F. Barichard

409 total citations
12 papers, 311 citations indexed

About

F. Barichard is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, F. Barichard has authored 12 papers receiving a total of 311 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 4 papers in Pediatrics, Perinatology and Child Health and 4 papers in Genetics. Recurrent topics in F. Barichard's work include Renal and related cancers (5 papers), Epigenetics and DNA Methylation (4 papers) and Prenatal Screening and Diagnostics (4 papers). F. Barichard is often cited by papers focused on Renal and related cancers (5 papers), Epigenetics and DNA Methylation (4 papers) and Prenatal Screening and Diagnostics (4 papers). F. Barichard collaborates with scholars based in France, Canada and United Kingdom. F. Barichard's co-authors include Claudine Junien, Isabelle Henry, Marc Jeanpierre, P. Couillin, S Grandjouan, Thomas Gläser, Thierry Philip, J. L. Chaussain, Gilbert Lenoir and C Turleau and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Genomics and Human Genetics.

In The Last Decade

F. Barichard

12 papers receiving 308 citations

Peers

Countries citing papers authored by F. Barichard

Since Specialization

Citations

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

Fields of papers citing papers by F. Barichard

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of F. Barichard

This figure shows the co-authorship network connecting the top 25 collaborators of F. Barichard. A scholar is included among the top collaborators of F. Barichard 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 F. Barichard. F. Barichard is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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12 of 12 papers shown

#	Work	Indexed citations
1	Single base pair germ-line deletion in the p53 gene in a cancer predisposed family 1994 ·Human Genetics ·Richard C. Hamelin, F. Barichard, Isabelle Henry, Claudine Junien, Gilles Thomas	11
2	Pericentric intrachromosomal insertion responsible for recurrence of del(11)(p13p14) in a family 1993 ·Genes Chromosomes and Cancer ·Isabelle Henry, J.M.N. Hoovers, F. Barichard, (unknown), Anne Puech, Fabienne Prieur, Manfred Gessler, G.A.P. Bruns, Marcel M. A. M. Mannens, Claudine Junien	10
3	Molecular definition of de novo and genetically transmitted WAGR-associated rearrangements of 11p13 1989 ·Cytogenetic and Genome Research ·Christian Lavedan, F. Barichard, (unknown), P. Couillin, (unknown), (unknown), B Quack, M O Rethoré, B Noël, Claudine Junien	27
4	Mitotic deletions of 11p15.5 in two different tumors indicate that the CALCA locus is distal to the PTH locus 1989 ·Cytogenetic and Genome Research ·Isabelle Henry, S Grandjouan, F. Barichard, Marc Jeanpierre, Claudine Junien	4
5	Molecular definition of the 11p15.5 region involved in Beckwith-Wiedemann syndrome and probably in predisposition to adrenocortical carcinoma 1989 ·Human Genetics ·Isabelle Henry, Marc Jeanpierre, P. Couillin, F. Barichard, Jean‐Louis Serre, Hubert Journel, A. Lamouroux, C Turleau, J. de Grouchy, Claudine Junien	69
6	Characterization of a panel of somatic cell hybrids for subregional mapping along 11p and within band 11p13 1989 ·Human Genetics ·P. Couillin, (unknown), Isabelle Henry, N. Ravisé, (unknown), Marc Jeanpierre, F. Barichard, Philippe Métézeau, Jean‐Jacques Candelier, William H. Lewis, Veronica van Heyningen, Claudine Junien	18
7	Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinoma. 1989 ·Proceedings of the National Academy of Sciences ·Isabelle Henry, S Grandjouan, P. Couillin, F. Barichard, Marc Jeanpierre, Thomas Gläser, Thierry Philip, Gilbert Lenoir, J. L. Chaussain, Claudine Junien	119
8	Mapping of a human fibrillar collagen gene, pro α1(XI) (COL11A1), to the p21 region of chromosome 1 1988 ·Genomics ·Isabelle Henry, Alain Bernheim, Michael P. Bernard, Michel van der Rest, Tomoatsu Kimura, Marc Jeanpierre, F. Barichard, Roland Berger, Bjørn R. Olsen, Francesco Ramirez, Claudine Junien	17
9	Duplication of HRAS1, INS, and IGF2 is not a common event in Beckwith-Wiedemann syndrome. 1988 ·PubMed ·Isabelle Henry, Marc Jeanpierre, F. Barichard, (unknown), (unknown), C Turleau, de Grouchy J, Claudine Junien	9
10	Chromosomal assignment of the human 2,3-bisphosphoglycerate mutase gene (BPGM) to region 7q34→7q22 1987 ·Human Genetics ·F. Barichard, V. Joulin, Isabelle Henry, (unknown), (unknown), R Rosa, Michel Cohen‐Solal, Claudine Junien	14
11	The isolation, characterisation, and chromosomal assignment of the gene for human 3-hydroxy-3-methylglutaryl coenzyme A reductase, (HMG-CoA reductase) 1985 ·Human Genetics ·Steve E. Humphries, (unknown), Isabelle Henry, F. Barichard, Mikael Holm, Claudine Junien, R. Williamson	12
12	[Antenatal diagnosis of structural chromosome anomalies. 226 cases (author's transl)]. 1981 ·PubMed ·J Boué, F. Barichard, (unknown), (unknown), (unknown), A Boué	1

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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