Laurence Taine

2.3k citations

46 papers · 924 indexed · h-index 21

Developmental Biology top 5%
- Congenital limb and hand anomalies 5
Genetics top 5%
- Genomic variations and chromosomal abnormalities 14
- Genetics and Neurodevelopmental Disorders 5
- Virus-based gene therapy research 3
Pediatrics, Perinatology and Child Health top 5%
- Prenatal Screening and Diagnostics 9
Molecular Biology
- Porphyrin Metabolism and Disorders 6
- RNA modifications and cancer 6
Pathology and Forensic Medicine
Surgery
- Congenital Anomalies and Fetal Surgery 4

Co-authors: Robert Saura Didier Lacombe Hubert de Verneuil François Moreau‐Gaudry J. Horovitz Benoı̂t Arveiler B. Maugey‐Laulom Denis Roux
Cited by: Developmental Biology Genetics Pediatrics, Perinatology and Child Health
Journals: Hepatology (1 paper)The American Journal of Human Genetics (1 paper)The American Journal of Surgical Pathology (1 paper)
Partner nations: France Spain United Kingdom

In The Last Decade

Laurence Taine

46 papers receiving 856 citations

Peers

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

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

All Works

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20 of 20 papers shown

#	Work
1	Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP mutations Clinical Genetics ·Julien Van‐Gils,Sophie Naudion,Jérôme Toutain,Gwenaëlle Lancelot,Tania Attié‐Bitach,Sophie Blesson,Bénédicte Demeer,Bérénice Doray,Marie Gonzalès,Jelena Martinović,Sandra Whalen,Laurence Taine,Benoı̂t Arveiler,Didier Lacombe,Patricia Fergelot	2019	8
2	Proportion of Parents Agreeing to Delay Fetal Karyotyping until the Third Trimester of Pregnancy in Cases with an Indication Fetal Diagnosis and Therapy ·Jérôme Toutain,Marie-Anne Lemaire-Coustel,Marianne Begorre,Orianne Montaubin,Gwendoline Soler,Laurence Taine,J. Horovitz,Robert Saura	2012	1
3	An unusual chromosome 22q11 deletion associated with an apparent complementary ring chromosome in a phenotypically normal woman European Journal of Medical Genetics ·Jérôme Toutain,Laurence Taine,Fanny Morice‐Picard,Houria Hallal,Zong-Qi Dai,Benoı̂t Arveiler,Didier Lacombe,J. Horovitz,Robert Saura	2011	1
4	Rheumatologic and neurological events in an elderly patient with tricho-rhino-phalangeal syndrome type I European Journal of Medical Genetics ·M. Rué,Hermann‐Josef Lüdecke,Igor Sibon,Christophe Richez,Laurence Taine,Alexandra Foubert‐Samier,Benoı̂t Arveiler,Thierry Schaeverbeke,Didier Lacombe,François Tison,Cyril Goizet	2011	6
5	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 ·Élodie Richard,François Moreau‐Gaudry,Magalie Lalanne,Isabelle Lamrissi‐Garcia,Muriel Cario,Veronique Guyonnet‐Dupérat,Laurence Taine,Cécile Ged,Hubert de Verneuil	2008	37
6	Molecular cytogenetic characterization of terminal 14q32 deletions in two children with an abnormal phenotype and corpus callosum hypoplasia European Journal of Human Genetics ·Anouck Schneider,Brigitte Benzacken,Agnès Guichet,Alain Verloès,Dominique Bonneau,Nathalie Collot,Florence Dastot-Le-Moal,Michel Goossens,Laurence Taine,Emilie Landais,Dominique Gaillard,Martine Doco‐Fenzy	2008	21
7	Combination of WAGR and Potocki–Shaffer contiguous deletion syndromes in a patient with an 11p11.2–p14 deletion European Journal of Human Genetics ·Dominique Brémond‐Gignac,John A. Crolla,Henri Copin,Agnès Guichet,Dominique Bonneau,Laurence Taine,Didier Lacombe,Clarisse Baumann,Brigitte Benzacken,Alain Verloès	2005	32
8	Prenatal diagnosis and management of sex chromosome aneuploidy: a report on 98 cases Prenatal Diagnosis ·J.-L. Brun,Flore Gangbo,Zon Qi Wen,Katia Galant,Laurence Taine,B. Maugey‐Laulom,Denis Roux,Raphaëlle Mangione,J. Horovitz,Robert Saura	2004	51
9	Molecular characterization of an 11q14.3 microdeletion associated with leukodystrophy European Journal of Human Genetics ·Cyril Goizet,Isabelle Coupry,Caroline Rooryck,Laurence Taine,Virginie Dormoy,Didier Lacombe,Benoı̂t Arveiler	2004	9
10	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 ·B. Vergier,Marc‐Antoine Belaud‐Rotureau,Marie‐Noëlle Benassy,M. Beylot‐Barry,Pierre Dubus,M Delaunay,Jean-Christophe Garroste,Laurence Taine,Jean‐Philippe Merlio	2004	23
11	Feasibility, accuracy and safety of chorionic villus sampling: a report of 10 741 cases Prenatal Diagnosis ·J.-L. Brun,Raphaëlle Mangione,Flore Gangbo,Frédéric Guyon,Laurence Taine,Denis Roux,B. Maugey‐Laulom,J. Horovitz,Robert Saura	2003	43
12	Successful therapeutic effect in a mouse model of erythropoietic protoporphyria by partial genetic correction and fluorescence-based selection of hematopoietic cells Gene Therapy ·Antonio Fontanellas,Manuel Méndez,Frédéric Mazurier,Muriel Cario,Susana Navarro,Cécile Ged,Laurence Taine,Fabien Géronimi,Élodie Richard,François Moreau‐Gaudry,Rafael Enrı́quez de Salamanca,Hubert de Verneuil	2001	22
13	Gene Therapy of a Mouse Model of Protoporphyria with a Self-Inactivating Erythroid-Specific Lentiviral Vector without Preselection Molecular Therapy ·Emmanuel Richard,Manuel Méndez,Frédéric Mazurier,Carine Morel,Pierre Costet,Ping Xia,Antonio Fontanellas,Fabien Géronimi,Muriel Cario,Laurence Taine,Cécile Ged,Punam Malik,Hubert de Verneuil,François Moreau‐Gaudry	2001	49
14	Pregnancy Outcome and Prognosisin Fetuses with Increased First-TrimesterNuchal Translucency Fetal Diagnosis and Therapy ·R. Mangione,Frédéric Guyon,Laurence Taine,Zong Qi Wen,Denis Roux,A. Vergnaud,B. Maugey‐Laulom,J. Horovitz,Robert Saura	2001	32
15	Mapping, Characterization, and Expression Analysis of the SM-20 Human Homologue, C1orf12, and Identification of a Novel Related Gene, SCAND2 Genomics ·Denis Dupuy,Incarnation Aubert,Véronique Guyonnet Dupérat,Joëlle Petit,Laurence Taine,Marianne Stef,Bertrand Bloch,Benoı̂t Arveiler	2000	32
16	High-Resolution Integrated Map Encompassing the Breast Cancer Loss of Heterozygosity Region on Human Chromosome 16q22.1 Genomics ·Eirik Frengen,Philippe Rocca‐Serra,Sergey Shaposhnikov,Laurence Taine,Jim Thorsen,Christophe Bepoldin,Martin Krekling,D Lafon,Kaja Klykken,Azza Abd El Monéim,Henning Johansen,Michel Longy,Hans Prydz,Françoise Dorion-Bonnet	2000	12
17	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 ·Frédéric Mazurier,Antonio Fontanellas,Stéphanie Salesse,Laurence Taine,S Landriau,François Moreau‐Gaudry,Josy Reiffers,Bruno Péault,James P. Di Santo,Hubert de Verneuil	1999	94
18	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 ·Valérie Biancalana,Laurence Taine,J. Bouix,Sonja Finck,Alain Chauvin,Hubert de Verneuil,Samantha J.L. Knight,Claude Stoll,Didier Lacombe,Jean‐Louis Mandel	1996	24
19	PRENATAL DIAGNOSIS IN CONGENITAL ERYTHROPOIETIC PORPHYRIA BY METABOLIC MEASUREMENT AND DNA MUTATION ANALYSIS Prenatal Diagnosis ·Cécile Ged,François Moreau‐Gaudry,Laurence Taine,Isabelle Hombrados,Patrick Calvas,P Colombiès,Hubert de Verneuil	1996	22
20	Chromosome analysis of adenomatous polyps of the colon Cancer Genetics and Cytogenetics ·Michel Longy,Robert Saura,F Dumas,Jean-François Leseve,Laurence Taine,Jean‐François Goussot,Patrice Couzigou	1993	25

About Laurence Taine

Laurence Taine is a scholar working on Developmental Biology, Genetics and Pediatrics, Perinatology and Child Health, having authored 46 papers that have together received 924 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (14 papers), Prenatal Screening and Diagnostics (9 papers), Porphyrin Metabolism and Disorders (6 papers), RNA modifications and cancer (6 papers), Congenital limb and hand anomalies (5 papers), Genetics and Neurodevelopmental Disorders (5 papers), Congenital Anomalies and Fetal Surgery (4 papers) and Virus-based gene therapy research (3 papers). The work is most often cited by research in Developmental Biology (86 citations), Genetics (398 citations) and Pediatrics, Perinatology and Child Health (274 citations). Laurence Taine has collaborated with scholars based in France, Spain and United Kingdom. Frequent 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. Their work appears in journals such as Hepatology, The American Journal of Human Genetics and The American Journal of Surgical Pathology.

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