Laurence Taine

2.3k total citations
46 papers, 924 citations indexed

About

Laurence Taine is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Laurence Taine has authored 46 papers receiving a total of 924 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 21 papers in Genetics and 14 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Laurence Taine's work include Genomic variations and chromosomal abnormalities (14 papers), Prenatal Screening and Diagnostics (9 papers) and Porphyrin Metabolism and Disorders (6 papers). Laurence Taine is often cited by papers focused on Genomic variations and chromosomal abnormalities (14 papers), Prenatal Screening and Diagnostics (9 papers) and Porphyrin Metabolism and Disorders (6 papers). Laurence Taine collaborates with scholars based in France, Spain and United Kingdom. Laurence Taine's co-authors include Robert Saura, Didier Lacombe, Hubert de Verneuil, François Moreau‐Gaudry, J. Horovitz, Benoı̂t Arveiler, B. Maugey‐Laulom, Denis Roux, Frédéric Mazurier and Antonio Fontanellas and has published in prestigious journals such as Hepatology, The American Journal of Human Genetics and The American Journal of Surgical Pathology.

In The Last Decade

Laurence Taine

46 papers receiving 856 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Laurence Taine France	21	428	398	274	147	86	46	924
Sevim Balcı Türkiye	17	552 1.3×	463 1.2×	181 0.7×	200 1.4×	160 1.9×	70	1.2k
Walter Fuhrmann Germany	17	259 0.6×	424 1.1×	261 1.0×	160 1.1×	66 0.8×	86	898
Nicolette S. den Hollander Netherlands	21	510 1.2×	499 1.3×	409 1.5×	183 1.2×	23 0.3×	43	1.6k
Isabel Lorda‐Sánchez Spain	23	558 1.3×	759 1.9×	689 2.5×	130 0.9×	28 0.3×	67	1.4k
Joy D.A. Delhanty United Kingdom	17	267 0.6×	290 0.7×	423 1.5×	128 0.9×	17 0.2×	30	796
Peter Miny Germany	21	437 1.0×	629 1.6×	844 3.1×	203 1.4×	26 0.3×	88	1.5k
K Imaizumi Japan	15	566 1.3×	404 1.0×	88 0.3×	143 1.0×	89 1.0×	27	885
Christine Oley United Kingdom	13	572 1.3×	431 1.1×	192 0.7×	76 0.5×	19 0.2×	21	954
Atsuko Fujimoto United States	19	310 0.7×	489 1.2×	267 1.0×	111 0.8×	26 0.3×	45	868
Amber N. Pursley United States	20	498 1.2×	1.1k 2.8×	690 2.5×	61 0.4×	32 0.4×	28	1.4k

Countries citing papers authored by Laurence Taine

Since Specialization

Citations

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

Fields of papers citing papers by Laurence Taine

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laurence Taine

This figure shows the co-authorship network connecting the top 25 collaborators of Laurence Taine. A scholar is included among the top collaborators of Laurence Taine 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 Laurence Taine. Laurence Taine 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

Van‐Gils, Julien, Sophie Naudion, Jérôme Toutain, et al.. (2019). Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP mutations. Clinical Genetics. 95(3). 420–426. 8 indexed citations

Toutain, Jérôme, et al.. (2012). Proportion of Parents Agreeing to Delay Fetal Karyotyping until the Third Trimester of Pregnancy in Cases with an Indication. Fetal Diagnosis and Therapy. 31(2). 115–121. 1 indexed citations

Toutain, Jérôme, Laurence Taine, Fanny Morice‐Picard, et al.. (2011). An unusual chromosome 22q11 deletion associated with an apparent complementary ring chromosome in a phenotypically normal woman. European Journal of Medical Genetics. 54(3). 292–294. 1 indexed citations

Lüdecke, Hermann‐Josef, Igor Sibon, Christophe Richez, et al.. (2011). Rheumatologic and neurological events in an elderly patient with tricho-rhino-phalangeal syndrome type I. European Journal of Medical Genetics. 54(4). e405–e408. 6 indexed citations

Richard, Élodie, François Moreau‐Gaudry, Magalie Lalanne, et al.. (2008). Effective Gene Therapy of Mice with Congenital Erythropoietic Porphyria Is Facilitated by a Survival Advantage of Corrected Erythroid Cells. The American Journal of Human Genetics. 82(1). 113–124. 37 indexed citations

Schneider, Anouck, Brigitte Benzacken, Agnès Guichet, et al.. (2008). Molecular cytogenetic characterization of terminal 14q32 deletions in two children with an abnormal phenotype and corpus callosum hypoplasia. European Journal of Human Genetics. 16(6). 680–687. 21 indexed citations

Brémond‐Gignac, Dominique, John A. Crolla, Henri Copin, et al.. (2005). Combination of WAGR and Potocki–Shaffer contiguous deletion syndromes in a patient with an 11p11.2–p14 deletion. European Journal of Human Genetics. 13(4). 409–413. 32 indexed citations

Brun, J.-L., Flore Gangbo, Laurence Taine, et al.. (2004). Prenatal diagnosis and management of sex chromosome aneuploidy: a report on 98 cases. Prenatal Diagnosis. 24(3). 213–218. 51 indexed citations

Goizet, Cyril, Isabelle Coupry, Caroline Rooryck, et al.. (2004). Molecular characterization of an 11q14.3 microdeletion associated with leukodystrophy. European Journal of Human Genetics. 12(3). 245–250. 9 indexed citations

10.

Vergier, B., Marc‐Antoine Belaud‐Rotureau, Marie‐Noëlle Benassy, et al.. (2004). Neoplastic Cells Do Not Carry bcl2-JH Rearrangements Detected in a Subset of Primary Cutaneous Follicle Center B-cell Lymphomas. The American Journal of Surgical Pathology. 28(6). 748–755. 23 indexed citations

11.

Brun, J.-L., Flore Gangbo, Frédéric Guyon, et al.. (2003). Feasibility, accuracy and safety of chorionic villus sampling: a report of 10 741 cases. Prenatal Diagnosis. 23(4). 295–301. 43 indexed citations

12.

Fontanellas, Antonio, Manuel Méndez, Frédéric Mazurier, et al.. (2001). Successful therapeutic effect in a mouse model of erythropoietic protoporphyria by partial genetic correction and fluorescence-based selection of hematopoietic cells. Gene Therapy. 8(8). 618–626. 22 indexed citations

13.

Richard, Emmanuel, Manuel Méndez, Frédéric Mazurier, et al.. (2001). Gene Therapy of a Mouse Model of Protoporphyria with a Self-Inactivating Erythroid-Specific Lentiviral Vector without Preselection. Molecular Therapy. 4(4). 331–338. 49 indexed citations

14.

Guyon, Frédéric, Laurence Taine, Denis Roux, et al.. (2001). Pregnancy Outcome and Prognosisin Fetuses with Increased First-TrimesterNuchal Translucency. Fetal Diagnosis and Therapy. 16(6). 360–363. 32 indexed citations

15.

Dupuy, Denis, Incarnation Aubert, Véronique Guyonnet Dupérat, et al.. (2000). Mapping, Characterization, and Expression Analysis of the SM-20 Human Homologue, C1orf12, and Identification of a Novel Related Gene, SCAND2. Genomics. 69(3). 348–354. 32 indexed citations

16.

Frengen, Eirik, Philippe Rocca‐Serra, Sergey Shaposhnikov, et al.. (2000). High-Resolution Integrated Map Encompassing the Breast Cancer Loss of Heterozygosity Region on Human Chromosome 16q22.1. Genomics. 70(3). 273–285. 12 indexed citations

17.

Mazurier, Frédéric, Antonio Fontanellas, Stéphanie Salesse, et al.. (1999). A Novel Immunodeficient Mouse Model-RAG2 gamma Cytokine Receptor Chain Double Mutants-Requiring Exogenous Cytokine Administration for Human Hematopoietic Stem Cell Engraftment Common. Journal of Interferon & Cytokine Research. 19(5). 533–541. 94 indexed citations

18.

Biancalana, Valérie, Laurence Taine, J. Bouix, et al.. (1996). Expansion and methylation status at FRAXE can be detected on EcoRI blots used for FRAXA diagnosis: analysis of four FRAXE families with mild mental retardation in males.. PubMed. 59(4). 847–54. 24 indexed citations

19.

Ged, Cécile, François Moreau‐Gaudry, Laurence Taine, et al.. (1996). PRENATAL DIAGNOSIS IN CONGENITAL ERYTHROPOIETIC PORPHYRIA BY METABOLIC MEASUREMENT AND DNA MUTATION ANALYSIS. Prenatal Diagnosis. 16(1). 83–86. 22 indexed citations

20.

Longy, Michel, et al.. (1993). Chromosome analysis of adenomatous polyps of the colon. Cancer Genetics and Cytogenetics. 67(1). 7–13. 25 indexed citations

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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