Julia Tantau

978 total citations
14 papers, 143 citations indexed

About

Julia Tantau is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Julia Tantau has authored 14 papers receiving a total of 143 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Pediatrics, Perinatology and Child Health, 9 papers in Genetics and 5 papers in Molecular Biology. Recurrent topics in Julia Tantau's work include Prenatal Screening and Diagnostics (8 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genetic Syndromes and Imprinting (2 papers). Julia Tantau is often cited by papers focused on Prenatal Screening and Diagnostics (8 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genetic Syndromes and Imprinting (2 papers). Julia Tantau collaborates with scholars based in France, Netherlands and Japan. Julia Tantau's co-authors include Géraldine Viot, G. Grangé, Jelena Martinović, D. Cabrol, Michel Vekemans, E. Pannier, Nicolas Chassaing, Trijnie Dijkhuizen, Josseline Kaplan and Férechté Encha‐Razavi and has published in prestigious journals such as American Journal of Obstetrics and Gynecology, Ultrasound in Obstetrics and Gynecology and Prenatal Diagnosis.

In The Last Decade

Julia Tantau

14 papers receiving 140 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Julia Tantau France	8	68	62	50	34	28	14	143
Françoise Ménez France	5	130 1.9×	53 0.9×	37 0.7×	26 0.8×	50 1.8×	5	218
Ellika Sahlin Sweden	9	82 1.2×	78 1.3×	72 1.4×	26 0.8×	10 0.4×	13	193
Stéphane Serero France	8	110 1.6×	188 3.0×	133 2.7×	43 1.3×	59 2.1×	15	328
Manisha Goyal India	8	36 0.5×	46 0.7×	48 1.0×	16 0.5×	7 0.3×	43	147
Dana Knutzen United States	7	63 0.9×	39 0.6×	48 1.0×	32 0.9×	15 0.5×	9	174
Eva Pompilii Italy	7	245 3.6×	145 2.3×	50 1.0×	34 1.0×	32 1.1×	13	298
Y. Hillion France	10	175 2.6×	50 0.8×	36 0.7×	65 1.9×	18 0.6×	14	239
Daniel Doherty United States	5	53 0.8×	56 0.9×	49 1.0×	12 0.4×	9 0.3×	9	113
Thomas Nüßlein Germany	3	26 0.4×	137 2.2×	73 1.5×	20 0.6×	12 0.4×	6	225
Sofìa Kitsiou Greece	10	73 1.1×	155 2.5×	71 1.4×	33 1.0×	28 1.0×	25	260

Countries citing papers authored by Julia Tantau

Since Specialization

Citations

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

Fields of papers citing papers by Julia Tantau

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Julia Tantau

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

All Works

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14 of 14 papers shown

Lœuillet, Laurence, Jean–Paul Duong Van Huyen, Bettina Bessières, et al.. (2020). Severe and progressive neuronal loss in myelomeningocele begins before 16 weeks of pregnancy. American Journal of Obstetrics and Gynecology. 223(2). 256.e1–256.e9. 20 indexed citations

Bèaufrere, Aurélie, Maryse Bonnière, Julia Tantau, et al.. (2018). Corpus Callosum Abnormalities and Short Femurs in Beckwith–Wiedemann Syndrome: A Report of Two Fetal Cases. Fetal and Pediatric Pathology. 37(6). 411–417. 3 indexed citations

Ravenswaaij‐Arts, Conny M.A. van, Julia Tantau, Nicole Corsten‐Janssen, et al.. (2013). Otocephaly-Dysgnathia Complex: Description of Four Cases and Confirmation of the Role of <b><i>OTX2</i></b>. Molecular Syndromology. 4(6). 302–305. 27 indexed citations

Essaoui, M., Mathilde Nizon, Julia Tantau, et al.. (2013). Monozygotic twins discordant for 18q21.2qter deletion detected by array CGH in amniotic fluid. European Journal of Medical Genetics. 56(9). 502–505. 12 indexed citations

Cuisset, Laurence, Vassilis Tsatsaris, Julia Tantau, et al.. (2012). First reported case of interstitial 15 q15.3‐q21.3 deletion diagnosed prenatally and characterized with array CGH in a fetus with an isolated short femur. American Journal of Medical Genetics Part A. 158A(3). 617–621. 1 indexed citations

Khung‐Savatovsky, Suonavy, Géraldine Viot, Julia Tantau, et al.. (2011). Fetopathologic examination for early termination of pregnancy: dogma or necessity?. American Journal of Obstetrics and Gynecology. 205(5). 467.e1–467.e9. 3 indexed citations

Grangé, G., et al.. (2006). Fréquence des malformations associées à la trisomie 21: À propos de 101 cas fcetopathologiques. Journal de gynécologie, obstétrique et biologie de la reproduction. Supplément. 35(5). 477–482. 2 indexed citations

Grangé, G., et al.. (2006). Fréquence des malformations associées à la trisomie 21. Journal de gynécologie, obstétrique et biologie de la reproduction. Supplément. 35(5). 477–482. 4 indexed citations

Malan, Valérie, Jelena Martinović, Damien Sanlaville, et al.. (2006). Molecular characterisation of a prenatally diagnosed 5q15q21.3 deletion and review of the literature. Prenatal Diagnosis. 26(3). 231–238. 7 indexed citations

10.

Viot, Géraldine, Pascale Sonigo, Isabelle Simon, et al.. (2003). Neocortical neuronal arrangement in LIS1 and DCX lissencephaly may be different. American Journal of Medical Genetics Part A. 126A(2). 123–128. 23 indexed citations

11.

Pannier, E., Géraldine Viot, M. C. Aubry, et al.. (2002). Congenital erythropoietic porphyria (Günther's disease): two cases with very early prenatal manifestation and cystic hygroma. Prenatal Diagnosis. 23(1). 25–30. 19 indexed citations

12.

Tantau, Julia, et al.. (2002). [Ultrasonographic and pathological correlation in a fetal intracranial cyst: a case of "diencephalo-synapsis"].. PubMed. 31(6). 600–3. 4 indexed citations

13.

Grangé, G., et al.. (2001). Prenatal diagnosis of fetal tail and postabortum anatomical description. Ultrasound in Obstetrics and Gynecology. 18(5). 531–533. 8 indexed citations

14.

Fert‐Ferrer, Sandra, Julia Tantau, Anne Lise Delezoïde, et al.. (2000). Subtle familial unbalanced translocation t(8;11)(p23.2;p15.5) in two fetuses with Beckwith-Wiedemann features. Prenatal Diagnosis. 20(6). 511–515. 10 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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