemia mutations in Guadeloupe

Marc Romana, L. Kéclard, Gilles J. Guillemin et al. · American Journal of Hematology · 1996 · 23 citations

Life Sciences, Genetics, Molecular Genetics +14