D. Molina Gomes

1.6k citations

24 papers · 789 indexed · h-index 15

Molecular Biology
Genetics top 5%
Pediatrics, Perinatology and Child Health top 5%
Public Health, Environmental and Occupational Health top 10%
Reproductive Medicine top 5%

Co-authors: Déborah Bourc’his E. Viégas-Pèquignot Alain Niveleau M Plachot Andràs Páldi Nathalie Rougier François Vialard J. Selva
Topics: Prenatal Screening and Diagnostics (15 papers)Genomic variations and chromosomal abnormalities (7 papers)Chromosomal and Genetic Variations (6 papers)
Cited by: Pediatrics, Perinatology and Child Health Genetics Reproductive Medicine
Journals: Genes & Development Human Reproduction Fertility and Sterility
Partner nations: France Italy Australia

In The Last Decade

D. Molina Gomes

24 papers receiving 733 citations

Peers

Countries citing papers authored by D. Molina Gomes

Since Specialization

Citations

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

Fields of papers citing papers by D. Molina Gomes

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by D. Molina Gomes. 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 D. Molina Gomes. The network helps show where D. Molina Gomes may publish in the future.

Co-authorship network of co-authors of D. Molina Gomes

This figure shows the co-authorship network connecting the top 25 collaborators of D. Molina Gomes. A scholar is included among the top collaborators of D. Molina Gomes 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 D. Molina Gomes. D. Molina Gomes 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	Étude des aspects psychologiques des fausses couches à répétition à l’aide d’un questionnaire de personnalité approfondi : le MMPI-2 2013 ·Gynécologie Obstétrique & Fertilité ·(unknown),(unknown),(unknown),(unknown),D. Molina Gomes,(unknown),(unknown)	1
2	The High Frequency of Sperm Aneuploidy in Klinefelter Patients and in Nonobstructive Azoospermia Is Due to Meiotic Errors in Euploid Spermatocytes 2012 ·Journal of Andrology ·François Vialard,M. Bailly,(unknown),Martine Albert,(unknown),(unknown),Marianne Bergère,D. Molina Gomes,Philippe de Mazancourt,J. Selva	29
3	Follicular fluid protein content (FSH, LH, PG4, E2 and AMH) and polar body aneuploidy 2012 ·Journal of Assisted Reproduction and Genetics ·Ibrahim Hammoud,François Vialard,Marianne Bergère,Martine Albert,D. Molina Gomes,(unknown),(unknown),M. Bailly,Robert Wainer,J. Selva	10
4	Can one translocation impact the meiotic segregation of another translocation? A sperm-FISH analysis of a 46,XY,t(1;16)(q21;p11.2),t(8;9) (q24.3;p24) patient and his 46,XY,t(8;9)(q24.3;p24) brother and cousin 2012 ·Molecular Human Reproduction ·F. Ferfouri,Florence Boitrelle,Patrice Clément,D. Molina Gomes,J. Selva,François Vialard	5
5	Prenatal BACs‐on‐Beads^TM: the prospective experience of five prenatal diagnosis laboratories 2012 ·Prenatal Diagnosis ·François Vialard,Giuseppe Simoni,D. Molina Gomes,(unknown),Simona De Toffol,(unknown),(unknown),Lucio Nitsch,P. Bouhanna,(unknown),Thomas Popowski,Beatrice Grimi,José Antonio Martínez-Conejero,Brigitte Benzacken,Rita Genesio,Francesca Romana Grati	35
6	Application of a new molecular technique for the genetic evaluation of products of conception 2012 ·Prenatal Diagnosis ·Francesca Romana Grati,D. Molina Gomes,Devika Ganesamoorthy,(unknown),Simona De Toffol,(unknown),Francesca Malvestiti,Laurence Lœuillet,Anna Ruggeri,Robert Wainer,Federico Maggi,Azzedine Aboura,Céline Dupont,Anne Claude Tabet,Fabien Guimiot,Howard R. Slater,Giuseppe Simoni,François Vialard	15
7	The chromosomal risk in sperm from heterozygous Robertsonian translocation carriers is related to the sperm count and the translocation type 2011 ·Fertility and Sterility ·F. Ferfouri,J. Selva,Florence Boitrelle,D. Molina Gomes,Antoine Torre,Martine Albert,M. Bailly,Patrice Clément,François Vialard	23
8	Sperm FISH analysis of a 46,XY,t(3;6)(p24;p21.2),inv (8)(p11;2q21.2) double chromosomal rearrangement 2011 ·Reproductive BioMedicine Online ·F. Ferfouri,Florence Boitrelle,(unknown),D. Molina Gomes,J. Selva,François Vialard	6
9	Prise en charge psychologique des échecs de procréation, au masculin : une blessure peut en cacher une autre 2009 ·Gynécologie Obstétrique & Fertilité ·(unknown),D. Molina Gomes,Martine Albert,M. Bailly,Marianne Bergère,J. Selva	4
10	Array Comparative Genomic Hybridization in Prenatal Diagnosis: Another Experience 2009 ·Fetal Diagnosis and Therapy ·François Vialard,D. Molina Gomes,Bonnie S. LeRoy,E. Quarello,(unknown),(unknown),Valérie Serazin,J. Roume,Y. Ville,Philippe de Mazancourt,J. Selva	60
11	Meiotic segregation of X-autosome translocation in two carriers and implications for assisted reproduction 2009 ·Reproductive BioMedicine Online ·Aurore Perrin,François Vialard,Nathalie Douet‐Guilbert,D. Molina Gomes,(unknown),Marc De Braekeleer,J. Selva	18
12	Sperm chromosome analysis of an infertile patient with a 95% mosaic r(21) karyotype and normal phenotype 2009 ·Fertility and Sterility ·Ibrahim Hammoud,D. Molina Gomes,Marianne Bergère,Robert Wainer,J. Selva,François Vialard	24
13	Is classic pericentric inversion of chromosome 2 inv(2)(p11q13) associated with an increased risk of unbalanced chromosomes? 2009 ·Fertility and Sterility ·F. Ferfouri,Patrice Clément,D. Molina Gomes,(unknown),Edouard Amar,J. Selva,François Vialard	27
14	Oocyte aneuploidy mechanisms are different in two situations of increased chromosomal risk: older patients and patients with recurrent implantation failure after in vitro fertilization 2007 ·Fertility and Sterility ·François Vialard,Raoul Lombroso,Marianne Bergère,D. Molina Gomes,Ibrahim Hammoud,M. Bailly,J. Selva	20
15	Evidence of a high proportion of premature unbalanced separation of sister chromatids in the first polar bodies of women of advanced age 2006 ·Human Reproduction ·François Vialard,Christine Petit,Marianne Bergère,D. Molina Gomes,(unknown),Raoul Lombroso,Y. Ville,H Gérard,J. Selva	41
16	Prenatal diagnosis of de novo (7;19)(q11.2;q13.3) translocation associated with a thick corpus callosum and Wilms tumor of the kidneys 2005 ·Prenatal Diagnosis ·O. Cavicchioni,D. Molina Gomes,Brigitte Leroy,François Vialard,Y. Hillion,J. Selva,Y. Ville	9
17	Fetal karyotyping after 28 weeks of gestation for late ultrasound findings in a low risk population 2003 ·Prenatal Diagnosis ·(unknown),D. Molina Gomes,Marie‐Victoire Sénat,François Audibert,(unknown),Y. Ville	23
18	Abnormal methylation does not prevent X inactivation in ICF patients 1999 ·Cytogenetic and Genome Research ·Déborah Bourc’his,Pierre Miniou,Marc Jeanpierre,D. Molina Gomes,Jean‐Michel Dupont,Geneviève de Saint Basile,P Maraschio,L. Tiepolo,E. Viégas-Pèquignot	32
19	Chromosome methylation patterns during mammalian preimplantation development 1998 ·Genes & Development ·Nathalie Rougier,Déborah Bourc’his,D. Molina Gomes,Alain Niveleau,M Plachot,Andràs Páldi,E. Viégas-Pèquignot	335
20	Undermethylation of Alu sequences in ICF syndrome: molecular and in situ analysis 1997 ·Cytogenetic and Genome Research ·Pierre Miniou,Déborah Bourc’his,D. Molina Gomes,Marc Jeanpierre,E. Viégas-Pèquignot	31

About D. Molina Gomes

D. Molina Gomes is a scholar working on Pediatrics, Perinatology and Child Health, Reproductive Medicine and Genetics, having authored 24 papers that have together received 789 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (15 papers), Genomic variations and chromosomal abnormalities (7 papers) and Chromosomal and Genetic Variations (6 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (348 citations), Genetics (428 citations) and Reproductive Medicine (100 citations). D. Molina Gomes has collaborated with scholars based in France, Italy and Australia. Frequent co-authors include Déborah Bourc’his, E. Viégas-Pèquignot, Alain Niveleau, M Plachot, Andràs Páldi, Nathalie Rougier, François Vialard, J. Selva, Marianne Bergère and Y. Ville. Their work appears in journals such as Genes & Development, Human Reproduction and Fertility and Sterility.

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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