Marion Gérard‐Blanluet

752 citations

24 papers · 399 indexed · h-index 13

Genetics
- Genomic variations and chromosomal abnormalities 5
- Genetic and Kidney Cyst Diseases 4
- Genetic Syndromes and Imprinting 3
- Congenital Ear and Nasal Anomalies 3
Pediatrics, Perinatology and Child Health
- Prenatal Screening and Diagnostics 5
Urology
- Urological Disorders and Treatments 3
Clinical Biochemistry
Genetics
- Genomic variations and chromosomal abnormalities 5
- Genetic and Kidney Cyst Diseases 4
- Genetic Syndromes and Imprinting 3
- Congenital Ear and Nasal Anomalies 3
Plant Science
- Chromosomal and Genetic Variations 3
Pathology and Forensic Medicine
- Tumors and Oncological Cases 3

Co-authors: Alain Verloès Sandra P. Reyna Francis Renault Kenneth Silver Matthew Sweney Alexis Arzimanoglou Kathryn J. Swoboda Aga Lewelt
Cited by: Genetics Pediatrics, Perinatology and Child Health Urology
Journals: Prenatal Diagnosis (4 papers)American Journal of Medical Genetics Part A (9 papers)Annals of the Rheumatic Diseases (1 paper)
Partner nations: France United States Denmark

In The Last Decade

Marion Gérard‐Blanluet

24 papers receiving 388 citations

Peers

Countries citing papers authored by Marion Gérard‐Blanluet

Since Specialization

Citations

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

Fields of papers citing papers by Marion Gérard‐Blanluet

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marion Gérard‐Blanluet. 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 Marion Gérard‐Blanluet. The network helps show where Marion Gérard‐Blanluet may publish in the future.

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	High-functioning autism spectrum disorder and fragile X syndrome: report of two affected sisters Molecular Autism ·Pauline Chaste,Catalina Betancur,Marion Gérard‐Blanluet,Eka Devia Ayuningtyas,Bradley C. Stillman,Séverine Drunat,Marion Leboyer,Thomas Bourgeron,Richard Delorme	2012	12
2	Aphallia, Lung Agenesis and Multiple Defects of Blastogenesis Fetal and Pediatric Pathology ·Marion Gérard‐Blanluet,Véronique Lambert,Suonavy Khung‐Savatovsky,Catherine Robinson,Sandrine Passemard,Clarisse Baumann,Anne‐Lise Delezoide,Alain Verloès	2011	9
3	Binder phenotype in mothers affected with autoimmune disorders The Journal of Maternal-Fetal & Neonatal Medicine ·Estelle Colin,Renaud Touraine,J.‐M. Levaillant,Laurent Pasquier,F. Boussion,Bal K. Jerath,Agnès Guichet,M. Barth,J. Day,Marion Gérard‐Blanluet,Sylvie Odent,Dominique Bonneau	2011	11
4	Unilateral agenesis of the abdominal wall musculature: An early muscle deficiency American Journal of Medical Genetics Part A ·Marion Gérard‐Blanluet,L. Racca,Clarisse Baumann,Catherine Robinson,何兴华,G. Audry,Anne‐Lise Delezoide,Alain Verloès	2010	5
5	Binder phenotype: clinical and etiological heterogeneity of the so‐called Binder maxillonasal dysplasia in prenatally diagnosed cases, and review of the literature Prenatal Diagnosis ·J. M. Levaillant,S. Yannal,Larissa Barbosa Silva,Martine Bucourt,Lydie Bürglen,V. Soupre,Clarisse Baumann,Cyrus Gerami,Renaud Touraine,Arnaud Picard,E. Vuillard,N. Belarbi,J.F. Oury,Alain Verloès,M.-P. Vazquez,Philippe Labrune,Anne‐Lise Delezoide,Marion Gérard‐Blanluet	2009	24
6	Partial trisomy of chromosome 22 resulting from a supernumerary marker chromosome 22 in a child with features of cat eye syndrome American Journal of Medical Genetics Part A ·Åsa Tellgren,Marion Gérard‐Blanluet,Stéphane Serero,杨玉慧,Clarisse Baumann,Marie‐Line Jacquemont,Céline Dupont,Lin Rui-guo,Séverine Drunat,雅文関根,Nicola Kingston,Brigitte Benzacken,Alain Verloès,Anne‐Claude Tabet,Azzedine Aboura	2008	9
7	CEMARA: a Web dynamic application within a N-tier architecture for rare diseases. PubMed ·Claude Messiaen,Loïc Le Mignot,Ana Rath,Jean‐Baptiste Richard,Éric Dufour,Mohamed Said,F. Cunsolo,Alain Verloès,Martine Le Merrer,Christine Bodemer,Geneviève Baujat,Marion Gérard‐Blanluet,E. Bourdon‐Lanoy,Rémi Salomon,Ségolène Aymé,Paul Landais	2008	18
8	De novo Subtelomeric Deletion Additional to an Inherited Apparently Balanced Reciprocal Translocation Fetal Diagnosis and Therapy ·(unknown),Eva Pipiras,Patricia Plaut,Cyril Touboul,Daniel Daghbas,Férechté Encha‐Razavi,Roope Koponen,Moncef Benkhalifa,R Fehr,Stéphane Serero,Jean‐Philippe Wolf,Marion Gérard‐Blanluet,Brigitte Benzacken	2007	3
9	CNS malformations in Knobloch syndrome with splice mutation in COL18A1 gene American Journal of Medical Genetics Part A ·Boris Keren,Oscar Suzuki,Marion Gérard‐Blanluet,Dominique Brémond‐Gignac,Monique Elmaleh,Luigi Titomanlio,Anne‐Lise Delezoide,Maria Rita Passos‐Bueno,Alain Verloès	2007	31
10	Specific osseous spurs in a lethal form of hypophosphatasia correlated with 3D prenatal ultrasonographic images Prenatal Diagnosis ·Roope Koponen,J. M. Levaillant,Daniel Daghbas,Stéphane Mimouni,Férechté Encha‐Razavi,Étienne Mornet,M. Le Merrer,Marion Gérard‐Blanluet	2007	17
11	Recurrent insertional polydactyly and situs inversus in a Bardet‐Biedl syndrome family American Journal of Medical Genetics Part A ·Christine Deffert,Florence Niel,Fanny Mochel,Catherine Barrey,C. Romaña,Eric H. Souied,Corinne Stoetzel,Michel Goossens,Hélène Dollfus,Alain Verloès,Emmanuelle Girodon,Marion Gérard‐Blanluet	2006	6
12	Bilateral periventricular heterotopias in an X‐linked dominant transmission in a family with two affected males American Journal of Medical Genetics Part A ·Marion Gérard‐Blanluet,Volney Sheen,P. Gudermuth,Jason Neal,Kira Apse,Claude Danan,Martine Sinico,Pierre Brugières,N. D. (Nguyen) Bieu,励吉村,雅文関根,Nicola Kingston,Serge Amselem,Christopher A. Walsh,Férechté Encha‐Razavi	2006	20
13	Intrafamilial segregation analysis of the p.E148Q MEFV allele in familial Mediterranean fever Annals of the Rheumatic Diseases ·Dimitri Tchernitchko,Marion Gérard‐Blanluet,Marie Legendre,C. Cazeneuve,Gilles Grateau,Serge Amselem	2006	19
14	Prenatal phenotypic overlap of Costello syndrome and severe Noonan syndrome by tri‐dimensional ultrasonography Prenatal Diagnosis ·Aparna Calderón,Marion Gérard‐Blanluet,Muriel Holder‐Espinasse,万文革,Louise Devisme,Hélène Cavé,Sylvie Manouvrier‐Hanu	2006	19
15	Three patients with hallucal polydactyly and WAGR syndrome, including discordant expression of Wilms tumor in MZ twins American Journal of Medical Genetics Part A ·Dominique Brémond‐Gignac,Marion Gérard‐Blanluet,Henri Copin,Pierre Bitoun,Clarisse Baumann,John A. Crolla,Brigitte Benzacken,Alain Verloès	2005	13
16	Prenatal forehead edema in 4p- deletion: the ‘Greek warrior helmet’ profile revisited Prenatal Diagnosis ·J. M. Levaillant,Cyril Touboul,Roope Koponen,Daniel Daghbas,Stéphane Serero,Fang Yuanlin,Stéphane Mimouni,Issam Abd Alsamad,陈跃鑫,Marion Gérard‐Blanluet	2005	15
17	Giant omphalocele and “prune belly” sequence as components of the Beckwith–Wiedemann syndrome American Journal of Medical Genetics Part A ·Martine Sinico,Claudine Touboul,Bassam Haddad,Férechté Encha‐Razavi,J R A Miranda,Christine Gicquel,Marion Gérard‐Blanluet	2004	12
18	Classical West “syndrome” phenotype with a subtelomeric 4p trisomy American Journal of Medical Genetics Part A ·Marion Gérard‐Blanluet,Serge Romana,孫小玉,Marc Le Lorc’h,Patricia Plaut,Roope Koponen,Cyril Touboul,J. M. Levaillant,Bassam Haddad,Joseph G. Palmer,F. Lelong,Thierry Billette de Villemeur,Alain Verloès,中田邦博	2004	10
19	Mosaic trisomy 9 and lobar holoprosencephaly American Journal of Medical Genetics ·Marion Gérard‐Blanluet,Claude Danan,Martine Sinico,F. Lelong,中田邦博,Gilles Dassieu,Nicola Kingston,Sylvie Odent,Férechté Encha‐Razavi	2002	12
20	Mosaic trisomy 15 and hemihypertrophy Annales de Génétique ·Marion Gérard‐Blanluet,雅文関根,Anne Bazin,Claude Danan,Alain Verloès,Nicola Kingston	2001	5

About Marion Gérard‐Blanluet

Marion Gérard‐Blanluet is a scholar working on Genetics, Urology, Pediatrics, Perinatology and Child Health, Genetics and Pathology and Forensic Medicine, having authored 24 papers that have together received 399 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (5 papers), Genetic and Kidney Cyst Diseases (4 papers), Genetic Syndromes and Imprinting (3 papers), Urological Disorders and Treatments (3 papers), Chromosomal and Genetic Variations (3 papers), Congenital Ear and Nasal Anomalies (3 papers) and Tumors and Oncological Cases (3 papers). The work is most often cited by research in Genetics (158 citations), Pediatrics, Perinatology and Child Health (72 citations), Urology (22 citations), Clinical Biochemistry (22 citations) and Genetics (31 citations). Marion Gérard‐Blanluet has collaborated with scholars based in France, United States and Denmark. Frequent co-authors include Alain Verloès, Sandra P. Reyna, Francis Renault, Kenneth Silver, Matthew Sweney, Alexis Arzimanoglou, Kathryn J. Swoboda, Aga Lewelt, Férechté Encha‐Razavi and Anne‐Lise Delezoide. Their work appears in journals such as Prenatal Diagnosis, American Journal of Medical Genetics Part A, Annals of the Rheumatic Diseases, PEDIATRICS and Fetal Diagnosis and Therapy.

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