Sylvie Manouvrier

5.4k citations

52 papers · 921 indexed · h-index 16

Molecular Biology
Genetics top 5%
Cancer Research top 10%
Surgery
Pediatrics, Perinatology and Child Health top 10%

Co-authors: Stanislas Lyonnet Arnold Münnich David Geneviève Loïc de Pontual Arie van Haeringen Patrick Callier Alice Goldenberg Jeanne Amiel
Topics: Prenatal Screening and Diagnostics (12 papers)Congenital Anomalies and Fetal Surgery (7 papers)Genetic factors in colorectal cancer (7 papers)
Cited by: Developmental Biology Cancer Research Genetics
Journals: Nature Genetics PLoS ONE The American Journal of Human Genetics
Partner nations: France United States Netherlands

In The Last Decade

Sylvie Manouvrier

47 papers receiving 891 citations

Peers

Countries citing papers authored by Sylvie Manouvrier

Since Specialization

Citations

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

Fields of papers citing papers by Sylvie Manouvrier

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sylvie Manouvrier

This figure shows the co-authorship network connecting the top 25 collaborators of Sylvie Manouvrier. A scholar is included among the top collaborators of Sylvie Manouvrier 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 Sylvie Manouvrier. Sylvie Manouvrier 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	RPL26 variants: A rare cause of Diamond-Blackfan anemia syndrome with multiple congenital anomalies at the forefront 2024 ·Genetics in Medicine ·Clémence Vanlerberghe,Frédéric Frénois,Thomas Smol,Anne‐Sophie Jourdain,Fabienne Escande,Emilie Ait‐Yahya,Abdulrahman Aldeeri,Timothy W. Yu,Valérie Cormier‐Daire,Jamal Ghoumid,(unknown),(unknown),Sylvie Manouvrier,(unknown),Sebastian Sailer,Perrine Brunelle,(unknown),Florence Petit	0
2	Le test de concordance de script à l’heure de la réforme du second cycle des études médicales en France : étude pilote en génétique médicale 2021 ·Pédagogie médicale ·Jamal Ghoumid,Thomas Smol,(unknown),(unknown),Perrine Brunelle,(unknown),Alexandre Louvet,Dominique Lacroix,Didier Gosset,Sylvie Manouvrier,Florence Petit,L. Sibert	0
3	Syndrome de Lynch et risque de cancer de la prostate ; revue de la littérature 2015 ·Progrès en Urologie ·F. Maillard,Sylvie Manouvrier,Xavier Biardeau,A. Ouzzane,Arnauld Villers	2
4	Screening of MAMLD1 Mutations in 70 Children with 46,XY DSD: Identification and Functional Analysis of Two New Mutations 2012 ·PLoS ONE ·Nicolas Kalfa,Maki Fukami,Pascal Philibert,Françoise Audran,Catherine Pienkowski,Jacques Weill,Graziella Pinto,Sylvie Manouvrier,Michel Polak,Tsutomu Ogata,Charles Sultan	29
5	Evidence of constitutional MLH1 epimutation associated to transgenerational inheritance of cancer susceptibility 2011 ·Human Mutation ·Michel Crépin,(unknown),Sophie Lejeune,Fabienne Escande,(unknown),Nicole Porchet,Gilles Morin,Sylvie Manouvrier,Michèle Mathieu,Marie‐Pierre Buisine	47
6	Genetic testing for hereditary cancer: Effects of alexithymia and coping strategies on variations in anxiety before and after result disclosure 2011 ·Psychology and Health ·Carole Fantini‐Hauwel,Bruno Dauvier,Thomas Arciszewski,Pascal Antoine,Sylvie Manouvrier	11
7	Germline deletion of the miR-17∼92 cluster causes skeletal and growth defects in humans 2011 ·Nature Genetics ·Loïc de Pontual,Evelyn Yao,Patrick Callier,Laurence Faivre,Valérie Drouin,(unknown),Arie van Haeringen,David Geneviève,Alice Goldenberg,Myriam Oufadem,Sylvie Manouvrier,Arnold Münnich,Joana A. Vidigal,Michel Vekemans,Stanislas Lyonnet,Alexandra Henrion‐Caude,Andrea Ventura,Jeanne Amiel	226
8	Étude de la vulnérabilité psychologique des sujets inscrits à un dépistage génétique des cancers colorectaux héréditaires 2007 ·L Encéphale ·Carole Fantini‐Hauwel,Jean-Louis Pédinielli,Sylvie Manouvrier	1
9	Low frequency ofAXIN2 mutations and high frequency ofMUTYH mutations in patients with multiple polyposis 2006 ·Human Mutation ·Sophie Lejeune,François Guillemot,Jean–Pierre Triboulet,Stéphane Cattan,C. Mouton,(unknown),Nicole Porchet,Sylvie Manouvrier,Marie‐Pierre Buisine	36
10	Forme respiratoire néonatale létale de la maladie de Niemann-Pick C2 et diagnostic anténatal par l'étude des mutations du gène HE1/NPC2 2005 ·Archives de Pédiatrie ·(unknown),Gilles Millat,(unknown),(unknown),(unknown),D. Dobbelaere,Lucie Vérot,(unknown),Claudine Le Vaillant,Frédèric Gottrand,E. Bogaert,(unknown),S Klosowski,(unknown),(unknown),Sylvie Manouvrier,M. T. Vanier	10
11	Metaphyseal chondrodysplasia with cone‐shaped epiphyses: A specific form involving the lower limbs 2003 ·American Journal of Medical Genetics Part A ·Anne Dieux‐Coëslier,Alexandre Moerman,Muriel Holder,Odile Boute,P Maroteaux,Sylvie Manouvrier,Martine Le Merrer	3
12	Alveolar capillary dysplasia: a cause of persistent pulmonary hypertension of the newborn 2002 ·European Journal of Pediatrics ·(unknown),(unknown),Louise Devisme,Patrick Truffert,Thameur Rakza,Yvon Riou,Sylvie Manouvrier,P Lequien,Laurent Storme	39
13	Autosomal Recessive Disorder Otospondylomegaepiphyseal Dysplasia Is Associated with Loss-of-Function Mutations in the COL11A2 Gene 2000 ·The American Journal of Human Genetics ·(unknown),Han G. Brunner,Sylvie Manouvrier,Raoul C. M. Hennekam,Andrea Superti‐Furga,Helena Kääriäinen,Richard M. Pauli,Ton van Essen,Matthew L. Warman,Jacky Bonaventure,Peter Miny,Leena Ala‐Kokko	60
14	Identification of novelL1CAM mutations using fluorescence-assisted mismatch analysis 1998 ·Human Mutation ·Pascale Saugier-Véber,Cosette Martin,Nathalie Le Meur,Stanislas Lyonnet,Arnold Munnich,Albert David,(unknown),Delphine Héron,Philippe Jonveaux,Sylvie Odent,Sylvie Manouvrier,Anne Moncla,Nicole Morichon,Nicole Philip,Daniel Satgé,Mario Tosi,Thierry Frébourg	22
15	Brachmann-de Lange syndrome: Pre- and postnatal findings 1996 ·American Journal of Medical Genetics ·Sylvie Manouvrier,(unknown),P. Vaast,Odile Boute,(unknown),(unknown),F Puech,B Gosselin,J. P. Farriaux	22
16	Embryofœtopathie au valproate : une pathologie encore trop mal connue. À propos de quatre observations 1996 ·Archives de Pédiatrie ·(unknown),Sylvie Manouvrier,Odile Boute,J. P. Farriaux	8
17	PRENATAL DIAGNOSIS OF ROBERTS SYNDROME: TWO NEW CASES 1996 ·Prenatal Diagnosis ·Brigitte Benzacken,(unknown),Sylvie Manouvrier,Martine Bucourt,(unknown)	10
18	Dyssegmental dysplasia with glaucoma 1996 ·American Journal of Medical Genetics ·P Maroteaux,Sylvie Manouvrier,Jacky Bonaventure,Martine Le Merrer	3
19	Prenatal Diagnosis of Thrombocytopenia-Absent Radius Syndrome 1996 ·Fetal Diagnosis and Therapy ·Odile Boute,S Depret-Mosser,D. Vinatier,Sylvie Manouvrier,(unknown),J. P. Farriaux,Jean-Marie Monnier	12
20	Trisomy 16q23?qter arising from a maternal t(13;16)(p12;q23): case report and evidence of the reciprocal balanced maternal rearrangement by the Ag-NOR technique 1991 ·Human Genetics ·(unknown),Francis Vasseur,Sylvie Manouvrier,Agnès Daudignon,(unknown),(unknown),(unknown),P Lequien,(unknown)	19

About Sylvie Manouvrier

Sylvie Manouvrier is a scholar working on Developmental Biology, Pediatrics, Perinatology and Child Health and Genetics, having authored 52 papers that have together received 921 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (12 papers), Congenital Anomalies and Fetal Surgery (7 papers) and Genetic factors in colorectal cancer (7 papers). The work is most often cited by research in Developmental Biology (56 citations), Cancer Research (211 citations) and Genetics (359 citations). Sylvie Manouvrier has collaborated with scholars based in France, United States and Netherlands. Frequent co-authors include Stanislas Lyonnet, Arnold Münnich, David Geneviève, Loïc de Pontual, Arie van Haeringen, Patrick Callier, Alice Goldenberg, Jeanne Amiel, Laurence Faivre and Joana A. Vidigal. Their work appears in journals such as Nature Genetics, PLoS ONE and The American 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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