Cécile Julier

15.2k total citations · 4 hit papers
109 papers, 11.3k citations indexed

About

Cécile Julier is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Cécile Julier has authored 109 papers receiving a total of 11.3k indexed citations (citations by other indexed papers that have themselves been cited), including 67 papers in Genetics, 42 papers in Molecular Biology and 39 papers in Surgery. Recurrent topics in Cécile Julier's work include Pancreatic function and diabetes (38 papers), Diabetes and associated disorders (33 papers) and Diabetes Management and Research (14 papers). Cécile Julier is often cited by papers focused on Pancreatic function and diabetes (38 papers), Diabetes and associated disorders (33 papers) and Diabetes Management and Research (14 papers). Cécile Julier collaborates with scholars based in France, United States and United Kingdom. Cécile Julier's co-authors include G.M. Lathrop, J.-M. Lalouel, J Ott, Jürg Ott, Marc Nicolino, Flemming Pociot, Jørn Nerup, Grant Morahan, Patrick Concannon and Stephen S. Rich and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

Cécile Julier

107 papers receiving 11.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Strategies for multilocus linkage analysis in humans.

1984 2.2k citations G.M. Lathrop, J.-M. Lalouel et al. profile →
Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes

2009 1.3k citations Patrick Concannon, Beena Akolkar et al. Nature Genetics profile →
Multilocus linkage analysis in humans: detection of linkage and estimation of recombination.

1985 1.0k citations G.M. Lathrop, J.-M. Lalouel et al. profile →
EIF2AK3, encoding translation initiation factor 2-α kinase 3, is mutated in patients with Wolcott-Rallison syndrome

2000 643 citations Marc Délepine, Marc Nicolino et al. Nature Genetics profile →

Peers

Countries citing papers authored by Cécile Julier

Since Specialization

Citations

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

Fields of papers citing papers by Cécile Julier

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cécile Julier

This figure shows the co-authorship network connecting the top 25 collaborators of Cécile Julier. A scholar is included among the top collaborators of Cécile Julier based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Cécile Julier. Cécile Julier is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	tRNA Methyltransferase Homolog Gene TRMT10A Mutation in Young Onset Diabetes and Primary Microcephaly in Humans 2013 ·PLoS Genetics ·Mariana Igoillo‐Esteve, (unknown), Nelle Lambert, Julie Désir, Isabelle Pirson, Baroj Abdulkarim, Nicolas Simonis, (unknown), Lorella Marselli, Piero Marchetti, Pierre Vanderhaeghen, Décio L. Eizirik, Wim Wuyts, Cécile Julier, Ali Chakera, Sian Ellard, Andrew T. Hattersley, Marc Abramowicz, Miriam Cnop	95
2	Confirmation of novel type 1 diabetes risk loci in families 2012 ·Diabetologia ·Jason D. Cooper, Joanna M. M. Howson, (unknown), Neil Walker, Helen Stevens, Jennie H. M. Yang, Jin‐Xiong She, George S. Eisenbarth, Marian Rewers, John A. Todd, Beena Akolkar, Patrick Concannon, (unknown), Cécile Julier, Grant Morahan, Jørn Nerup, Concepcion R. Nierras, Flemming Pociot, Stephen S. Rich	43
3	Tests for Genetic Interactions in Type 1 Diabetes 2011 ·Diabetes ·Grant Morahan, Munish Mehta, Ian James, Wei‐Min Chen, Beena Akolkar, (unknown), Joan E. Hilner, Cécile Julier, Jørn Nerup, Concepcion R. Nierras, Flemming Pociot, John A. Todd, Stephen S. Rich	36
4	Evidence for association of the TCF7 locus with type I diabetes 2009 ·Genes and Immunity ·(unknown), Ana M. Valdes, Cécile Julier, Daniel B. Mirel, Janelle A. Noble	25
5	Overview of the Type I Diabetes Genetics Consortium 2009 ·Genes and Immunity ·Stephen S. Rich, Beena Akolkar, Patrick Concannon, (unknown), Joan E. Hilner, Cécile Julier, Grant Morahan, Jørn Nerup, Concepcion R. Nierras, Flemming Pociot, John A. Todd	49
6	Correction: Genetic Determination and Linkage Mapping of Plasmodium falciparum Malaria Related Traits in Senegal 2008 ·PLoS ONE ·Anavaj Sakuntabhai, (unknown), Isabelle Casadémont, Chayanon Peerapittayamongkol, Christophe Rogier, Patricia Tortevoye, Adama Tall, Richard J. Paul, Chairat Turbpaiboon, (unknown), Jean‐François Trape, André Spiegel, Simon Heath, Odile Mercereau‐Puijalon, Alioune Dièye, Cécile Julier	4
7	Mutations in GLIS3 are responsible for a rare syndrome with neonatal diabetes mellitus and congenital hypothyroidism 2006 ·Nature Genetics ·Valérie Senée, Claude Chelala, Sabine Duchatelet, Daorong Feng, Hervé Blanc, Jack‐Christophe Cossec, Céline Charon, Marc Nicolino, Pascal Boileau, Douglas R. Cavener, Pierre Bougnères, Doris Taha, Cécile Julier	270
8	Linkage mapping for hypertension susceptibility genes 1999 ·Current Hypertension Reports ·Norihiro Kato, Cécile Julier	9
9	Comparative mapping of novel simple sequence repeat markers in a hypertension-related region on rat chromosome 1 1997 ·Mammalian Genome ·Toru Nabika, (unknown), Kazuhiro Kitada, Tadao Serikawa, Tomoji Mashimo, Florent Soubrier, Cécile Julier, Yoichi Ohno, Takao Saruta, Hisao Tanase, Junichi Masuda, Yukio Yamori, Yasuo Nara	17
10	Genetic Susceptibility for Human Familial Essential Hypertension in a Region of Homology with Blood Pressure Linkage on Rat Chromosome 10 1997 ·Human Molecular Genetics ·Cécile Julier, Marc Délepine, Bernard Keavney, Joseph D. Terwilliger, Sean Davis, Daniel E. Weeks, Thuỳ Anh Bùi, Xavier Jeunemaı̂tre, Gilberto Velho, Philippe Froguel, Peter J. Ratcliffe, Pierre Corvol, Florent Soubrier, G. Mark Lathrop	139
11	Génotypes HLA-DR:DQ et diabète insulino-dépendant en milieu sénégalais. 1996 ·(unknown), (unknown), Cécile Julier, Didier Chevenne, (unknown), F Trivin, (unknown), (unknown), (unknown)	1
12	Contribution of genes of the major histocompatibility complex to susceptibility and disease phenotype in inflammatory bowel disease 1996 ·The Lancet ·(unknown), J. Mark Farrant, (unknown), J I Bell, (unknown), Michael Bunce, Cécile Julier	268
13	Distribution of HLA‐DQA1 and ‐DQB1 alleles and DQA1‐DQB1 genotypes among Senegalese patients with insulin‐dependent diabetes mellitus 1996 ·Tissue Antigens ·(unknown), (unknown), Didier Chevenne, Béatrice Parfait, Cécile Julier, (unknown), (unknown), F Trivin	7
14	Regulation of insulin gene expression by the IDDM associated, insulin locus haplotype 1995 ·Human Molecular Genetics ·Anneke Lucassen, Gavin Screaton, Cécile Julier, Tim Elliott, Mark Lathrop, (unknown)	82
15	Linkage analysis in juvenile neuronal ceroid lipofuscinosis 1992 ·American Journal of Medical Genetics ·Jonathan L. Haines, (unknown), Rose‐Mary Boustany, Ann Jewell, Cécile Julier, Xandra O. Breakefield, James F. Gusella	9
16	Human Variable Number of Tandem Repeat Probes As a Source of Polymorphic Markers in Experimental Animals 1991 ·Proceedings of the Fourth International Symposium on Polarization Phenomena in Nuclear Reactions ·Béatrice Gouyon, Cécile Julier, Philip Avner, Michel Georges, Mark Lathrop	3
17	A primary map of 24 loci on human chromosome 16 1990 ·Genomics ·Cécile Julier, Yusuke Nakamura, Mark Lathrop, P. O’Connell, Mark Leppert, T. Mohandas, Jean‐Marc Lalouel, R. White	41
18	Isolation and mapping of a polymorphic DNA sequence (HBI18P1) on chromosome 11 [D11S147] 1989 ·Nucleic Acids Research ·Cécile Julier, Yusuke Nakamura, G.M. Lathrop, J.-M. Lalouel, R. White	2
19	Isolation and mapping of a polymorphic DNA sequence (CJ52.1) on chromosome 16 [D16S152] 1989 ·Nucleic Acids Research ·Cécile Julier, Yusuke Nakamura, G.M. Lathrop, J.-M. Lalouel, R. White	1
20	Isolation and mapping of a polymorphic DNA sequence (CJ52.193) on chromosome 11 [D11S384] 1989 ·Nucleic Acids Research ·Cécile Julier, (unknown), Yusuke Nakamura, G.M. Lathrop, J.-M. Lalouel, R. White	3

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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