Anne Bazin

1.3k total citations
16 papers, 195 citations indexed

About

Anne Bazin is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Anne Bazin has authored 16 papers receiving a total of 195 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Pediatrics, Perinatology and Child Health, 11 papers in Genetics and 4 papers in Molecular Biology. Recurrent topics in Anne Bazin's work include Prenatal Screening and Diagnostics (11 papers), Genomic variations and chromosomal abnormalities (7 papers) and Assisted Reproductive Technology and Twin Pregnancy (4 papers). Anne Bazin is often cited by papers focused on Prenatal Screening and Diagnostics (11 papers), Genomic variations and chromosomal abnormalities (7 papers) and Assisted Reproductive Technology and Twin Pregnancy (4 papers). Anne Bazin collaborates with scholars based in France, United Kingdom and Tunisia. Anne Bazin's co-authors include Sophie Julia, Claude Cancès, Julie Plaisancié, Adeline Vigouroux, Pascale Kleinfinger, F. Daffos, François Forestier, Bernard Guyot, Detlef Trost and Sonia Bouquillon and has published in prestigious journals such as SHILAP Revista de lepidopterología, The American Journal of Human Genetics and Fertility and Sterility.

In The Last Decade

Anne Bazin

16 papers receiving 169 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Anne Bazin France	8	119	90	74	42	12	16	195
Olga Žilina Estonia	12	242 2.0×	92 1.0×	132 1.8×	54 1.3×	11 0.9×	23	314
C. Le Caignec France	7	181 1.5×	136 1.5×	89 1.2×	32 0.8×	28 2.3×	7	242
Hélène Moirot France	9	119 1.0×	59 0.7×	76 1.0×	45 1.1×	20 1.7×	13	198
Prochi F. Madon India	7	190 1.6×	163 1.8×	102 1.4×	52 1.2×	20 1.7×	25	320
Fernando Santos Spain	9	228 1.9×	84 0.9×	193 2.6×	21 0.5×	23 1.9×	13	325
Imma Rost Germany	9	212 1.8×	45 0.5×	157 2.1×	74 1.8×	15 1.3×	24	322
Mylène Valduga France	8	169 1.4×	90 1.0×	76 1.0×	18 0.4×	19 1.6×	17	213
V.K. Maloney United Kingdom	9	263 2.2×	46 0.5×	174 2.4×	54 1.3×	10 0.8×	12	304
Geneviève Lefort France	13	262 2.2×	160 1.8×	148 2.0×	105 2.5×	15 1.3×	29	375

Countries citing papers authored by Anne Bazin

Since Specialization

Citations

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

Fields of papers citing papers by Anne Bazin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anne Bazin

This figure shows the co-authorship network connecting the top 25 collaborators of Anne Bazin. A scholar is included among the top collaborators of Anne Bazin 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 Anne Bazin. Anne Bazin is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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16 of 16 papers shown

Bazin, Anne, et al.. (2021). Pai syndrome: From the womb until 19 months of age, a neurological development success story. SHILAP Revista de lepidopterología. 9(7). e04499–e04499. 2 indexed citations

Gavard, Laurent, Anne Bazin, Fabien Guimiot, et al.. (2021). Case report: Antenatal diagnostic of a polymalformative syndrome due to biallelic BRCA2 mutations. SHILAP Revista de lepidopterología. 9(9). e04838–e04838. 2 indexed citations

Receveur, Aline, Sophie Brisset, Jelena Martinović, et al.. (2017). Prenatal diagnosis of isochromosome 20q in a fetus with vertebral anomaly and rocker-bottom feet. Taiwanese Journal of Obstetrics and Gynecology. 56(5). 677–680. 3 indexed citations

Vinatier, Isabelle, et al.. (2014). A late onset sickle cell disease reveals a mosaic segmental uniparental isodisomy of chromosome 11p15. Blood Cells Molecules and Diseases. 54(1). 53–55. 3 indexed citations

Plaisancié, Julie, Pascale Kleinfinger, Claude Cancès, et al.. (2014). Constitutional chromoanasynthesis: description of a rare chromosomal event in a patient. European Journal of Medical Genetics. 57(10). 567–570. 28 indexed citations

Quēlin, Chloé, Emmanuel Spaggiari, Suonavy Khung‐Savatovsky, et al.. (2014). Inversion duplication deletions involving the long arm of chromosome 13: Phenotypic description of additional three fetuses and genotype–phenotype correlation. American Journal of Medical Genetics Part A. 164(10). 2504–2509. 10 indexed citations

Guimiot, Fabien, Céline Dupont, Azzedine Aboura, et al.. (2012). Maternal transmission of interstitial 8p23.1 deletion detected during prenatal diagnosis. American Journal of Medical Genetics Part A. 161(1). 208–213. 21 indexed citations

Meyer, Esther, Christopher J. Ricketts, Neil V. Morgan, et al.. (2010). Mutations in FLVCR2 Are Associated with Proliferative Vasculopathy and Hydranencephaly-Hydrocephaly Syndrome (Fowler Syndrome). The American Journal of Human Genetics. 86(3). 471–478. 46 indexed citations

Anselem, Olivia, Anne Bazin, Charlotte Mechler, et al.. (2010). Prenatal Diagnosis of 18q-Syndrome: A Case of Fetal Mosaicism with a Normal Karyotype in Chorionic Villi. Fetal Diagnosis and Therapy. 28(3). 180–185. 1 indexed citations

10.

Petit, Florence, Muriel Holder‐Espinasse, Bénédicte Duban‐Bedu, et al.. (2010). Trisomy 7 mosaicism prenatally misdiagnosed and maternal uniparental disomy in a child with pigmentary mosaicism and Russell– Silver syndrome. Clinical Genetics. 81(3). 265–271. 28 indexed citations

11.

Williams, Denise, Chirag Patel, Pierre Déchelotte, et al.. (2009). Fowler syndrome—A clinical, radiological, and pathological study of 14 cases. American Journal of Medical Genetics Part A. 152A(1). 153–160. 11 indexed citations

12.

Simon‐Bouy, Brigitte, M Plachot, Ali H. Mokdad, et al.. (2004). Diagnostic prénatal d’une probable chimère humaine après fécondation in vitro. Gynécologie Obstétrique & Fertilité. 32(2). 143–146. 1 indexed citations

13.

Simon‐Bouy, Brigitte, M Plachot, Ali H. Mokdad, et al.. (2003). Possible human chimera detected prenatally after in vitro fertilization: a case report. Prenatal Diagnosis. 23(11). 935–937. 10 indexed citations

14.

Plachot, M, et al.. (2002). Possible human chimera detected prenatally after in vitro fertilization: A case report. Fertility and Sterility. 78. S146–S146. 2 indexed citations

15.

Gérard‐Blanluet, Marion, et al.. (2001). Mosaic trisomy 15 and hemihypertrophy. Annales de Génétique. 44(3). 143–148. 5 indexed citations

16.

Guyot, Bernard, et al.. (1988). Prenatal diagnosis with biotinylated chromosome specific probes. Prenatal Diagnosis. 8(7). 485–493. 22 indexed citations

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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