N. Morichon-Delvallez

1.2k total citations
26 papers, 418 citations indexed

About

N. Morichon-Delvallez is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, N. Morichon-Delvallez has authored 26 papers receiving a total of 418 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 14 papers in Pediatrics, Perinatology and Child Health and 12 papers in Molecular Biology. Recurrent topics in N. Morichon-Delvallez's work include Genomic variations and chromosomal abnormalities (17 papers), Prenatal Screening and Diagnostics (14 papers) and Genetic Syndromes and Imprinting (5 papers). N. Morichon-Delvallez is often cited by papers focused on Genomic variations and chromosomal abnormalities (17 papers), Prenatal Screening and Diagnostics (14 papers) and Genetic Syndromes and Imprinting (5 papers). N. Morichon-Delvallez collaborates with scholars based in France and United States. N. Morichon-Delvallez's co-authors include Michel Vekemans, J Couturier, Arnold Münnich, Bernard Dutrillaux, C Turleau, Anne‐Lise Delezoide, Laurence Faivre, Géraldine Viot, Damien Sanlaville and Valérie Raclin and has published in prestigious journals such as The American Journal of Human Genetics, Human Reproduction and Journal of Medical Genetics.

In The Last Decade

N. Morichon-Delvallez

26 papers receiving 366 citations

Peers

Countries citing papers authored by N. Morichon-Delvallez

Since Specialization

Citations

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

Fields of papers citing papers by N. Morichon-Delvallez

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by N. Morichon-Delvallez. 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 N. Morichon-Delvallez. The network helps show where N. Morichon-Delvallez may publish in the future.

Co-authorship network of co-authors of N. Morichon-Delvallez

This figure shows the co-authorship network connecting the top 25 collaborators of N. Morichon-Delvallez. A scholar is included among the top collaborators of N. Morichon-Delvallez 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 N. Morichon-Delvallez. N. Morichon-Delvallez 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	Array-based comparative genomic hybridization identifies a high frequency of copy number variations in patients with syndromic overgrowth 2009 ·European Journal of Human Genetics ·Valérie Malan, (unknown), Gwendoline Soler, Christine Coubes, Didier Lacombe, Laurent Pasquier, Jean Soulier, N. Morichon-Delvallez, C Turleau, Arnold Münnich, Serge Romana, Michel Vekemans, Valérie Cormier‐Daire, Laurence Colleaux	12
2	Maternal uniparental heterodisomy of chromosome 17 in a patient with nephropathic cystinosis 2009 ·European Journal of Human Genetics ·Anne-Sophie Lèbre, Vincent Morinière, Olivier Dunand, A Bensman, N. Morichon-Delvallez, Corinne Antignac	20
3	Familial interstitial Xq27.3q28 duplication encompassing the FMR1 gene but not the MECP2 gene causes a new syndromic mental retardation condition 2009 ·European Journal of Human Genetics ·Marlène Rio, Valérie Malan, Sarah Boissel, Annick Toutain, (unknown), Stéphanie Gobin, N. Morichon-Delvallez, C Turleau, Jean‐Paul Bonnefont, Arnold Münnich, Michel Vekemans, Laurence Colleaux	29
4	Prenatal diagnosis of a ring chromosome 14 in a fetus with a severe skeletal dysplasia 2008 ·Prenatal Diagnosis ·(unknown), Valérie Malan, Jelena Martinović, Férechté Encha‐Razavi, Bernard Aral, Isabelle Texier, Jean‐Paul Bonnefont, Michel Vekemans, N. Morichon-Delvallez	2
5	Prenatal diagnosis and normal outcome of a 46,XX/46,XY chimera: A Case Report 2007 ·Human Reproduction ·Valérie Malan, (unknown), N. Morichon-Delvallez, (unknown), Alexandra Benachi, Damien Sanlaville, C Turleau, Jean‐Paul Bonnefont, (unknown), Michel Vekemans	32
6	Cytogenetic and histological features of a human embryo with homogeneous chromosome 8 trisomy 2006 ·Prenatal Diagnosis ·Christelle Golzio, (unknown), Catherine Ozilou, Sophie Thomas, Géraldine Goudefroye, N. Morichon-Delvallez, Michel Vekemans, Tania Attié‐Bitach, Heather Etchevers	17
7	Molecular characterisation of a prenatally diagnosed 5q15q21.3 deletion and review of the literature 2006 ·Prenatal Diagnosis ·Valérie Malan, Jelena Martinović, Damien Sanlaville, (unknown), (unknown), (unknown), Julia Tantau, Tania Attié‐Bitach, Michel Vekemans, N. Morichon-Delvallez	7
8	Anomalies chromosomiques 2006 ·(unknown), N. Morichon-Delvallez	1
9	Functional disomy of the Xq28 chromosome region 2005 ·European Journal of Human Genetics ·Damien Sanlaville, Marguerite Prieur, Marie‐Christine de Blois, David Geneviève, (unknown), Catherine Ozilou, (unknown), Philippe Gosset, N. Morichon-Delvallez, Arnold Münnich, Valérie Cormier‐Daire, Geneviève Baujat, Serge Romana, Michel Vekemans, C Turleau	63
10	Molecular screening of the ZFHX1B gene in prenatally diagnosed isolated agenesis of the corpus callosum 2004 ·Prenatal Diagnosis ·Yolanda Espinosa‐Parrilla, Férechté Encha‐Razavi, Tania Attié‐Bitach, Jelena Martinović, N. Morichon-Delvallez, Arnold Münnich, Michel Vekemans, Stanislas Lyonnet, Jeanne Amiel	6
11	Subtle familial unbalanced translocation t(8;11)(p23.2;p15.5) in two fetuses with Beckwith-Wiedemann features 2000 ·Prenatal Diagnosis ·Sandra Fert‐Ferrer, (unknown), Julia Tantau, Anne Lise Delezoïde, Catherine Ozilou, Serge Romana, Philippe Gosset, (unknown), (unknown), Claude Moraine, N. Morichon-Delvallez, C Turleau, Michel Vekemans, Marguerite Prieur	10
12	Prenatal detection of a 1p36 deletion in a fetus with multiple malformations and a review of the literature 1999 ·Prenatal Diagnosis ·Laurence Faivre, N. Morichon-Delvallez, Géraldine Viot, Jelena Martinović, (unknown), J. P. Aubry, Valérie Raclin, Patrick Edery, Yves Dumez, Arnold Münnich, Michel Vekemans	32
13	Prenatal diagnosis of an 8p23.1 deletion in a fetus with a diaphragmatic hernia and review of the literature 1998 ·Prenatal Diagnosis ·Laurence Faivre, N. Morichon-Delvallez, Géraldine Viot, Françoise Narcy, (unknown), Laurent Mandelbrot, M. C. Aubry, Valérie Raclin, Patrick Edery, Arnold Münnich, Michel Vekemans	41
14	Molecular cytogenetic analysis of patients with holoprosencephaly and structural rearrangements of 7q. 1998 ·PubMed ·Gail H. Vance, Cheryl A. Nickerson, (unknown), Aijun Zhang, Octavian Henegariu, N. Morichon-Delvallez, Merlin G. Butler, Catherine G. Palmer	8
15	First-Trimester Translucency: Aneuploidy, Sonographic Findings, and Maternal Age 1996 ·Fetal Diagnosis and Therapy ·D. Mahieu‐Caputo, Marc Dommergues, N. Morichon-Delvallez, M. C. Aubry, (unknown), Yves Dumez	4
16	Maternal uniparental disomy for chromosome 14 by secondary nondisjunction of a initial trisomy 1994 ·The American Journal of Human Genetics ·N. Morichon-Delvallez, (unknown), (unknown)	12
17	Holoprosencephaly and sacral agenesis in a fetus with a terminal deletion 7q36-->7qter. 1993 ·Journal of Medical Genetics ·N. Morichon-Delvallez, Anne‐Lise Delezoide, Michel Vekemans	30
18	[Paracentric inversion: a study of 2 new cases]. 1985 ·PubMed ·N. Morichon-Delvallez, (unknown)	2
19	[Paracentric inversions in man. Apropos of 2 familial observations]. 1985 ·PubMed ·N. Morichon-Delvallez, (unknown)	3
20	[Attenuated phenotype of trisomy 4p by translocation t(X;4)(p21.2;p13)]. 1982 ·PubMed ·N. Morichon-Delvallez, J Couturier, (unknown)	4

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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