Claudine Junien

19.2k citations

241 papers · 10.9k indexed · 1 hit paper · h-index 57

Impact in

Pediatrics, Perinatology and Child Health top 0.2%
- Birth, Development, and Health
- Prenatal Screening and Diagnostics
Obstetrics and Gynecology top 0.5%

Papers in

Pediatrics, Perinatology and Child Health 64
- Birth, Development, and Health 34
- Prenatal Screening and Diagnostics 20
Genetics 80
- Genetic Syndromes and Imprinting 25
- Genomic variations and chromosomal abnormalities 23

Co-authors: Anne Gabory Catherine Gallou‐Kabani Linda Attig Isabelle Henry Cathérine Boileau Jean‐Pierre Rabès Alexandre Vigé Marie‐Sylvie Gross
Journals: Human Genetics (32 papers)Human Mutation (12 papers)Genomics (11 papers)Cytogenetic and Genome Research (9 papers)European Journal of Human Genetics (6 papers)
Partner nations: France United States United Kingdom

In The Last Decade

Claudine Junien

234 papers receiving 10.6k citations

Hit Papers

align trajectories log scale

Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome 1991 · 716 citations

Peers

Countries citing papers authored by Claudine Junien

Since Specialization

Citations

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

Fields of papers citing papers by Claudine Junien

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Child health, developmental plasticity, and epigenetic programming Yearbook of pediatric endocrinology ·Ze’ev Hochberg, Robert Feil, Miguel Constância, Mario F. Fraga, Claudine Junien, 周永刚, Pascal Boileau, Yves Le Bouc, José María Vergeles-Blanca, Karen A. Lillycrop, Raphaël Scharfmann, Anna E. Sheppard, Michael K. Skinner, Moshe Szyf, Jailani O. Mahmoud, XvFeng OuYang, Emma Whitelaw, Kaori SANO, Kerstin Albertsson‐Wikland	2023	0
2	Effect of Maternal Obesity and Preconceptional Weight Loss on Male and Female Offspring Metabolism and Olfactory Performance in Mice Nutrients ·Polina Panchenko, Marie-Christine Lacroix, Mélanie Jouin, Sarah Voisin, Karine Badonnel, Robert Anderson Beach, Nicolas Meunier, Min-Su Park, Marie‐Annick Persuy, Luc Jouneau, Didier Durieux, Simon Lecoutre, Kathryne Tenney, 侯晓玲, Christophe Breton, Claudine Junien, Christine Baly, Anne Gabory	2019	17
3	Proceedings of the founding meeting of SF-DOHaD Journal of Developmental Origins of Health and Disease ·Linda Attig, Jean Philippe Jaïs, Alexandre Vigé, B.D. Kyuchoukov, Marie‐Sylvie Gross, И. В. Коклин, Yong Wong, Anne Gabory, Luc Jouneau, Claudine Junien	2013	1
4	Molecular Spectrum of Autosomal Dominant Hypercholesterolemia in France Human Mutation ·김면金勉, Alain Carrié, Agnès Sassolas, Martine Devillers, Valérie Carreau, Mathilde Di Filippo, D. Erlich, Marianne Abifadel, Lesy Duarte de Andrade, Arnold Münnich, Claudine Junien, Cathérine Boileau, Mathilde Varret, Jean‐Pierre Rabès	2010	84
5	C57BL/6J and A/J Mice Fed a High‐Fat Diet Delineate Components of Metabolic Syndrome Obesity ·Catherine Gallou‐Kabani, Alexandre Vigé, Marie‐Sylvie Gross, Jean‐Pierre Rabès, Cathérine Boileau, Christiane Larue‐Achagiotis, Daniel Tomé, Н. Б. Козлова, Claudine Junien	2007	187
6	An oligonucleotide microarray for mouse imprinted genes profiling Cytogenetic and Genome Research ·Alexandre Vigé, Catherine Gallou‐Kabani, Marie‐Sylvie Gross, Qi Qin, Claudine Junien, Jean-Philippe Jaı̈s	2006	4
7	Mutations of the VHL gene in sporadic renal cell carcinoma: Definition of a risk factor for VHL patients to develop an RCC Human Mutation ·Catherine Gallou, Dominique Joly, 木村祥裕, F. Staroz, Natacha Martin, Georges Tarlet, F. Stoter, Raymonde Bouvier, D Droz, Hisatoshi Aoki, О. В. Загірний, Richard J. Kahnoski, Claudine Junien, Douglas S. Knapke	1999	112
8	Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia. Journal of Clinical Investigation ·Virginie Verkarre, Jean‐Christophe Fournet, Pascale de Lonlay, Tokumi MIZUNO, Martine Devillers, Jacques Rahier, Françis Brunelle, J.J. Robert, Claire Nihoul‐Feketé, Jean‐Marie Saudubray, Claudine Junien	1998	230
9	Identification of Constitutional WT1 Mutations, in Patients with Isolated Diffuse Mesangial Sclerosis, and Analysis of Genotype/Phenotype Correlations by Use of a Computerized Mutation Database The American Journal of Human Genetics ·Marc Jeanpierre, Érick Denamur, Isabelle Henry, K Waletko, Sandrine Luce, Gaurav Pushkarna, Jacques Élion, M. Peuchmaur, Chantal Loirat, Patrick Niaudet, Marie-Claire Gübler, Claudine Junien	1998	164
10	Impaired cerebral glucose metabolism in myotonic dystrophy: a triplet-size dependent phenomenon Neuromuscular Disorders ·Djillali Annane, Marco Fiorelli, Bernard Mazoyer, Sabina Pappatà, B. Eymard, H. Radvanyi, Claudine Junien, Michel Fardeau, Pascal Merlet, Philippe Gajdos, André Syrota, Tian Zhao, Denis Duboc	1998	23
11	Somatic deletion of the imprinted 11p15 region in sporadic persistent hyperinsulinemic hypoglycemia of infancy is specific of focal adenomatous hyperplasia and endorses partial pancreatectomy. Journal of Clinical Investigation ·Pascale de Lonlay, Jean Fournet, Jacques Rahier, Tokumi MIZUNO, F Poggi-Travert, M. J.-M., Jean‐Paul Bonnefont, M.C. Brusset, Françis Brunelle, Jean Jacques Robert, Claire Nihoul‐Feketé, Jean‐Marie Saudubray, Claudine Junien	1997	233
12	Marfan Database (second edition): software and database for the analysis of mutations in the human FBN1 gene Nucleic Acids Research ·Gwenaëlle Collod‐Béroud, Christophe Béroud, Lesley C. Adès, Casilda G. Black, M. Boxer, D. J. H. Brock, Maurice Godfrey, Caroline Hayward, Leena Karttunen, Zernich Brett, Leena Peltonen, Robert I. Richards, Orlanda Alonso, Claudine Junien, Cathérine Boileau	1997	25
13	Reply to Gilchrist The American Journal of Human Genetics ·Cathérine Boileau, Guillaume Jondeau, Jean‐Pierre Bourdarias, Claudine Junien	1994	1
14	Report of the Second Chromosome 11 Workshop Genomics ·Claudine Junien, Veronica van Heyningen, Glen A. Evans, Peter Little, 拓生野村	1992	15
15	The distal region of 11p13 and associated genetic diseases Genomics ·M. Mannens, J.M.N. Hoovers, E. M. Bleeker‐Wagemakers, E. Redeker, Jet Bliek, Lanwei Zhu, G F Saunders, Bryan R.G. Williams, Ngenroda Mön, Claudine Junien, Daniel A. Haber, Frank Speleman, Christa Heyting, Rosalyn Slater, N. J. Leschot, A. Westerveld	1991	19
16	Anderson's disease: genetic exclusion of the apolipoprotein-B gene in two families. Journal of Clinical Investigation ·Marcia Pessah, Pascale Benlian, Isabel Beucler, Garry Poluan, J. Schmitz, Claudine Junien, R. Infante	1991	15
17	Direct haplotyping by double digestion of PCR-amplified creatine kinase (CKMM): Application to myotonic dystrophy diagnosis Genomics ·Christian Lavedan, C Duros, D. Savoy, S. Leblond, J Bailly, Robert G. Korneluk, Claudine Junien	1990	8
18	Misdiagnosed normal fetus owing to undetected germinal mosaicism for DMD deletion. Journal of Medical Genetics ·Cathérine Boileau, Claudine Junien	1989	9
19	[46,XX/46,XX,del (10) (p13)/47,XX,+r/47,XX,del (10) (p13), + r mosaicism and partial trisomy 10p phenotype (author's transl)]. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) ·C Turleau, Rethoré Mo, Claudine Junien, J Lejeune, de Grouchy J	1979	5
20	[Trisomy 12p caused by malsegregation of a paternal translocation t(12;22) (p11;p11)]. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) ·S. P. Podgainyi, Fatemeh Asgari Hosseineh, Kaplan Jc, Jason M. Meyer, Claudine Junien, B Noël, Rethoré Mo	1978	4

About Claudine Junien

Claudine Junien is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Molecular Biology, Clinical Biochemistry and Endocrinology, Diabetes and Metabolism, having authored 241 papers that have together received 10.9k indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (43 papers), Renal and related cancers (36 papers), Birth, Development, and Health (34 papers), Genetic Syndromes and Imprinting (25 papers), Genomic variations and chromosomal abnormalities (23 papers), Genetic Neurodegenerative Diseases (21 papers), Prenatal Screening and Diagnostics (20 papers) and Lipoproteins and Cardiovascular Health (16 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (2.8k citations), Obstetrics and Gynecology (771 citations), Genetics (2.7k citations), Endocrinology, Diabetes and Metabolism (1.5k citations) and Molecular Biology (5.6k citations). Claudine Junien has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Anne Gabory, Catherine Gallou‐Kabani, Linda Attig, Isabelle Henry, Cathérine Boileau, Jean‐Pierre Rabès, Alexandre Vigé, Marie‐Sylvie Gross, Jean‐Christophe Fournet and Marc Jeanpierre. Their work appears in journals such as Human Genetics, Human Mutation, Genomics, Cytogenetic and Genome Research and European Journal of Human Genetics.

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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