K Devriendt

618 total citations
6 papers, 475 citations indexed

About

K Devriendt is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, K Devriendt has authored 6 papers receiving a total of 475 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 2 papers in Molecular Biology and 2 papers in Pulmonary and Respiratory Medicine. Recurrent topics in K Devriendt's work include Genomic variations and chromosomal abnormalities (3 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Congenital Heart Disease Studies (1 paper). K Devriendt is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Congenital Heart Disease Studies (1 paper). K Devriendt collaborates with scholars based in United States, Belgium and Japan. K Devriendt's co-authors include Marc Gewillig, M Dumoulin, J P Fryns, Ann Swillen, Bénédicte Eyskens, Eric Legius, Noritaka Iwatani, Teruhisa Miike, Hiroyo Mabe and Peter Groenen and has published in prestigious journals such as The Journal of Pediatrics, Genomics and Journal of Medical Genetics.

In The Last Decade

K Devriendt

6 papers receiving 460 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
K Devriendt United States	6	384	185	181	151	55	6	475
Luís Fernández Spain	12	261 0.7×	306 1.7×	92 0.5×	77 0.5×	25 0.5×	23	565
Margaret N. Berry United States	9	182 0.5×	109 0.6×	64 0.4×	61 0.4×	14 0.3×	15	275
Federica Consoli Italy	11	357 0.9×	143 0.8×	85 0.5×	163 1.1×	15 0.3×	21	497
W Schönberger Germany	11	223 0.6×	154 0.8×	77 0.4×	25 0.2×	8 0.1×	31	440
Nils Peeters Belgium	10	112 0.3×	145 0.8×	115 0.6×	11 0.1×	27 0.5×	16	310
Tiziana Filippi Italy	9	207 0.5×	374 2.0×	13 0.1×	25 0.2×	67 1.2×	10	539
Y. Fukushima Japan	8	249 0.6×	197 1.1×	22 0.1×	20 0.1×	35 0.6×	15	349
Christalena Sofocleous Greece	14	218 0.6×	261 1.4×	11 0.1×	17 0.1×	67 1.2×	45	459
Ganka Douglas United States	10	228 0.6×	161 0.9×	17 0.1×	12 0.1×	36 0.7×	13	336
Sandra Whalen France	13	268 0.7×	157 0.8×	24 0.1×	19 0.1×	18 0.3×	28	417

Countries citing papers authored by K Devriendt

Since Specialization

Citations

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

Fields of papers citing papers by K Devriendt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of K Devriendt

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

All Works

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6 of 6 papers shown

1.

Mols, Raf, et al.. (2002). Involvement of a palindromic chromosome 22‐specific low‐copy repeat in a constitutional t(X; 22)(q27;q11). Clinical Genetics. 62(5). 410–414. 16 indexed citations

2.

Iwatani, Noritaka, et al.. (2000). Deletion of NKX2.1 gene encoding thyroid transcription factor-1 in two siblings with hypothyroidism and respiratory failure. The Journal of Pediatrics. 137(2). 272–276. 122 indexed citations

3.

Groenen, Peter, et al.. (1998). Rearrangement of the HumanCDC5LGene by a t(6;19)(p21;q13.1) in a Patient with Multicystic Renal Dysplasia. Genomics. 49(2). 218–229. 31 indexed citations

4.

Petit, P., et al.. (1998). Unusual de novo t(13;15)(q12.1;p13) translocation leading to complex mosaicism including jumping translocation.. PubMed. 41(1). 22–6. 10 indexed citations

5.

Petit, P., K Devriendt, M Azou, Marc Gewillig, & Jean‐Pierre Fryns. (1998). Terminal deletion of chromosome 10q26: delineation of two clinical phenotypes.. PubMed. 9(4). 271–5. 13 indexed citations

6.

Swillen, Ann, K Devriendt, Eric Legius, et al.. (1997). Intelligence and psychosocial adjustment in velocardiofacial syndrome: a study of 37 children and adolescents with VCFS.. Journal of Medical Genetics. 34(6). 453–458. 283 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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