Stéphane Serero

481 citations

15 papers · 328 indexed · h-index 8

Impact in

Reproductive Medicine top 10%
- Ovarian function and disorders
Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Papers in

Pediatrics, Perinatology and Child Health 11
- Prenatal Screening and Diagnostics 11
- Fetal and Pediatric Neurological Disorders 3
- Assisted Reproductive Technology and Twin Pregnancy 1
Genetics 8
- Genomic variations and chromosomal abnormalities 7
- Genetic Syndromes and Imprinting 1

Co-authors: J Frézal N. Van Cong Odile Cohen‐Haguenauer Nathalie Josso M.-F. de Tand Jean‐Yves Picard M. C. Hors‐Cayla Marie‐Geneviève Mattéi
Journals: Prenatal Diagnosis (4 papers)Fetal Diagnosis and Therapy (2 papers)Human Genetics (2 papers)Frontiers in Genetics (1 paper)Cytogenetic and Genome Research (1 paper)
Partner nations: France United States Canada

In The Last Decade

Stéphane Serero

13 papers receiving 300 citations

Peers

Countries citing papers authored by Stéphane Serero

Since Specialization

Citations

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

Fields of papers citing papers by Stéphane Serero

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

Sort: Min cites: Since: Top N: Style:

15 of 15 papers shown

#	Work
1	Case Report: How whole-genome sequencing-based cell-free DNA prenatal testing can help identify a marker mhromosome Frontiers in Genetics ·Pascale Kleinfinger, İlknur Güneştaş, Armelle Luscan, Detlef Trost, Mirko Cvijan, Mylène Valduga, Stéphane Serero, Jean‐Marc Costa, T kodama	2022	0
2	Noninvasive Prenatal Screening for Trisomy 21 in Patients with a Vanishing Twin Genes ·Pascale Kleinfinger, Armelle Luscan, Verónica Carrero-Segura, Rodziah Mat Selimin, Mirko Cvijan, Stéphane Serero, Mylène Valduga, Detlef Trost, Jean‐Marc Costa, Alexandre Vivanti, T kodama	2022	5
3	Trisomy 13 by robertsonian translocation rob (13;13)(q10;q10) +13: about one case Annales de biologie clinique ·Antoine Laudat, Stéphane Serero, Hastings Okoth Ogendo, Eglis González	2017	0
4	Pre‐ and postnatal phenotype of 6p25 deletions involving the FOXC1 gene American Journal of Medical Genetics Part A ·Andrée Delahaye‐Duriez, Suonavy Khung‐Savatovsky, Azzedine Aboura, Fabien Guimiot, Séverine Drunat, Jean‐Luc Alessandri, Marion Gérard, Pierre Bitoun, 甚一尾花, Stéphanie Robin, C. Huel, Margarida Maria Baptista Mendes Pedroso de Lima, Stéphane Serero, Pierre Gressèns, Jacques Élion, Alain Verloès, Brigitte Benzacken, Anne‐Lise Delezoide, Eva Pipiras	2012	37
5	Prenatal BACs‐on‐Beads^™: a new technology for rapid detection of aneuploidies and microdeletions in prenatal diagnosis Prenatal Diagnosis ·François Vialard, Giuseppe Simoni, Azzedine Aboura, Simona De Toffol, 国雄牛場, Lene Kromann, Stéphane Serero, Patrice Clément, P. Bouhanna, Étienne Rouleau, Beatrice Grimi, J. Selva, Elisa Gaetani, Federico Maggi, マーガレットアトウッド, Brigitte Benzacken, Francesca Romana Grati	2011	40
6	Fluorescence in situ hybridization in prenatal screening: lessons from an inherited chromosome 18 marker Prenatal Diagnosis ·M. Valentin, E. Bettoni, Stéphane Serero, Françoise Müller, Dominique Luton, Guillaume Ducarme	2009	1
7	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
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	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
10	Isolated Fetal Hyperechogenic Bowel Associated with Intra-Uterine Parvovirus B19 Infection Fetal Diagnosis and Therapy ·Manuel Marquès, Laurent Gavard, Cai Zi, Françoise Müller, Stéphane Serero, Jean‐Louis Bénifla, Jean-Marc Costa	2005	5
11	Evaluation of X, Y, 18, and 13/21 alpha satellite DNA probes for interphase cytogenetic analysis of uncultured amniocytes by fluorescencein situhybridization Prenatal Diagnosis ·V. Cacheux, Gérard Tachdjian, Fang Yuanlin, J.-F. Oury, Stéphane Serero, Philippe Blot, C Nessmann	1994	37
12	Regional mapping of the human renin gene to 1q32 by in situ hybridization. PubMed ·Odile Cohen‐Haguenauer, Florent Soubrier, N. Van Cong, Stéphane Serero, C Turleau, Gunnbjørg Tysvær, Marie‐Sylvie Gross, Pierre Corvol, J Frézal	1989	11
13	Localization of the active gene of aldolase on chromosome 16, and two aldolase A pseudogenes on chromosomes 3 and 10 Human Genetics ·Stéphane Serero, Pascal Maire, N. Van Cong, Odile Cohen‐Haguenauer, Marie‐Sylvie Gross, D. van der Meulen, M.-F. de Tand, A Kahn, J Frézal	1988	6
14	Assignment of the human fast skeletal muscle myosin alkali light chains gene (MLC1F/MLC3F) to 2q 32.1-2qter Human Genetics ·Odile Cohen‐Haguenauer, Paul J.R. Barton, N. Van Cong, Stéphane Serero, Marie‐Sylvie Gross, D. van der Meulen, Tovo Hanitra RATOVOHAJA, Benoît Robert, Margaret Buckingham, J Frézal	1988	13
15	Mapping of the gene for anti-Müllerian hormone to the short arm of human chromosome 19 Cytogenetic and Genome Research ·Odile Cohen‐Haguenauer, Jean‐Yves Picard, Marie‐Geneviève Mattéi, Stéphane Serero, N. Van Cong, M.-F. de Tand, Daniel Guerrier, M. C. Hors‐Cayla, Nathalie Josso, J Frézal	1987	146

About Stéphane Serero

Stéphane Serero is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Pathology and Forensic Medicine, Obstetrics and Gynecology and Reproductive Medicine, having authored 15 papers that have together received 328 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (11 papers), Genomic variations and chromosomal abnormalities (7 papers), Tumors and Oncological Cases (3 papers), Fetal and Pediatric Neurological Disorders (3 papers), Chromosomal and Genetic Variations (3 papers), Genetic Syndromes and Imprinting (1 paper), Assisted Reproductive Technology and Twin Pregnancy (1 paper) and Pregnancy and preeclampsia studies (1 paper). The work is most often cited by research in Reproductive Medicine (62 citations), Genetics (188 citations), Pediatrics, Perinatology and Child Health (110 citations), Urology (24 citations) and Rheumatology (35 citations). Stéphane Serero has collaborated with scholars based in France, United States and Canada. Frequent co-authors include J Frézal, N. Van Cong, Odile Cohen‐Haguenauer, Nathalie Josso, M.-F. de Tand, Jean‐Yves Picard, M. C. Hors‐Cayla, Marie‐Geneviève Mattéi, Daniel Guerrier and Philippe Blot. Their work appears in journals such as Prenatal Diagnosis, Fetal Diagnosis and Therapy, Human Genetics, Frontiers in Genetics and Cytogenetic and Genome Research.

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