Sabine Sigaudy

4.4k citations

70 papers · 1.3k indexed · h-index 21

Genetics top 5%
- Genetic and Kidney Cyst Diseases 7
- Genetic Syndromes and Imprinting 6
- Genomic variations and chromosomal abnormalities 6
- Connective tissue disorders research 5
Genetics top 5%
- Genetic and Kidney Cyst Diseases 7
- Genetic Syndromes and Imprinting 6
- Genomic variations and chromosomal abnormalities 6
- Connective tissue disorders research 5
Pediatrics, Perinatology and Child Health top 5%
- Prenatal Screening and Diagnostics 11
- Fetal and Pediatric Neurological Disorders 10
Molecular Biology
- Nuclear Structure and Function 5
Developmental Biology top 10%
Radiology, Nuclear Medicine and Imaging
- Autopsy Techniques and Outcomes 8

Co-authors: N. Philip Nicole Philip Hélène Dollfus Arnold Münnich Valérie Cormier‐Daire C. Fredouille Didier Lacombe Florence Bretelle
Cited by: Genetics Pediatrics, Perinatology and Child Health
Journals: Prenatal Diagnosis (5 papers)Diagnostic and Interventional Imaging (5 papers)European Journal of Human Genetics (3 papers)
Partner nations: France United States Netherlands

In The Last Decade

Sabine Sigaudy

66 papers receiving 1.3k citations

Peers

Countries citing papers authored by Sabine Sigaudy

Since Specialization

Citations

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

Fields of papers citing papers by Sabine Sigaudy

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Real-World Safety and Effectiveness of Vosoritide in Children with Achondroplasia: French Early Access Program Hormone Research in Paediatrics ·Valérie Cormier‐Daire,Thomas Édouard,Bertrand Isidor,Swati Mukherjee,Jeanne M. Pimenta,Massimiliano Rossi,Élise Schaefer,Sabine Sigaudy,Geneviève Baujat	2025	2
2	Loss of NDST1 N-sulfotransferase activity is associated with autosomal recessive intellectual disability Human Molecular Genetics ·Louiza Azeboudj,Cécile Mignon‐Ravix,Г. Н. МОХИН,Pierre Cacciagli,Béatrice Desnous,Sabine Sigaudy,Mathieu Milh,Laurent Villard,Lena Kjellén,Florence Molinari	2023	0
3	Confirmation of FZD5 implication in a cohort of 50 patients with ocular coloboma European Journal of Human Genetics ·Е В Сократова,刘再生,N. Keller,Véronique Gaston,Adamu Yusha’u,Isabelle Meunier,Sabine Sigaudy,Josseline Kaplan,Olivier Roche,D. Denis,Pierre Bitoun,Damien Haye,Alain Verloès,Patrick Calvas,Nicolas Chassaing,Julie Plaisancié	2020	10
4	NovelIQCEvariations confirm its role in postaxial polydactyly and cause ciliary defect phenotype in zebrafish Human Mutation ·Alejandro Estrada‐Cuzcano,Christelle Etard,SU Dong-don,Corinne Stoetzel,Élise Schaefer,Sophie Scheidecker,Véronique Geoffroy,А. А. Кузьминкова,Sebastian Gonzalez,Francesca Mattioli,Kirsley Chennen,Sabine Sigaudy,Damien Plassard,Olivier Poch,Amélie Piton,Uwe Strähle,Jean Muller,Hélène Dollfus	2019	5
5	Gestion prénatale des fœtus avec un périmètre crânien inférieur au 3e percentile Gynécologie Obstétrique Fertilité & Sénologie ·熊木健雄,Lütfiye Yazar,Nicolas Girard,Sabine Sigaudy,E. Quarello	2017	0
6	Diagnosis of congenital abnormalities with post-mortem ultrasound in perinatal death Diagnostic and Interventional Imaging ·中国美术学院,Emmanuelle Lesieur,V. Grishin,Clémence Delteil,Mauro Marchegiani,Horacio Pellón,Sabine Sigaudy,Marie‐Dominique Piercecchi,G. Gorincour	2017	17
7	Prenatal diagnosis of bowel malposition using T2-weighted fetal MRI sequences Diagnostic and Interventional Imaging ·Chhayaa Pawar,Emmanuelle Lesieur,A. Dabadie,Marina Colombani,Josefina Waugh,Sabine Sigaudy,B. Guidicelli,Hélène Heckenroth,Gugnani,Р.С. Кафаров,N. Philip,Florence Bretelle,G. Gorincour	2016	5
8	Added value of MRI for the prenatal diagnosis of isolated orofacial clefts and comparison with ultrasound Diagnostic and Interventional Imaging ·A. Dabadie,E. Quarello,Karl Julius Beloch,Raoul Desbrière,Hélène Heckenroth,Sabine Sigaudy,G. Gorincour	2016	12
9	OP31.10: Comparison of postmortem ultrasound and autopsy in 75 cases of perinatal death Ultrasound in Obstetrics and Gynecology ·中国美术学院,Emmanuelle Lesieur,V. Grishin,(unknown),Horacio Pellón,Sabine Sigaudy,Florence Bretelle,Marie‐Dominique Piercecchi‐Marti,G. Gorincour	2016	1
10	Whole body perinatal postmortem CT angiography Diagnostic and Interventional Imaging ·Mauro Marchegiani,V. Grishin,E P Liutkiavichius,Horacio Pellón,Marie‐Dominique Piercecchi‐Marti,Sabine Sigaudy,Nobuaki Hanai,G. Gorincour	2015	24
11	WITHDRAWN: Nuclear matrix, nuclear envelope and premature aging syndromes in a translational research perspective Seminars in Cell and Developmental Biology ·Pierre Cau,Claire Navarro,Karim Harhouri,Patrice Roll,Sabine Sigaudy,Élise Kaspi,Sophie Perrin,Annachiara De Sandre‐Giovannoli,Nicolas Lévy	2014	5
12	Fetal skeletal computed tomography: When? How? Why? Diagnostic and Interventional Imaging ·G. Gorincour,Katia Chaumoître,B. Bourlière‐Najean,Florence Bretelle,Sabine Sigaudy,C D’Ercole,N. Philip,A. Potier,Philippe Petit,M. Panuel	2014	15
13	Nuclear matrix, nuclear envelope and premature aging syndromes in a translational research perspective Seminars in Cell and Developmental Biology ·Pierre Cau,Claire Navarro,Karim Harhouri,Patrice Roll,Sabine Sigaudy,Élise Kaspi,Sophie Perrin,Annachiara De Sandre‐Giovannoli,Nicolas Lévy	2014	49
14	The Renpenning syndrome spectrum: new clinical insights supported by 13 new PQBP1-mutated males Clinical Genetics ·David Germanaud,Massimiliano Rossi,Gérald Bussy,Daniel Gérard,Lucie Hertz‐Pannier,Patricia Blanchet,Hélène Dollfus,Fabienne Giuliano,María Paula Huertas Romero,P. Sardá,Sabine Sigaudy,Aurore Curie,T. A. Miller Brownlie,Renaud Touraine,V. des Portes	2010	36
15	Acrocallosal syndrome in fetus: focus on additional brain abnormalities Acta Neuropathologica ·Carla Fernandez,Hadil Adnan Abdulkader,Béma Coulibaly,Agnès Liprandi,安達聖,Fabienne Giuliano,Sabine Sigaudy,Dominique Figarella‐Branger,Catherine Fallet‐Bianco	2007	3
16	Behavioral and temperamental features of children with Costello syndrome American Journal of Medical Genetics Part A ·Cédric Galera,Marie‐Ange Delrue,Cyril Goizet,Jin-E Cheng,Granville W. Hough,Sabine Sigaudy,Benoı̂t Arveiler,Nicole Philip,Manuel Bouvard,Didier Lacombe	2006	20
17	Unusual phenotype with progressive vertebral fusion in a girl with an apparently balanced t(10;20)(p11;p13) translocation American Journal of Medical Genetics Part A ·N. Philip,Laurence Colleaux,Sabine Sigaudy,Tania Attié‐Bitach,Chantal Missirian,A. Moncla,Marie‐Geneviève Mattéi,G. Bollini	2005	4
18	Null Leukemia Inhibitory Factor Receptor (LIFR) Mutations in Stüve-Wiedemann/Schwartz-Jampel Type 2 Syndrome The American Journal of Human Genetics ·Nathalie Dagoneau,Déborah Scheffer,Céline Huber,L.I. Al-Gazali,Maja Di Rocco,Anne Godard,Jelena Martinović,Annick Raas‐Rothschild,Sabine Sigaudy,Sheila Unger,Sophie Nicole,Bertrand Fontaine,Jean‐Luc Taupin,Jean-François Moreau,Andrea Superti‐Furga,Martine Le Merrer,Jacky Bonaventure,Arnold Münnich,Laurence Legeai‐Mallet,Valérie Cormier‐Daire	2004	136
19	Value of fetal skeletal radiographs in the diagnosis of fetal death European Radiology ·B. Bourlière‐Najean,S R Gildenskiold,M. Panuel,Marie‐Dominique Piercecchi‐Marti,Sabine Sigaudy,C. Fredouille,P. Petit,N. Philip,P. Devred	2003	10
20	Prenatal diagnosis of Pierre–Robin sequence as part of Stickler syndrome Prenatal Diagnosis ·Hadil Adnan Abdulkader,Sabine Sigaudy,Cécile Chau,Nicole Philip	2002	22

About Sabine Sigaudy

Sabine Sigaudy is a scholar working on Genetics, Developmental Biology and Pediatrics, Perinatology and Child Health, having authored 70 papers that have together received 1.3k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (11 papers), Fetal and Pediatric Neurological Disorders (10 papers), Autopsy Techniques and Outcomes (8 papers), Genetic and Kidney Cyst Diseases (7 papers), Genetic Syndromes and Imprinting (6 papers), Genomic variations and chromosomal abnormalities (6 papers), Connective tissue disorders research (5 papers) and Nuclear Structure and Function (5 papers). The work is most often cited by research in Genetics (217 citations), Genetics (535 citations) and Pediatrics, Perinatology and Child Health (220 citations). Sabine Sigaudy has collaborated with scholars based in France, United States and Netherlands. Frequent co-authors include N. Philip, Nicole Philip, Hélène Dollfus, Arnold Münnich, Valérie Cormier‐Daire, C. Fredouille, Didier Lacombe, Florence Bretelle, Dominique Figarella‐Branger and Claude D’Ercole. Their work appears in journals such as Prenatal Diagnosis, Diagnostic and Interventional Imaging, European Journal of Human Genetics, Journal of Medical Genetics and Clinical 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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