Jacques Loiselet

4.3k citations

60 papers · 2.6k indexed · h-index 25

Impact in

Sensory Systems top 0.5%
- Hearing, Cochlea, Tinnitus, Genetics
Neurology top 5%
- Vestibular and auditory disorders

Papers in

Sensory Systems 9
- Hearing, Cochlea, Tinnitus, Genetics 9
Anatomy 1

Co-authors: Marie‐Paule Lefranc Nabiha Salem Mirna Mustapha André Mégarbané Christine Petit Elie El‐Zir Shin’ichiro Yasunaga Martine Cohen‐Salmon
Journals: European Journal of Human Genetics (7 papers)Human Genetics (5 papers)European Journal of Medical Genetics (2 papers)The American Journal of Human Genetics (2 papers)Clinical Genetics (2 papers)
Partner nations: Lebanon France United States

In The Last Decade

Jacques Loiselet

60 papers receiving 2.5k citations

Peers

Countries citing papers authored by Jacques Loiselet

Since Specialization

Citations

This map shows the geographic impact of Jacques Loiselet's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Jacques Loiselet with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jacques Loiselet more than expected).

Fields of papers citing papers by Jacques Loiselet

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jacques Loiselet. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Jacques Loiselet. The network helps show where Jacques Loiselet may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Jacques Loiselet, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Jacques Loiselet Line = papers co-authored together Jacques Loiselet links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Familial Mediterranean fever (FMF) in Lebanon and Jordan: a population genetics study and report of three novel mutations European Journal of Medical Genetics ·Myrna Medlej‐Hashim, Jean‐Louis Serre, Sandra Corbani, Tarquino Saltos, Nadine Jalkh, Valérie Delague, Éliane Chouery, Nabiha Salem, Jacques Loiselet, Marie‐Paule Lefranc, André Mégarbané	2005	46
2	La fièvre méditerranéenne familiale (FMF) : du diagnostic au traitement Cahiers d'études et de recherches francophones / Santé ·Myrna Medlej‐Hashim, Jacques Loiselet, Marie‐Paule Lefranc, André Mégarbané	2004	1
3	Amyloidosis in familial Mediterranean fever patients: correlation with MEFV genotype and SAA1 and MICA polymorphisms effects BMC Medical Genetics ·Myrna Medlej‐Hashim, Valérie Delague, Éliane Chouery, Nabiha Salem, M. O. Rawashdeh, Marie‐Paule Lefranc, Jacques Loiselet, André Mégarbané	2004	51
4	Molecular characterization of G6PD deficiency in Cyprus Blood Cells Molecules and Diseases ·Anthi Drousiotou, S. B. Kargbo, Qiongyao Ruan, Jacques Loiselet, Г И Гольдгамер, Brian C. Verrelli, Sarah A. Tishkoff	2004	22
5	A new dominant branchiogenic‐deafness syndrome with internal auditory canal hypoplasia and abnormal extremities American Journal of Medical Genetics Part A ·André Mégarbané, Yi‐Cheng Hou, Éliane Chouery, Valérie Delague, Gustavo Pérez de Nanclares, 糺真鍋, Luís Castaño, Jacques Loiselet	2003	2
6	Non-syndromic recessive deafness in Jordan: mapping of a new locus to chromosome 9q34.3 and prevalence of DFNB1 mutations European Journal of Human Genetics ·Myrna Medlej‐Hashim, Mirna Mustapha, Éliane Chouery, Dominique Weil, Durdane Ozturk, Nabiha Salem, Valérie Delague, Jacques Loiselet, Mark Lathrop, Christine Petit, André Mégarbané	2002	25
7	Evidence for Balancing Selection from Nucleotide Sequence Analyses of Human G6PD The American Journal of Human Genetics ·Brian C. Verrelli, John H. McDonald, George Argyropoulos, Giovanni Destro‐Bisol, Alain Froment, Anthi Drousiotou, Marie‐Paule Lefranc, Ahmed Noureddine Helal, Jacques Loiselet, Sarah A. Tishkoff	2002	119
8	DFNB31, a recessive form of sensorineural hearing loss, maps to chromosome 9q32-34 European Journal of Human Genetics ·Mirna Mustapha, Éliane Chouery, Sébastien Chardenoux, Ooi Kee Beng, Joël Paronnaud, Arnaud Lemainque, André Mégarbané, Jacques Loiselet, Dominique Weil, Mark Lathrop, Christine Petit	2002	28
9	A new autosomal recessive non-progressive congenital cerebellar ataxia associated with mental retardation, optic atrophy, and skin abnormalities (CAMOS) maps to chromosome 15q24-q26 in a large consanguineous Lebanese Druze family Neurogenetics ·Valérie Delague, Corinne Bareil, Patrice Bouvagnet, Nabiha Salem, Éliane Chouery, Jacques Loiselet, André Mégarbané, Mireille Claustres	2002	17
10	Genetic screening of fourteen mutations in Jordanian familial Mediterranean fever patients Human Mutation ·Myrna Medlej‐Hashim, M. O. Rawashdeh, Éliane Chouery, Issam Mansour, Valérie Delague, Marie‐Paule Lefranc, Roger Naman, Jacques Loiselet, Leann Anderson	2000	51
11	Mapping of a New Locus for Autosomal Recessive Demyelinating Charcot-Marie-Tooth Disease to 19q13.1-13.3 in a Large Consanguineous Lebanese Family: Exclusion of MAG as a Candidate Gene The American Journal of Human Genetics ·Valérie Delague, Corinne Bareil, Sylvie Tuffery‐Giraud, Patrice Bouvagnet, Éliane Chouery, Salam Koussa, Thierry Maisonobe, Jacques Loiselet, André Mégarbané, Mireille Claustres	2000	64
12	Mutational Analysis in Lebanese Patients with Congenital Adrenal Hyperplasia due to a Deficit in 21-Hydroxylase Hormone Research in Paediatrics ·Valérie Delague, Erik van Zwet, Eliane Khallouf, Véronique Tardy, Éliane Chouery, Georges Halaby, Jacques Loiselet, Yves Morel, André Mégarbané	2000	11
13	Exclusion of chromosome 15q21.1 in autosomal‐recessive Weill–Marchesani syndrome in an inbred Lebanese family Clinical Genetics ·André Mégarbané, Mirna Mustapha, Jamal Bleik, Dragan Nastev, Valérie Delague, Jacques Loiselet	2000	9
14	A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness Nature Genetics ·Shin’ichiro Yasunaga, M’hamed Grati, Martine Cohen‐Salmon, A. Amraoui, Mirna Mustapha, Nabiha Salem, Elie El‐Zir, Jacques Loiselet, Christine Petit	1999	429
15	Calpain 3 deficiency is associated with myonuclear apoptosis and profound perturbation of the IκBα/NF-κB pathway in limb-girdle muscular dystrophy type 2A Nature Medicine ·Stephen Baghdiguian, Marianne Martin, Isabelle Richard, Françoise Pons, Catherine Astier, Nathalie Bourg, Ronald T. Hay, Atharv Rajesh Gangodkar, Georges Halaby, Jacques Loiselet, Louise V.B. Anderson, Adolfo López de Munaín, Michel Fardeau, Paul Mangeat, J. Beckmann, Marie‐Paule Lefranc	1999	240
16	Identification of a locus on chromosome 7q31, DFNB14, responsible for prelingual sensorineural non-syndromic deafness European Journal of Human Genetics ·Mirna Mustapha, Nabiha Salem, Dominique Weil, Elie El‐Zir, Jacques Loiselet, Christine Petit	1998	16
17	A sensorineural progressive autosomal recessive form of isolated deafness, DFNB13, maps to chromosome 7q34-q36 European Journal of Human Genetics ·Mirna Mustapha, Sébastien Chardenoux, Pananee Phueksuwan, Nabiha Salem, Jean Weissenbach, Elie El‐Zir, Jacques Loiselet, Christine Petit	1998	29
18	Clinical manifestation of a severe neonatal progeroid syndrome Clinical Genetics ·André Mégarbané, Jacques Loiselet	1997	5
19	Cystic fibrosis in Lebanon: distribution of CFTR mutations among Arab communities Human Genetics ·Marie Desgeorges, André Mégarbané, Caroline Guittard, 马红芳, Jacques Loiselet, Jacques Demaille, Mireille Claustres	1997	51
20	[ON GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY IN AUTOCHTHONOUS POPULATIONS OF LEBANON]. PubMed ·Chenyang Cui, Jacques Loiselet, Natsuki Shikida, Septiani Septiani	1964	7

About Jacques Loiselet

Jacques Loiselet is a scholar working on Sensory Systems, Anatomy, Genetics, Immunology and Clinical Biochemistry, having authored 60 papers that have together received 2.6k indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (9 papers), Inflammasome and immune disorders (8 papers), Neonatal Health and Biochemistry (6 papers), Immune Cell Function and Interaction (5 papers), interferon and immune responses (4 papers), Metabolism and Genetic Disorders (4 papers), Connexins and lens biology (4 papers) and Hemoglobinopathies and Related Disorders (4 papers). The work is most often cited by research in Sensory Systems (547 citations), Neurology (251 citations), Cell Biology (373 citations), Molecular Biology (1.3k citations) and Genetics (490 citations). Jacques Loiselet has collaborated with scholars based in Lebanon, France and United States. Frequent co-authors include Marie‐Paule Lefranc, Nabiha Salem, Mirna Mustapha, André Mégarbané, Christine Petit, Elie El‐Zir, Shin’ichiro Yasunaga, Martine Cohen‐Salmon, M’hamed Grati and A. Amraoui. Their work appears in journals such as European Journal of Human Genetics, Human Genetics, European Journal of Medical Genetics, The American Journal of Human Genetics and Clinical Genetics.

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