Anouck Schneider

742 total citations
21 papers, 355 citations indexed

About

Anouck Schneider is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Anouck Schneider has authored 21 papers receiving a total of 355 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 13 papers in Molecular Biology and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Anouck Schneider's work include Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Anouck Schneider is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Anouck Schneider collaborates with scholars based in France, United States and United Kingdom. Anouck Schneider's co-authors include Jacques Puechberty, Franck Pellestor, Vincent Gâtinois, Dominique Gaillard, David Geneviève, Martine Doco‐Fenzy, Emilie Landais, B. Hédon, T. Anahory and Jacques Motté and has published in prestigious journals such as Human Reproduction, Fertility and Sterility and Transplantation.

In The Last Decade

Anouck Schneider

19 papers receiving 341 citations

Peers

Countries citing papers authored by Anouck Schneider

Since Specialization

Citations

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

Fields of papers citing papers by Anouck Schneider

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anouck Schneider

This figure shows the co-authorship network connecting the top 25 collaborators of Anouck Schneider. A scholar is included among the top collaborators of Anouck Schneider 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 Anouck Schneider. Anouck Schneider 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	Confined placental mosaicism is a diagnostic pitfall in dystrophinopathies: a clinical report 2024 ·European Journal of Human Genetics ·(unknown), (unknown), Anouck Schneider, (unknown), Marie‐Claire Vincent, Christine Coubes, Jacques Puechberty, (unknown), Michel Kœnig, Franck Pellestor, Mireille Cossée, Vincent Gâtinois	0
2	Chromoanagenesis, the mechanisms of a genomic chaos 2021 ·Seminars in Cell and Developmental Biology ·Franck Pellestor, (unknown), Anouck Schneider, Jacques Puechberty, Vincent Gâtinois	47
3	Mosaic complete tetrasomy 21 in a fetus with complete atrioventricular septal defect and minor morphological variations 2019 ·Molecular Genetics & Genomic Medicine ·Vincent Gâtinois, Nicole Bigi, E. Mousty, Jean Chiésa, (unknown), Anouck Schneider, Geneviève Lefort, Lucile Pinson, (unknown), (unknown), (unknown), (unknown), Patricia Blanchet, Carole Corsini, (unknown), Patrick Callier, David Geneviève, Franck Pellestor, Jacques Puechberty	0
4	Disruption of chromatin organisation causes MEF2C gene overexpression in intellectual disability: a case report 2019 ·BMC Medical Genomics ·Kévin Yauy, Anouck Schneider, Bee Ling Ng, (unknown), Satish Sati, Christine Coubes, Constance Wells, (unknown), Thomas Guignard, (unknown), David Geneviève, Jacques Puechberty, Franck Pellestor, Vincent Gâtinois	8
5	Looking for Broken TAD Boundaries and Changes on DNA Interactions: Clinical Guide to 3D Chromatin Change Analysis in Complex Chromosomal Rearrangements and Chromothripsis 2018 ·Methods in molecular biology ·Kévin Yauy, Vincent Gâtinois, Thomas Guignard, Satish Sati, Jacques Puechberty, (unknown), Anouck Schneider, Franck Pellestor	5
6	Is the resulting phenotype of an embryo with balanced X-autosome translocation, obtained by means of preimplantation genetic diagnosis, linked to the X inactivation pattern? 2016 ·Fertility and Sterility ·F. Ferfouri, (unknown), Anouck Schneider, (unknown), B. Hédon, T. Anahory	19
7	Identification of disrupted AUTS2 and EPHA6 genes by array painting in a patient carrying a de novo balanced translocation t(3;7) with intellectual disability and neurodevelopment disorder 2015 ·American Journal of Medical Genetics Part A ·Anouck Schneider, Jacques Puechberty, Bee Ling Ng, Christine Coubes, Vincent Gâtinois, (unknown), Manon Girard, Bruno Dumont, (unknown), (unknown), Amaria Baghdadli, Franck Pellestor, David Geneviève	8
8	Discordant sex in monozygotic XXY/XX twins: a case report 2014 ·Human Reproduction ·Guillaume Tachon, G. Lefort, Jacques Puechberty, Anouck Schneider, C. Jeandel, P. Boulot, O. Prodhomme, Pierre Meyer, Sylvie Taviaux, Isabelle Touitou, Franck Pellestor, David Geneviève, Vincent Gâtinois	13
9	CEP57 mutation in a girl with mosaic variegated aneuploidy syndrome 2013 ·American Journal of Medical Genetics Part A ·Lucile Pinson, Linda Mannini, Marjolaine Willems, Francesco Cucco, Nicolas Sirvent, Thierry Frébourg, Valentina Quarantotti, Corinne Collet, Anouck Schneider, Pierre Sarda, David Geneviève, Jacques Puechberty, Geneviève Lefort, Antonio Musio	20
10	Somatic mosaicism in trichorhinophalangeal syndrome: a lesson for genetic counseling 2013 ·European Journal of Human Genetics ·Carole Corsini, Martin Genčík, Marjolaine Willems, Eva L. Decker, Elodie Sanchez, Jacques Puechberty, Anouck Schneider, Manon Girard, Patrick Edery, (unknown), J. Cottalorda, Geneviève Lefort, Claire Jeandel, Pierre Sarda, David Geneviève	2
11	Expanding the phenotype of IQSEC2 mutations: truncating mutations in severe intellectual disability 2013 ·European Journal of Human Genetics ·Frédéric Tran Mau‐Them, Marjolaine Willems, Beate Albrecht, Elodie Sanchez, Jacques Puechberty, Sabine Endele, Anouck Schneider, (unknown), Chantal Missirian, François Rivier, Manon Girard, Muriel Holder, Sylvie Manouvrier, Isabelle Touitou, Geneviève Lefort, Pierre Sarda, Anne Moncla, Séverine Drunat, Dagmar Wieczorek, David Geneviève	30
12	Analysis using fish of sperm and embryos from two carriers of rare rob(13;21) and rob(15;22) robertsonian translocation undergoing PGD 2012 ·European Journal of Medical Genetics ·(unknown), Anouck Schneider, (unknown), S. Hamamah, B. Hédon, Franck Pellestor, T. Anahory	13
13	Duplication 8q12: confirmation of a novel recognizable phenotype with duane retraction syndrome and developmental delay 2012 ·European Journal of Human Genetics ·(unknown), Marie Vincent, Patricia Blanchet, Jacques Puechberty, Anouck Schneider, (unknown), Manon Girard, (unknown), Christian Jørgensen, Denis Morin, Pierre Sarda, Geneviève Lefort, David Geneviève	16
14	Bipolar affective disorder and early dementia onset in a male patient with SHANK3 deletion 2012 ·European Journal of Medical Genetics ·(unknown), Emilie Landais, (unknown), (unknown), Anouck Schneider, (unknown), (unknown), Jacques Motté, Dominique Gaillard, (unknown), Martine Doco‐Fenzy	43
15	Epiphyseal punctate calcifications (stippling) in complete trisomy 9 2009 ·Prenatal Diagnosis ·(unknown), Anouck Schneider, Anne‐Marie Chaze, Nicole Bigi, Geneviève Lefort, Caroline Rouleau, (unknown), (unknown), (unknown), A. Couture, Pierre Boulot, Patricia Blanchet, Pierre Sarda, David Geneviève	2
16	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
17	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
18	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
19	Pure direct duplication (12)(q24.1 → q24.2) in a child with Marcus Gunn phenomenon and multiple congenital anomalies 2006 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), (unknown), (unknown), Nathalie Bednarek, Stéphanie Struski, Juliette Albuisson, (unknown), Nathalie Collot, Anouck Schneider, Florence Dastot‐Le Moal, Dominique Gaillard, Michel Goossens	28
20	Characteristic Pattern of Chromosomal Imbalances in Posttransplantation Lymphoproliferative Disorders: Correlation with Histopathological Subcategories and EBV Status 2005 ·Transplantation ·Hélène A. Poirel, Alain Bernheim, Anouck Schneider, Mounira Meddeb, Sylvain Choquet, Véronique Leblond, Frédéric Charlotte, Frédéric Davi, Danielle Canioni, Elizabeth Macintyre, Marie‐France Mamzer, (unknown), Olivier Hermine, Antoine Martin, Pascale Cornillet‐Lefèbvre, Martine Patey, Olivier Toupance, Jean‐Louis Kémény, P. Deteix, Martine Raphaël	55

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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