Laëtitia Gouas

1.5k citations

36 papers · 705 indexed · h-index 13

Co-authors: Pascale Guicheney Philippe Vago Carole Goumy Andréï Tchirkov Anne Forhan Myriam Berthet Viviane Nicaud Beverley Balkau
Topics: Genomic variations and chromosomal abnormalities (18 papers)Prenatal Screening and Diagnostics (12 papers)Chromosomal and Genetic Variations (7 papers)
Cited by: Cardiology and Cardiovascular Medicine Molecular Biology Genetics
Journals: Human Molecular Genetics Gene Cardiovascular Research
Partner nations: France Canada Algeria

In The Last Decade

Laëtitia Gouas

33 papers receiving 662 citations

Peers

Countries citing papers authored by Laëtitia Gouas

Since Specialization

Citations

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

Fields of papers citing papers by Laëtitia Gouas

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laëtitia Gouas

This figure shows the co-authorship network connecting the top 25 collaborators of Laëtitia Gouas. A scholar is included among the top collaborators of Laëtitia Gouas 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 Laëtitia Gouas. Laëtitia Gouas 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	Optical genome mapping for prenatal diagnosis: A prospective study 2023 ·Clinica Chimica Acta ·Carole Goumy,(unknown),Gwendoline Soler,Éléonore Eymard-Pierre,Hélène Laurichesse,A. Delabaere,D. Gallot,(unknown),Isabelle Perthus,Céline Pebrel‐Richard,Laëtitia Gouas,(unknown),Jérôme Salse,Lauren Véronèse,Andréï Tchirkov	12
2	Reduced telomere length in amniocytes: an early biomarker of abnormal fetal development? 2022 ·Human Molecular Genetics ·Carole Goumy,Lauren Véronèse,(unknown),(unknown),(unknown),Denis Gallot,Hélène Laurichesse,A. Delabaere,Laëtitia Gouas,(unknown),(unknown),Philippe Vago,Andréï Tchirkov	5
3	Spatial organization of chromosome territories in the interphase nucleus of trisomy 21 cells 2017 ·Chromosoma ·(unknown),Christophe Tatout,(unknown),Céline Pebrel‐Richard,Carole Goumy,(unknown),(unknown),(unknown),Philippe Vago,Laëtitia Gouas	16
4	Congenital diaphragmatic hernia may be associated with 17q12 microdeletion syndrome 2014 ·American Journal of Medical Genetics Part A ·Carole Goumy,Fanny Laffargue,Éléonore Eymard-Pierre,(unknown),(unknown),Laëtitia Gouas,Denis Gallot,Christine Francannet,Andréï Tchirkov,Céline Pebrel‐Richard,Philippe Vago	19
5	Prenatal ultrasound diagnosis of a 48,XXYY syndrome 2013 ·Morphologie ·(unknown),Céline Pebrel‐Richard,Laëtitia Gouas,Lauren Véronèse,D. Lémery,Andréï Tchirkov,Carole Goumy,Philippe Vago	0
6	An unusual clinical severity of 16p11.2 deletion syndrome caused by unmasked recessive mutation of CLN3 2013 ·European Journal of Human Genetics ·Céline Pebrel‐Richard,Anne Debost‐Legrand,Éléonore Eymard-Pierre,(unknown),(unknown),(unknown),Laëtitia Gouas,Andréï Tchirkov,Philippe Vago,Carole Goumy,Christine Francannet	30
7	Trisomie 21 et cancers 2012 ·Morphologie ·(unknown),Laëtitia Gouas,Frédérique Penault‐Llorca,Ahlem Amouri,Andréï Tchirkov,Philippe Vago	8
8	A new case of 8q22.1 microdeletion restricts the critical region for Nablus mask‐like facial syndrome 2012 ·American Journal of Medical Genetics Part A ·Anne Debost‐Legrand,Éléonore Eymard-Pierre,Céline Pebrel‐Richard,Laëtitia Gouas,Carole Goumy,M. Giollant,(unknown),Andréï Tchirkov,Christine Francannet,Philippe Vago	7
9	Prenatal diagnosis of a rare de novo centromeric chromosome 6 variant 2011 ·Gene ·Carole Goumy,(unknown),Éléonore Eymard-Pierre,Charles W. Richard,Laëtitia Gouas,Patricia Combes,(unknown),Denis Gallot,Andréï Tchirkov,Philippe Vago	1
10	Prenatal detection of cryptic rearrangements by multiplex ligation probe amplification in fetuses with ultrasound abnormalities 2010 ·Genetics in Medicine ·Carole Goumy,Laëtitia Gouas,Céline Pebrel‐Richard,Lauren Véronèse,Éléonore Eymard-Pierre,Anne Debost‐Legrand,(unknown),Andréï Tchirkov,Philippe Vago	6
11	De novo unbalanced translocation 2;4 characterized by metaphase CGH and array CGH in a child with mental retardation and dysmorphic features 2010 ·Pathologie Biologie ·Anne Debost‐Legrand,Yline Capri,Laëtitia Gouas,Céline Pebrel‐Richard,Lauren Véronèse,Andréï Tchirkov,(unknown),Odile Boespflug‐Tanguy,Carole Goumy,Philippe Vago	0
12	Fetal skin fibroblasts: A cell model for studying the retinoid pathway in congenital diaphragmatic hernia 2010 ·Birth Defects Research Part A Clinical and Molecular Teratology ·Carole Goumy,Karen Coste,Geoffroy Marceau,Laëtitia Gouas,(unknown),Philippe Vago,Denis Gallot,Vincent Sapin	2
13	Retinoid Pathway and Congenital Diaphragmatic Hernia: Hypothesis from the Analysis of Chromosomal Abnormalities 2010 ·Fetal Diagnosis and Therapy ·Carole Goumy,Laëtitia Gouas,Geoffroy Marceau,Karen Coste,Lauren Véronèse,Denis Gallot,Vincent Sapin,Philippe Vago,Andréï Tchirkov	34
14	SCN5A Mutations and the Role of Genetic Background in the Pathophysiology of Brugada Syndrome 2009 ·Circulation Cardiovascular Genetics ·Vincent Probst,Arthur A.M. Wilde,Julien Barc,Frédéric Sacher,Dominique Babuty,Philippe Mabo,Jacques Mansourati,Solena Le Scouarnec,Florence Kyndt,Cédric Le Caignec,Pascale Guicheney,Laëtitia Gouas,Juliette Albuisson,Paola G. Meregalli,Hervé Le Marec,Hanno L. Tan,Jean‐Jacques Schott	211
15	Strong correlation between VEGF and MCL-1 mRNA expression levels in B-cell chronic lymphocytic leukemia 2009 ·Leukemia Research ·Lauren Véronèse,Olivier Tournilhac,Pierre Verrelle,Frédéric Davi,Guillaume Dighiero,Emmanuel Chautard,Richard Veyrat‐Masson,Fabrice Kwiatkowski,Carole Goumy,Laëtitia Gouas,Jacques‐Olivier Bay,Philippe Vago,Andréï Tchirkov	17
16	Familial deletion 11q14.3–q22.1 without apparent phenotypic consequences: A haplosufficient 8.5 Mb region 2008 ·American Journal of Medical Genetics Part A ·Carole Goumy,Laëtitia Gouas,Andréï Tchirkov,(unknown),M. Giollant,Lauren Véronèse,Christine Francannet,Philippe Vago	10
17	Gene dosage methods as diagnostic tools for the identification of chromosome abnormalities 2008 ·Pathologie Biologie ·Laëtitia Gouas,Carole Goumy,Lauren Véronèse,Andréï Tchirkov,Philippe Vago	23
18	The occurrence of Brugada syndrome and isolated cardiac conductive disease in the same family could be due to a single SCN5A mutation or to the accidental association of both diseases 2007 ·EP Europace ·Isabelle Six,(unknown),Hai Huang,Laëtitia Gouas,Véronique Fressart,N. Benammar,Bernard Hainque,(unknown),Mohamed Chahine,Pascale Guicheney	12
19	Association of KCNQ1, KCNE1, KCNH2 and SCN5A polymorphisms with QTc interval length in a healthy population 2005 ·European Journal of Human Genetics ·(unknown),Laëtitia Gouas,Viviane Nicaud,Myriam Berthet,Anne Forhan,Laurence Tiret,Beverley Balkau,Pascale Guicheney	117
20	New KCNQ1 mutations leading to haploinsufficiency in a general population1Defective trafficking of a KvLQT1 mutant 2004 ·Cardiovascular Research ·Laëtitia Gouas,Chloé Bellocq,Myriam Berthet,F Potet,Sophie Demolombe,Anne Forhan,(unknown),Fernando Simón,B. Balkau,Isabelle Denjoy	49

About Laëtitia Gouas

Laëtitia Gouas is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Genetics, having authored 36 papers that have together received 705 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (18 papers), Prenatal Screening and Diagnostics (12 papers) and Chromosomal and Genetic Variations (7 papers). The work is most often cited by research in Cardiology and Cardiovascular Medicine (413 citations), Molecular Biology (471 citations) and Genetics (150 citations). Laëtitia Gouas has collaborated with scholars based in France, Canada and Algeria. Frequent co-authors include Pascale Guicheney, Philippe Vago, Carole Goumy, Andréï Tchirkov, Anne Forhan, Myriam Berthet, Viviane Nicaud, Beverley Balkau, Laurence Tiret and Lauren Véronèse. Their work appears in journals such as Human Molecular Genetics, Gene and Cardiovascular Research.

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