Béatrice Dott

1.5k total citations
28 papers, 964 citations indexed

About

Béatrice Dott is a scholar working on Pediatrics, Perinatology and Child Health, Surgery and Genetics. According to data from OpenAlex, Béatrice Dott has authored 28 papers receiving a total of 964 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Pediatrics, Perinatology and Child Health, 14 papers in Surgery and 9 papers in Genetics. Recurrent topics in Béatrice Dott's work include Prenatal Screening and Diagnostics (13 papers), Congenital Anomalies and Fetal Surgery (9 papers) and Urological Disorders and Treatments (5 papers). Béatrice Dott is often cited by papers focused on Prenatal Screening and Diagnostics (13 papers), Congenital Anomalies and Fetal Surgery (9 papers) and Urological Disorders and Treatments (5 papers). Béatrice Dott collaborates with scholars based in France and Switzerland. Béatrice Dott's co-authors include Claude Stoll, Yves Alembik, Marie‐Paule Roth, Josué Feingold, Lewis B. Holmes, James F. Reynolds, Bérénice Doray, I. Nisand, M. Köhler and Bernard Gasser and has published in prestigious journals such as American Journal of Obstetrics and Gynecology, American Journal of Medical Genetics and Clinical Genetics.

In The Last Decade

Béatrice Dott

27 papers receiving 932 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Béatrice Dott France 18 418 311 279 207 160 28 964
Josef Wisser Switzerland 17 265 0.6× 168 0.5× 554 2.0× 85 0.4× 109 0.7× 49 897
Paulo Ricardo Gazzola Zen Brazil 16 233 0.6× 391 1.3× 230 0.8× 371 1.8× 115 0.7× 147 1.0k
B Dott France 22 847 2.0× 348 1.1× 469 1.7× 292 1.4× 207 1.3× 58 1.6k
María Luisa Martínez‐Frías Spain 22 638 1.5× 577 1.9× 453 1.6× 445 2.1× 153 1.0× 51 1.7k
Sebastiano Bianca Italy 14 253 0.6× 97 0.3× 237 0.8× 213 1.0× 79 0.5× 57 729
Mario Messina Italy 17 522 1.2× 129 0.4× 122 0.4× 166 0.8× 154 1.0× 111 1.0k
Marie‐Noel Westgate United States 12 214 0.5× 97 0.3× 245 0.9× 99 0.5× 66 0.4× 21 551
Yaron Zalel Israel 24 350 0.8× 206 0.7× 577 2.1× 103 0.5× 126 0.8× 62 1.4k
Ingrid Witters Belgium 19 476 1.1× 203 0.7× 681 2.4× 117 0.6× 187 1.2× 68 1.4k
Giorgio Adriano Paskulin Brazil 17 195 0.5× 344 1.1× 190 0.7× 351 1.7× 98 0.6× 89 899

Countries citing papers authored by Béatrice Dott

Since Specialization
Citations

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

Fields of papers citing papers by Béatrice Dott

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Béatrice Dott

This figure shows the co-authorship network connecting the top 25 collaborators of Béatrice Dott. A scholar is included among the top collaborators of Béatrice Dott 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 Béatrice Dott. Béatrice Dott 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
1.
Stoll, Claude, Béatrice Dott, Yves Alembik, & Marie‐Paule Roth. (2025). Co-occurring non-urinary congenital anomalies among cases with congenital anomalies of the kidney and urinary tract. European Journal of Medical Genetics. 74. 105000–105000.
2.
Stoll, Claude, Béatrice Dott, Yves Alembik, & Marie‐Paule Roth. (2023). Associated anomalies in anophthalmia and microphthalmia. European Journal of Medical Genetics. 67. 104892–104892. 1 indexed citations
3.
Stoll, Claude, et al.. (2020). Associated anomalies in cases with congenital clubfoot. American Journal of Medical Genetics Part A. 182(9). 2027–2036. 7 indexed citations
4.
Stoll, Claude, Béatrice Dott, & Marie‐Paule Roth. (2019). Associated anomalies in cases with agenesis of the corpus callosum. American Journal of Medical Genetics Part A. 179(10). 2101–2111. 17 indexed citations
5.
Stoll, Claude, Yves Alembik, Béatrice Dott, & Marie‐Paule Roth. (2016). Associated anomalies in cases with anotia and microtia. European Journal of Medical Genetics. 59(12). 607–614. 19 indexed citations
6.
Stoll, Claude, Béatrice Dott, Yves Alembik, & Marie‐Paule Roth. (2015). Associated congenital anomalies among cases with Down syndrome. European Journal of Medical Genetics. 58(12). 674–680. 149 indexed citations
7.
Stoll, Claude, Béatrice Dott, Yves Alembik, & Marie‐Paule Roth. (2014). Associated noncardiac congenital anomalies among cases with congenital heart defects. European Journal of Medical Genetics. 58(2). 75–85. 33 indexed citations
8.
Stoll, Claude, Béatrice Dott, Yves Alembik, & Marie‐Paule Roth. (2014). Associated nonurinary congenital anomalies among infants with congenital anomalies of kidney and urinary tract (CAKUT). European Journal of Medical Genetics. 57(7). 322–328. 48 indexed citations
9.
Schaefer, Élise, B. Monga, Béatrice Dott, et al.. (2014). Neural Tube Defects: The Experience of the Registry of Congenital Malformations of Alsace, France, 1995-2009. Fetal Diagnosis and Therapy. 37(1). 6–17. 12 indexed citations
10.
Stoll, Claude, Béatrice Dott, Yves Alembik, & Marie‐Paule Roth. (2012). Associated malformations among infants with anophthalmia and microphthalmia. Birth Defects Research Part A Clinical and Molecular Teratology. 94(3). 147–152. 14 indexed citations
11.
Stoll, Claude, Béatrice Dott, Yves Alembik, & Marie‐Paule Roth. (2011). Associated malformations among infants with neural tube defects. American Journal of Medical Genetics Part A. 155(3). 565–568. 36 indexed citations
12.
Stoll, Claude, Yves Alembik, Béatrice Dott, & Marie‐Paule Roth. (2010). Associated malformations in patients with limb reduction deficiencies. European Journal of Medical Genetics. 53(5). 286–290. 35 indexed citations
13.
Stoll, Claude, Yves Alembik, Béatrice Dott, & Marie‐Paule Roth. (2008). Omphalocele and gastroschisis and associated malformations. American Journal of Medical Genetics Part A. 146A(10). 1280–1285. 89 indexed citations
14.
Stoll, Claude, Yves Alembik, Béatrice Dott, & Marie‐Paule Roth. (2007). Associated malformations in patients with oral clefts. American Journal of Medical Genetics Part A. 143A(20). 2463–2465. 19 indexed citations
15.
Stoll, Claude, Béatrice Dott, Yves Alembik, & Marie‐Paule Roth. (2000). Evaluation of prenatal diagnosis of cleft lip/palate by foetal ultrasonographic examination. Annales de Génétique. 43(1). 11–14. 46 indexed citations
16.
Stoll, Claude, Marie‐Paule Roth, Béatrice Dott, & Yves Alembik. (1999). Study of 290 Cases of Polyhydramnios and Congenital Malformations in a Series of 225,669 Consecutive Births. Public Health Genomics. 2(1). 36–42. 17 indexed citations
17.
Stoll, Claude, Yves Alembik, Béatrice Dott, & Josué Feingold. (1994). Parental consanguinity as a cause of increased incidence of birth defects in a study of 131, 760 consecutive birthsxs. American Journal of Medical Genetics. 49(1). 114–117. 34 indexed citations
18.
Stoll, Claude, Yves Alembik, & Béatrice Dott. (1991). Study of 156 cases of polyhydramnios and congenital malformations in a series of 118,265 consecutive births. American Journal of Obstetrics and Gynecology. 165(3). 586–590. 29 indexed citations
19.
Stoll, Claude, Béatrice Dott, Marie‐Paule Roth, & Yves Alembik. (1989). Birth prevalence rates of skeletal dysplasias. Clinical Genetics. 35(2). 88–92. 176 indexed citations
20.
Stoll, Claude, et al.. (1985). Male‐to‐male transmission of the hypertelorism‐hypospadias (BBB) syndrome. American Journal of Medical Genetics. 20(2). 221–225. 13 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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