Karin Segers

1.7k total citations
29 papers, 835 citations indexed

About

Karin Segers is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Karin Segers has authored 29 papers receiving a total of 835 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 16 papers in Molecular Biology and 7 papers in Pathology and Forensic Medicine. Recurrent topics in Karin Segers's work include BRCA gene mutations in cancer (7 papers), Genetic Syndromes and Imprinting (6 papers) and Genetic factors in colorectal cancer (6 papers). Karin Segers is often cited by papers focused on BRCA gene mutations in cancer (7 papers), Genetic Syndromes and Imprinting (6 papers) and Genetic factors in colorectal cancer (6 papers). Karin Segers collaborates with scholars based in Belgium, United States and France. Karin Segers's co-authors include Michel Georges, Carole Charlier, Noelle Cockett, T. L. Shay, Gàbor Gyapay, Latifa Karim, Vincent Bours, Stéphane Berghmans, Jean Weissenbach and Olivier Jaillon and has published in prestigious journals such as Nature Genetics, The Journal of Clinical Endocrinology & Metabolism and Scientific Reports.

In The Last Decade

Karin Segers

28 papers receiving 806 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Karin Segers Belgium	15	565	533	149	122	74	29	835
Bérengère de Martinville United States	17	616 1.1×	389 0.7×	83 0.6×	69 0.6×	56 0.8×	27	980
M. E. Robertson United Kingdom	9	457 0.8×	206 0.4×	68 0.5×	96 0.8×	37 0.5×	13	712
N. Alice Yamada United States	14	920 1.6×	652 1.2×	115 0.8×	267 2.2×	26 0.4×	18	1.3k
Martine Doco‐Fenzy France	15	349 0.6×	302 0.6×	80 0.5×	59 0.5×	35 0.5×	29	690
Andrew R. Cullinane United States	16	390 0.7×	401 0.8×	111 0.7×	12 0.1×	39 0.5×	20	824
Julien Thévenon France	15	450 0.8×	474 0.9×	54 0.4×	41 0.3×	27 0.4×	51	798
Cathy M. Tuck‐Müller United States	17	515 0.9×	428 0.8×	157 1.1×	49 0.4×	28 0.4×	37	855
Duen-Mei Wang China	12	280 0.5×	216 0.4×	26 0.2×	93 0.8×	34 0.5×	19	576
Christopher R. Futtner United States	12	695 1.2×	232 0.4×	75 0.5×	164 1.3×	14 0.2×	16	983
Kirsten R. McEwen United Kingdom	7	847 1.5×	356 0.7×	186 1.2×	97 0.8×	23 0.3×	8	973

Countries citing papers authored by Karin Segers

Since Specialization

Citations

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

Fields of papers citing papers by Karin Segers

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Karin Segers

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

All Works

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20 of 20 papers shown

Segers, Karin, Pascal Wolter, Joëlle Collignon, et al.. (2024). Digenic Inheritance of Mutations in Homologous Recombination Genes in Cancer Patients. Journal of Personalized Medicine. 14(6). 584–584.

Fasquelle, Corinne, Keith Durkin, Maria Artesi, et al.. (2024). Genetic evaluation of patients with multiple primary cancers. Oncology Letters. 29(1). 4–4. 1 indexed citations

Marcke, Cédric van, Karin Segers, Corinne Fasquelle, et al.. (2022). Case Report Series: Aggressive HR Deficient Colorectal Cancers Related to BRCA1 Pathogenic Germline Variants. Frontiers in Oncology. 12. 835581–835581. 4 indexed citations

Ramaekers, V., Karin Segers, J.M. Sequeira, et al.. (2018). Genetic assessment and folate receptor autoantibodies in infantile-onset cerebral folate deficiency (CFD) syndrome. Molecular Genetics and Metabolism. 124(1). 87–93. 18 indexed citations

Corman, Vinciane, Iulia Potorac, Karin Segers, et al.. (2016). Breast cancer in a male-to-female transsexual patient with a BRCA2 mutation. Endocrine Related Cancer. 23(5). 391–397. 25 indexed citations

Segers, Karin, et al.. (2015). [PHARMACOGENOMICS AND PERSONALIZED MEDICINE: TOWARDS A SYSTEMATIC GENOMIC SCREENING?].. PubMed. 70(5-6). 251–6. 1 indexed citations

Josse, Claire, et al.. (2015). BRCA1 germline mutation and glioblastoma development: report of cases. BMC Cancer. 15(1). 181–181. 19 indexed citations

Josse, Claire, Bouchra Boujemla, Pierre Frères, et al.. (2015). Evaluation of BRCA1-related molecular features and microRNAs as prognostic factors for triple negative breast cancers. BMC Cancer. 15(1). 755–755. 19 indexed citations

Boemer, François, Yves Cornet, Cécile Libioulle, et al.. (2011). 3-years experience review of neonatal screening for hemoglobin disorders using tandem mass spectrometry. Clinica Chimica Acta. 412(15-16). 1476–1479. 28 indexed citations

10.

Debray, François‐Guillaume, et al.. (2010). Free Sialic Acid Storage Disease Mimicking Cerebral Palsy and Revealed by Blood Smear Examination. The Journal of Pediatrics. 158(1). 165–165.e1. 5 indexed citations

11.

Mutesa, Léon, Geneviève Pierquin, Nicolas Janin, et al.. (2008). Germline PTPN11 missense mutation in a case of Noonan syndrome associated with mediastinal and retroperitoneal neuroblastic tumors. Cancer Genetics and Cytogenetics. 182(1). 40–42. 22 indexed citations

12.

Mutesa, Léon, Abul Kalam Azad, Catherine Verhaeghe, et al.. (2008). Genetic Analysis of Rwandan Patients With Cystic Fibrosis-Like Symptoms. CHEST Journal. 135(5). 1233–1242. 24 indexed citations

13.

Mutesa, Léon, et al.. (2008). Spinocerebellar Ataxia Type 2 (SCA2): Clinical Features and Genetic Analysis. Journal of Tropical Pediatrics. 54(5). 350–352. 12 indexed citations

14.

Cockett, Noelle, Maria A. Smit, Christopher A. Bidwell, et al.. (2004). The callipyge mutation and other genes that affect muscle hypertrophy in sheep. Genetics Selection Evolution. 37(S1). S65–S81. 45 indexed citations

15.

Georges, Michel, Francis F. Barillet, Nadine Buys, et al.. (2002). On the contribution of imprinted loci to variation in animal body composition.. 1–4. 1 indexed citations

16.

Charlier, Carole, Karin Segers, Danny Wagenaar, et al.. (2001). Human–Ovine Comparative Sequencing of a 250-kb Imprinted Domain Encompassing the Callipyge (clpg) Locus and Identification of Six Imprinted Transcripts: DLK1, DAT, GTL2, PEG11, antiPEG11, and MEG8. Genome Research. 11(5). 850–862. 169 indexed citations

17.

Paulsen, Martina, Shuji Takada, Neil A. Youngson, et al.. (2001). Comparative Sequence Analysis of the Imprinted Dlk1–Gtl2 Locus in Three Mammalian Species Reveals Highly Conserved Genomic Elements and Refines Comparison with the Igf2–H19 Region. Genome Research. 11(12). 2085–2094. 108 indexed citations

18.

Charlier, Carole, Karin Segers, Latifa Karim, et al.. (2001). The callipyge mutation enhances the expression of coregulated imprinted genes in cis without affecting their imprinting status. Nature Genetics. 27(4). 367–369. 137 indexed citations

19.

Shay, T. L., Stéphane Berghmans, Karin Segers, et al.. (2001). Fine-mapping and construction of a bovine contig spanning the ovine callipyge locus. Mammalian Genome. 12(2). 141–149. 20 indexed citations

20.

Segers, Karin, Stéphane Berghmans, Michel Georges, et al.. (2000). Construction and characterization of an ovine BAC contig spanning the callipyge locus. Animal Genetics. 31(6). 352–359. 15 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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