N. Morichon-Delvallez

1.2k citations
26 papers · 418 indexed · h-index 12
Topics
Genomic variations and chromosomal abnormalities (17 papers)Prenatal Screening and Diagnostics (14 papers)Genetic Syndromes and Imprinting (5 papers)
Partner nations
FranceUnited States

In The Last Decade

N. Morichon-Delvallez

26 papers receiving 366 citations

Peers

N. Morichon-Delvallez
Comparison fields: 5 of 37
  • Genetics 320
  • Molecular Biology 173
  • Pediatrics, Perinatology and Child Health 143
  • Plant Science 74
  • Surgery 66
Replace Drew Duckett with:
Drew Duckett United Kingdom
Sandra Peacock United States
Roberto Coco Argentina
Winnie Courtens Belgium
Nathalie Leporrier France
M. Barr United States
Anne M. Bandholz United States
Fernando Santos Spain
Beth A. Torchia United States
Amelia Villa Spain
N. Morichon-Delvallez relative to Drew Duckett United Kingdom Drew Duckett's profile →
Citations per field
00.5×
Drew Duckett · 1×
Citations per year

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

20 of 20 papers shown
#WorkIndexed citations
1 12
2 20
3 29
4 2
5 32
6 17
7 7
8 1
9 63
10 6
11 10
12 32
13 41
14
Molecular cytogenetic analysis of patients with holoprosencephaly and structural rearrangements of 7q.
8
15 4
16
Maternal uniparental disomy for chromosome 14 by secondary nondisjunction of a initial trisomy
12
17 30
18
[Paracentric inversion: a study of 2 new cases].
2
19
[Paracentric inversions in man. Apropos of 2 familial observations].
3
20
[Attenuated phenotype of trisomy 4p by translocation t(X;4)(p21.2;p13)].
4

About N. Morichon-Delvallez

N. Morichon-Delvallez is a scholar working on Developmental Biology, Genetics and Pediatrics, Perinatology and Child Health, having authored 26 papers that have together received 418 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (17 papers), Prenatal Screening and Diagnostics (14 papers) and Genetic Syndromes and Imprinting (5 papers). The work is most often cited by research in Genetics (320 citations), Pediatrics, Perinatology and Child Health (143 citations) and Developmental Biology (11 citations). N. Morichon-Delvallez has collaborated with scholars based in France and United States. Frequent 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. Their work appears in journals such as The American Journal of Human Genetics, Human Reproduction and Journal of Medical 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026