Martine Doco‐Fenzy

3.5k total citations
29 papers, 690 citations indexed

About

Martine Doco‐Fenzy is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Martine Doco‐Fenzy has authored 29 papers receiving a total of 690 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 16 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Martine Doco‐Fenzy's work include Genomic variations and chromosomal abnormalities (14 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genomics and Rare Diseases (4 papers). Martine Doco‐Fenzy is often cited by papers focused on Genomic variations and chromosomal abnormalities (14 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genomics and Rare Diseases (4 papers). Martine Doco‐Fenzy collaborates with scholars based in France, United States and United Kingdom. Martine Doco‐Fenzy's co-authors include Stéphanie Struski, Pascale Cornillet‐Lefèbvre, Dominique Gaillard, Emilie Landais, Aude Lallemand, Céline Poirsier, Marta Spodenkiewicz, Anne-Sophie Lèbre, Anouck Schneider and Jacques Motté and has published in prestigious journals such as Human Molecular Genetics, Molecular Biology of the Cell and Journal of Medical Genetics.

In The Last Decade

Martine Doco‐Fenzy

28 papers receiving 661 citations

Peers

Countries citing papers authored by Martine Doco‐Fenzy

Since Specialization

Citations

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

Fields of papers citing papers by Martine Doco‐Fenzy

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Martine Doco‐Fenzy. 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 Martine Doco‐Fenzy. The network helps show where Martine Doco‐Fenzy may publish in the future.

Co-authorship network of co-authors of Martine Doco‐Fenzy

This figure shows the co-authorship network connecting the top 25 collaborators of Martine Doco‐Fenzy. A scholar is included among the top collaborators of Martine Doco‐Fenzy 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 Martine Doco‐Fenzy. Martine Doco‐Fenzy 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	Interprétation des résultats issus du séquençage à haut débit pour les maladies génétiques 2024 ·médecine/sciences ·Svetlana Gorokhova, Cécile Rouzier, Cécile Acquaviva, Stéphanie Baert‐Desurmont, Sandrine M. Caputo, (unknown), Florence Coulet, Martine Doco‐Fenzy, Boris Keren, Cédric Le Maréchal, Gaël Nicolas, Vincent Procaccio, Pascale Richard, Pauline Romanet, (unknown), Jean Muller, (unknown), Pascale Saugier-Véber	0
2	Hepatotoxicity of metronidazole in Cockayne syndrome: A clinical report 2021 ·European Journal of Medical Genetics ·(unknown), Camille Boulagnon‐Rombi, (unknown), Martine Doco‐Fenzy, Gérard Thiéfin	3
3	Report on 3 patients with 12p duplication including GRIN2B 2014 ·European Journal of Medical Genetics ·Céline Poirsier, Emilie Landais, Nathalie Bednarek, (unknown), Maroun Khoury, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Dominique Gaillard, Martine Doco‐Fenzy	16
4	Novel mutational mechanism in the thyroglobulin gene: Imperfect DNA inversion as a cause for hereditary hypothyroidism 2013 ·Molecular and Cellular Endocrinology ·Cintia E. Citterio, Liliana Carmen Rossetti, (unknown), (unknown), (unknown), (unknown), (unknown), Martine Doco‐Fenzy, Rogelio González‐Sarmiento, (unknown), Carlos Daniel De Brasi, Héctor M. Targovnik	14
5	Loss of function of KIAA2022 causes mild to severe intellectual disability with an autism spectrum disorder and impairs neurite outgrowth 2013 ·Human Molecular Genetics ·Lionel Van Maldergem, Qingming Hou, Vera M. Kalscheuer, Marlène Rio, Martine Doco‐Fenzy, Ana Medeira, Arjan P.M. de Brouwer, Christelle Cabrol, Stefan A. Haas, Pierre Cacciagli, Sébastien Moutton, Emilie Landais, Jacques Motté, Laurence Colleaux, Céline Bonnet, Laurent Villard, Juliette Dupont, Heng‐Ye Man	55
6	Sirenomelia: A new type, Showing VACTERL Association with thomas syndrome and a review of literature 2013 ·Birth Defects Research Part A Clinical and Molecular Teratology ·(unknown), (unknown), Camille Boulagnon‐Rombi, (unknown), Martine Doco‐Fenzy, Dominique Gaillard, (unknown), Claude Avisse, Marc Labrousse	12
7	KBP–cytoskeleton interactions underlie developmental anomalies in Goldberg–Shprintzen syndrome 2013 ·Human Molecular Genetics ·(unknown), André Mégarbané, Bénédicte Demeer, (unknown), Paule Bénit, Audrey Briand‐Suleau, (unknown), Jamal Ghoumid, (unknown), Xavier Decrouy, Martine Doco‐Fenzy, Pierre Rustin, Dominique Gaillard, Michel Goossens, Irina Giurgea	24
8	A 5.3 Mb deletion in chromosome 18q12.3 as the smallest region of overlap in two patients with expressive speech delay 2010 ·European Journal of Medical Genetics ·Sonia Bouquillon, Joris Andrieux, Emilie Landais, Bénédicte Duban‐Bedu, (unknown), (unknown), Louis Vallée, Teresinha Leal, Martine Doco‐Fenzy, Bruno Delobel	21
9	Genotype–phenotype correlation in four 15q24 deleted patients identified by array‐CGH 2009 ·American Journal of Medical Genetics Part A ·Joris Andrieux, Christèle Dubourg, Marlène Rio, Tania Attié‐Bitach, Elsa Delaby, Michèle Mathieu, Hubert Journel, Henri Copin, (unknown), Martine Doco‐Fenzy, Emilie Landais, Bruno Delobel, Sylvie Odent, Sylvie Manouvrier‐Hanu, Muriel Holder‐Espinasse	27
10	Deletion 2q36.2q36.3 with multiple renal cysts and severe mental retardation 2008 ·European Journal of Medical Genetics ·Martine Doco‐Fenzy, Emilie Landais, Joris Andrieux, Anouck Schneider, Brigitte Delemer, V. Sulmont, (unknown), Dominique Ploton, (unknown), Jean‐Claude Monboisse, M. Belouadah, (unknown), A. Durlach, Michel Goossens, Juliette Albuisson, Jacques Motté, Dominique Gaillard	8
11	Molecular cytogenetic characterization of terminal 14q32 deletions in two children with an abnormal phenotype and corpus callosum hypoplasia 2008 ·European Journal of Human Genetics ·Anouck Schneider, Brigitte Benzacken, Agnès Guichet, Alain Verloès, Dominique Bonneau, Nathalie Collot, (unknown), Michel Goossens, Laurence Taine, Emilie Landais, Dominique Gaillard, Martine Doco‐Fenzy	21
12	Collapsing glomerulopathy in Galloway–Mowat syndrome: A case report and review of the literature 2008 ·Pathology - Research and Practice ·Hervé Sartelet, Christine Piètrement, Laure‐Hélène Noël, Pascal Sabouraud, Philippe Birembaut, Luc L. Oligny, Bernard Roussel, Martine Doco‐Fenzy	11
13	The clinical spectrum associated with a chromosome 17 short arm proximal duplication (dup 17p11.2) in three patients 2008 ·American Journal of Medical Genetics Part A ·Martine Doco‐Fenzy, Muriel Holder‐Espinasse, Éric Bieth, Corinne Magdelaine, Marie‐Claire Vincent, Maroun Khoury, Joris Andrieux, Feng Zhang, James R. Lupski, Rabih Klink, Anouck Schneider, (unknown), Jean‐Marie Cuisset, Louis Vallée, Sylvie Manouvrier‐Hanu, Dominique Gaillard, Bérengère de Martinville	11
14	Subtelomeric imbalances in phenotypically normal individuals 2007 ·Human Mutation ·Irina Balikova, Björn Menten, Thomy de Ravel, Cédric Le Caignec, Bernard Thienpont, (unknown), Martine Doco‐Fenzy, Marjan De Rademaeker, Geert Mortier, R. Frank Kooy, (unknown), Koenraad Devriendt, Jean‐Pierre Fryns, Frank Speleman, Joris Vermeesch	62
15	Cytogenetic Evolution of Human Ovarian Cell Lines Associated with Chemoresistance and Loss of Tumorigenicity 2003 ·Analytical Cellular Pathology ·Stéphanie Struski, Martine Doco‐Fenzy, Michael Köehler, Ilse Chudoba, F. Lévy, (unknown), (unknown), (unknown), (unknown), Jean Bénard, G Potron, Pascale Cornillet‐Lefèbvre	3
16	Compilation of published comparative genomic hybridization studies 2002 ·Cancer Genetics and Cytogenetics ·Stéphanie Struski, Martine Doco‐Fenzy, Pascale Cornillet‐Lefèbvre	104
17	Cytogenetic characterization of chromosomal rearrangement in a human vinblastine-resistant CEM cell line 2002 ·Cancer Genetics and Cytogenetics ·Stéphanie Struski, Pascale Cornillet‐Lefèbvre, Martine Doco‐Fenzy, Jean Dufer, (unknown), (unknown), (unknown), (unknown), G Potron	15
18	Identification of chromosomal loci associated with non-P-glycoprotein-mediated multidrug resistance to topoisomerase II inhibitor in lung adenocarcinoma cell line by comparative genomic hybridization 2001 ·Genes Chromosomes and Cancer ·Stéphanie Struski, Martine Doco‐Fenzy, (unknown), (unknown), (unknown), (unknown), (unknown), Jean‐Claude Jardillier, G Potron, Pascale Cornillet‐Lefèbvre	13
19	Electron Tomography of Metaphase Nucleolar Organizer Regions: Evidence for a Twisted-Loop Organization 1997 ·Molecular Biology of the Cell ·Laurent Héliot, Hervé Kaplan, Laurent Lucas, Christophe Klein, A. Beorchia, Martine Doco‐Fenzy, M. Menager, Marc Thiry, Marie-Françoise O’Donohue, Dominique Ploton	58
20	Viral integration sites in human papilloma virus-33-immortalized cervical keratinocyte cell lines 1996 ·Cancer Genetics and Cytogenetics ·Christine Gilles, Jacques Piette, Dominique Ploton, Martine Doco‐Fenzy, Jean‐Michel Foidart	15

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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