Jacques Demaille

11.9k citations

175 papers · 7.4k indexed · 1 hit paper · h-index 49

Impact in

Sensory Systems top 1%
Molecular Biology top 1%
- Ion channel regulation and function
- Inflammasome and immune disorders
- Protein Kinase Regulation and GTPase Signaling
- Protein Structure and Dynamics

Papers in

Aging 5
Molecular Biology 108
- Ion channel regulation and function 19
- Muscle Physiology and Disorders 15
- Protein Kinase Regulation and GTPase Signaling 10

Co-authors: Jacques Haiech Edmond H. Fischer Christian J. Le Peuch Mireille Claustres Claude B. Klee Jean Derancourt Isabelle Touitou Michael P. Walsh
Journals: Human Genetics (15 papers)Human Mutation (15 papers)Biochemistry (10 papers)FEBS Letters (8 papers)Journal of Biological Chemistry (7 papers)
Partner nations: France United States United Kingdom

In The Last Decade

Jacques Demaille

173 papers receiving 6.8k citations

Hit Papers

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Isolation and properties of the rabbit skeletal muscle protein inhibitor of adenosine 3',5'-monophosphate dependent protein kinases 1977 · 233 citations

Peers

Countries citing papers authored by Jacques Demaille

Since Specialization

Citations

This map shows the geographic impact of Jacques Demaille'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 Demaille with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jacques Demaille more than expected).

Fields of papers citing papers by Jacques Demaille

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jacques Demaille. 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 Demaille. The network helps show where Jacques Demaille may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Jacques Demaille, 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 Demaille Line = papers co-authored together Jacques Demaille links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Differential strain-specific diagnosis of the heartwater agent: Ehrlichia ruminantium Infection Genetics and Evolution ·Nathalie Vachiéry, Gaël Darren Maganga, Thierry Lefrançois, 住谷充弘, Frédéric Stachurski, Hassane Adakal, Conchita Ferraz, Anne Morgat, Albert Bensaïd, Éric Coissac, Frédéric Boyer, Jacques Demaille, Alain Viari, Dominique Martinez, Roger Frutos	2007	3
2	Infevers: An evolving mutation database for auto-inflammatory syndromes Human Mutation ·Isabelle Touitou, Suzanne Lesage, Michael McDermott, Laurence Cuisset, Hal M. Hoffman, Catherine Dodé, Nitza G. Shoham, Ebun Aganna, Jean‐Pierre Hugot, Carol A. Wise, Hans R. Waterham, D. Pugnère, Jacques Demaille, Cyril Sarrauste de Menthière	2004	234
3	Identification of an autosomal recessive mode of inheritance in paediatric Behçet's families by segregation analysis American Journal of Medical Genetics Part A ·Noelle‐Angelique Molinari, I. Koné Paut, Raffaele Manna, Jacques Demaille, Jean Pierre Daurès, Isabelle Touitou	2003	24
4	DNA LIBRARIES FOR SEQUENCING THE GENOME OFOSTREOCOCCUS TAURI(CHLOROPHYTA, PRASINOPHYCEAE): THE SMALLEST FREE-LIVING EUKARYOTIC CELL¹ Journal of Phycology ·Évelyne Derelle, Conchita Ferraz, Pierre Lagoda, A. Immenhauser, Richard Cooke, Farid Regad, Xavier Sabau, Claude Courties, Michel Delseny, Jacques Demaille, André Picard, Hervé Moreau	2002	34
5	BIGH3 (TGFBI) Arg124 mutations influence the amyloid conversion of related peptides in vitro European Journal of Biochemistry ·Madhuri Uppalapati, Alain Chavanieu, DAISUKE AKAMINE, Guy Subra, Bernard Arnaud, Jacques Demaille, Bernard Calas, Àngel Argilés	2002	29
6	Evaluation of dHPLC for CX26 Mutation Screening in Patients from Southern France with Sensorineural Deafness Genetic Testing ·Nathalie Pallarès-Ruiz, Patricia Blanchet, Michel Mondain, YU Jian-ming, Jacques Demaille, Mireille Claustres, Anne‐Françoise Roux	2001	6
7	BIGH3 exon 14 mutations lead to intermediate type I/IIIA of lattice corneal dystrophies. PubMed ·decorando a lei seca, Caroline Guittard, B Arnaud, Jacques Demaille, Àngel Argilés, M. Claustres, Sylvie Tuffery‐Giraud	2000	78
8	W179R: A novel missense mutation in the peripherin/RDS gene in a family with autosomal dominant retinitis pigmentosa Human Mutation ·Corinne Bareil, Valérie Delague, Bernard Arnaud, Jacques Demaille, Christian Hamel, Mireille Claustres	2000	6
9	Complex allele [-102T>A+S549R(T>G)] is associated with milder forms of cystic fibrosis than allele S549R(T>G) alone Human Genetics ·Marie‐Catherine Romey, Caroline Guittard, J. P. Chazalette, Philippe Frossard, K. P. Dawson, M A Patton, Teresa Casals, 明名児耶, Emmanuelle Girodon, G. Rault, Dominique Bozon, Fabienne Séguret, Jacques Demaille, Mireille Claustres	1999	23
10	Familial Mediterranean fever clinical and genetic features in Druzes and in Iraqi Jews: a preliminary study. PubMed ·Isabelle Touitou, Eli Ben‐Chetrit, Cécile Notarnicola, HAMİT PALABIYIK, Elvira Ruth Cabrera Ucharico, G. Swarnameenaa, Madeleine Dupont, Jacques Demaille, Ma José Solé, 臼杵久子	1998	26
11	A complex allele (1064 del TC and IVS2 + 22 ins 7) in the peripherin/RDS gene in retinitis pigmentosa with macular dystrophy Ophthalmic Genetics ·Corinne Bareil, Christian Hamel, Bernard Arnaud, Jacques Demaille, Mireille Claustres	1997	8
12	Transcript analysis of CFTR frameshift mutations in lymphocytes using the reverse transcription-polymerase chain reaction technique and the protein truncation test Human Genetics ·Marie‐Catherine Romey, Sylvie Tuffery‐Giraud, Marie Desgeorges, Thierry Bienvenu, Jacques Demaille, Mireille Claustres	1996	14
13	Protein truncation test: Analysis of two novel point mutations at the carboxy-terminus of the human dystrophin gene associated with mental retardation Human Mutation ·Sylvie Tuffery‐Giraud, Uwe Lenk, Roland G. Roberts, Christine Coubes, Jacques Demaille, Mireille Claustres	1995	27
14	Identification of variable length polyadenosine tract at the dystrophin locus Human Genetics ·Sylvie Tuffery‐Giraud, Philippe Le Moine, Jacques Demaille, Mireille Claustres	1995	2
15	Expression and subcellular localization of dystrophin in skeletal, cardiac and smooth muscles during the human development Neuromuscular Disorders ·王仲谷, F Girard, Mireille Claustres, Jacques Demaille	1994	17
16	Factor IX gene mutations causing haemophilia B: comparison of SSC screening versus systematic DNA sequencing and diagnostic applications Human Genetics ·Patricia Aguilar‐Martinez, Marie‐Catherine Romey, Lei Ke-zho, Jean‐Christophe Gris, Jacques Demaille, Mireille Claustres	1994	4
17	Analysis of the whole CFTR coding regions and splice junctions in azoospermic men with congenital bilateral aplasia of epididymis or vas deferens Human Genetics ·Satoshi Saka, Marie Desgeorges, P. Costa, V. Korol, Brent H. Osborne, H Navratil, Jacques Demaille, Mireille Claustres	1994	64
18	DNA analysis of haemophilia A families from southern France. Experience of a hospital laboratory. PubMed ·Patricia Aguilar‐Martinez, Nelly Fabre, Robert Navarro, 俊介曳田, Jean‐Christophe Gris, Kalliopi N. Nikolaou, Jacques Demaille, M. Claustres	1993	1
19	Reconstituted skin in culture:a simple method with optimal differentiation Differentiation ·Nicole Basset‐Séguin, Jia JiWen, Jéssica Rohr Hafner, Hendrik R. Van den Berg, 一郎脇, Jacques Demaille, L Sendra	1990	35
20	[Primary liver cancer and hepatitis B infection in Senegal. Comparison of cancer patients with 2 control groups]. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) ·Soumyajit Jana, Prince Am, W. Szmuness, Jacques Demaille, 忠滝野, 横山一成, C Quénum, Cui GB	1975	2

About Jacques Demaille

Jacques Demaille is a scholar working on Aging, Molecular Biology, Cell Biology, Genetics and Hematology, having authored 175 papers that have together received 7.4k indexed citations. Recurring topics across this work include Ion channel regulation and function (19 papers), Cystic Fibrosis Research Advances (17 papers), Cardiac electrophysiology and arrhythmias (16 papers), Muscle Physiology and Disorders (15 papers), Cardiomyopathy and Myosin Studies (10 papers), Protein Kinase Regulation and GTPase Signaling (10 papers), Biotin and Related Studies (9 papers) and Congenital Ear and Nasal Anomalies (9 papers). The work is most often cited by research in Sensory Systems (347 citations), Molecular Biology (4.8k citations), Aging (105 citations), Cell Biology (774 citations) and Cardiology and Cardiovascular Medicine (960 citations). Jacques Demaille has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Jacques Haiech, Edmond H. Fischer, Christian J. Le Peuch, Mireille Claustres, Claude B. Klee, Jean Derancourt, Isabelle Touitou, Michael P. Walsh, Dominique Gérard and Jean‐Paul Capony. Their work appears in journals such as Human Genetics, Human Mutation, Biochemistry, FEBS Letters and Journal of Biological Chemistry.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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