Emiel Baten

405 total citations
8 papers, 234 citations indexed

About

Emiel Baten is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Emiel Baten has authored 8 papers receiving a total of 234 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Genetics and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Emiel Baten's work include Congenital limb and hand anomalies (2 papers), Hearing, Cochlea, Tinnitus, Genetics (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Emiel Baten is often cited by papers focused on Congenital limb and hand anomalies (2 papers), Hearing, Cochlea, Tinnitus, Genetics (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Emiel Baten collaborates with scholars based in Belgium, United States and Netherlands. Emiel Baten's co-authors include Koenraad Devriendt, Joris Vermeesch, Thomy de Ravel, JP Fryns, Gabriele Krüger, Olaf Hiort, Katarina Dathe, Bianca P. Hennig, Petra Seemann and Johannes Weigel and has published in prestigious journals such as The American Journal of Human Genetics, Journal of Medical Genetics and Pediatric Nephrology.

In The Last Decade

Emiel Baten

8 papers receiving 216 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Emiel Baten Belgium	8	147	133	32	31	30	8	234
M. Elizabeth McCready Canada	10	120 0.8×	80 0.6×	39 1.2×	17 0.5×	14 0.5×	25	254
Jill K. Northup United States	8	155 1.1×	115 0.9×	26 0.8×	10 0.3×	39 1.3×	13	224
Heide Seidel Germany	14	192 1.3×	182 1.4×	32 1.0×	18 0.6×	33 1.1×	24	337
J.G. Dauwerse Netherlands	6	129 0.9×	211 1.6×	17 0.5×	19 0.6×	52 1.7×	7	307
Jennifer McDaid United Kingdom	8	99 0.7×	271 2.0×	21 0.7×	21 0.7×	24 0.8×	8	325
Patrick L. Wilmot United States	10	148 1.0×	95 0.7×	49 1.5×	22 0.7×	29 1.0×	26	238
M E Oude Luttikhuis United Kingdom	8	256 1.7×	221 1.7×	22 0.7×	38 1.2×	18 0.6×	9	355
Aline Receveur France	9	109 0.7×	81 0.6×	50 1.6×	11 0.4×	29 1.0×	22	200
Carmelo Laganà Italy	9	148 1.0×	137 1.0×	62 1.9×	12 0.4×	33 1.1×	21	266
Jeannette Hoogeboom Netherlands	9	201 1.4×	155 1.2×	34 1.1×	22 0.7×	8 0.3×	13	325

Countries citing papers authored by Emiel Baten

Since Specialization

Citations

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

Fields of papers citing papers by Emiel Baten

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emiel Baten

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

All Works

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8 of 8 papers shown

1.

Klopocki, Eva, Bianca P. Hennig, Katarina Dathe, et al.. (2010). Deletion and Point Mutations of PTHLH Cause Brachydactyly Type E. The American Journal of Human Genetics. 86(3). 434–439. 93 indexed citations

2.

Dimitrov, Boyan, Irina Balikova, Thomy de Ravel, et al.. (2010). 2q31.1 microdeletion syndrome: redefining the associated clinical phenotype. Journal of Medical Genetics. 48(2). 98–104. 38 indexed citations

3.

Declau, Frank, et al.. (2005). Stapes Ankylosis in a Family with a Novel NOG Mutation: Otologic Features of the Facioaudiosymphalangism Syndrome. Otology & Neurotology. 26(5). 934–940. 12 indexed citations

4.

Declau, Frank, et al.. (2005). The facio-audio-symphalangism syndrome in a four generation family with a nonsense mutation in the NOG-gene. Clinical Dysmorphology. 14(2). 73–80. 17 indexed citations

5.

Vermeesch, Joris, Emiel Baten, JP Fryns, & Koenraad Devriendt. (2002). Ring syndrome caused by ring chromosome 7 without loss of subtelomeric sequences. Clinical Genetics. 62(5). 415–417. 32 indexed citations

6.

Fryns, Jean‐Pierre, Eric Legius, Koenraad Devriendt, et al.. (1996). Cohen syndrome: the clinical symptoms and stigmata at a young age. Clinical Genetics. 49(5). 237–241. 26 indexed citations

7.

Proesmans, Willem, Emiel Baten, & Boudewijn Van Damme. (1995). A boy with acute renal failure. Pediatric Nephrology. 9(3). 389–391. 7 indexed citations

8.

Legius, Eric, Emiel Baten, Michel Stul, Peter Marynen, & Jean-Jacques Cassiman. (1990). Sporadic late onset ornithine transcarbamylase deficiency in a boy with somatic mosaicism for an intragenic deletion. Clinical Genetics. 38(2). 155–159. 9 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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