Patrick Kools

1.9k total citations · 1 hit paper
24 papers, 1.5k citations indexed

About

Patrick Kools is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Pathology and Forensic Medicine. According to data from OpenAlex, Patrick Kools has authored 24 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 9 papers in Pulmonary and Respiratory Medicine and 4 papers in Pathology and Forensic Medicine. Recurrent topics in Patrick Kools's work include Sarcoma Diagnosis and Treatment (8 papers), Wnt/β-catenin signaling in development and cancer (8 papers) and Cancer-related gene regulation (4 papers). Patrick Kools is often cited by papers focused on Sarcoma Diagnosis and Treatment (8 papers), Wnt/β-catenin signaling in development and cancer (8 papers) and Cancer-related gene regulation (4 papers). Patrick Kools collaborates with scholars based in Belgium, Germany and United States. Patrick Kools's co-authors include Frans van Roy, Friedel Nollet, Herman Van den Berghe, Paola Dal Cin, Wim J.M. Van de Ven, Eric Schoenmakers, Wim Van de Ven, Jolanda van Hengel, Stefan Bonné and Christoph Redies and has published in prestigious journals such as Journal of Molecular Biology, Oncogene and Biochemical Journal.

In The Last Decade

Patrick Kools

24 papers receiving 1.5k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Phylogenetic analysis of the cadherin superfamily allows identification of six major subfamilies besides several solitary members 1 1Edited by M. Yaniv

2000 573 citations Friedel Nollet, Patrick Kools et al. Journal of Molecular Biology profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Patrick Kools Belgium	17	975	299	286	173	168	24	1.5k
Chester J. Herman United States	18	496 0.5×	248 0.8×	152 0.5×	158 0.9×	334 2.0×	35	1.5k
Amanda Mikels United States	11	2.0k 2.1×	196 0.7×	259 0.9×	196 1.1×	62 0.4×	13	2.4k
Lisa D. Urness United States	17	1.6k 1.7×	330 1.1×	308 1.1×	584 3.4×	51 0.3×	22	2.4k
Heinrich Schrewe Germany	28	1.5k 1.6×	93 0.3×	182 0.6×	124 0.7×	62 0.4×	46	2.2k
Nina Schumacher Germany	15	866 0.9×	80 0.3×	165 0.6×	91 0.5×	73 0.4×	24	1.2k
Sahar Nissim United States	15	1.4k 1.5×	302 1.0×	217 0.8×	130 0.8×	70 0.4×	20	2.1k
Mark C. Hanks United States	15	1.9k 2.0×	103 0.3×	189 0.7×	205 1.2×	44 0.3×	18	2.5k
Elena Torban Canada	23	1.4k 1.5×	167 0.6×	319 1.1×	83 0.5×	66 0.4×	43	1.8k
Cantas Alev Japan	21	1.1k 1.1×	105 0.4×	152 0.5×	161 0.9×	30 0.2×	47	1.5k
Paula Lewis United States	13	2.7k 2.8×	294 1.0×	435 1.5×	163 0.9×	121 0.7×	17	3.4k

Countries citing papers authored by Patrick Kools

Since Specialization

Citations

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

Fields of papers citing papers by Patrick Kools

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Patrick Kools

This figure shows the co-authorship network connecting the top 25 collaborators of Patrick Kools. A scholar is included among the top collaborators of Patrick Kools 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 Patrick Kools. Patrick Kools 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

Kools, Patrick, et al.. (2017). Cyber Security in Oil & Gas: Outsourced or In-House?. 2 indexed citations

Kools, Patrick, et al.. (2005). δ-Protocadherins: a gene family expressed differentially in the mouse brain. Cellular and Molecular Life Sciences. 62(11). 1247–1259. 104 indexed citations

Janssens, Barbara, Bhagyalaxmi Mohapatra, Matteo Vatta, et al.. (2003). Assessment of the CTNNA3 gene encoding human αT-catenin regarding its involvement in dilated cardiomyopathy. Human Genetics. 112(3). 227–236. 39 indexed citations

Kools, Patrick, et al.. (2001). The human and murine protocadherin‐β one‐exon gene families show high evolutionary conservation, despite the difference in gene number. FEBS Letters. 495(1-2). 120–125. 23 indexed citations

Kools, Patrick, Griet Van Imschoot, & Frans van Roy. (2000). Characterization of Three Novel Human Cadherin Genes (CDH7, CDH19, and CDH20) Clustered on Chromosome 18q22–q23 and with High Homology to Chicken Cadherin-7. Genomics. 68(3). 283–295. 24 indexed citations

Nollet, Friedel, Patrick Kools, & Frans van Roy. (2000). Phylogenetic analysis of the cadherin superfamily allows identification of six major subfamilies besides several solitary members 1 1Edited by M. Yaniv. Journal of Molecular Biology. 299(3). 551–572. 573 indexed citations breakdown →

Kools, Patrick, et al.. (1999). Assignment<footref rid="foot01"><sup>1</sup></footref> of cadherin-4 (R-cadherin, CDH4) to human chromosome band 20q13.3. Cytogenetic and Genome Research. 86(1). 26–27. 6 indexed citations

Kools, Patrick, et al.. (1999). The human cadherin‐10 gene: complete coding sequence, predominant expression in the brain, and mapping on chromosome 5p13–14. FEBS Letters. 452(3). 328–334. 15 indexed citations

Berner, Jeanne-Marie, Leonardo A. Meza‐Zepeda, Patrick Kools, et al.. (1997). HMGIC, the gene for an architectural transcription factor, is amplified and rearranged in a subset of human sarcomas. Oncogene. 14(24). 2935–2941. 79 indexed citations

10.

Wanschura, Sylke, Gazanfer Belge, Göran Stenman, et al.. (1996). Mapping of the translocation breakpoints of primary pleomorphic adenomas and lipomas within a common region of chromosome 12. Cancer Genetics and Cytogenetics. 86(1). 39–45. 15 indexed citations

11.

Kools, Patrick & Wim J.M. Van de Ven. (1996). Amplification of a rearranged form of the high-mobility group protein gene HMGIC in OsA-CI osteosarcoma cells. Cancer Genetics and Cytogenetics. 91(1). 1–7. 22 indexed citations

12.

Kools, Patrick, Sylke Wanschura, Eric Schoenmakers, et al.. (1995). Identification of the chromosome 12 translocation breakpoint region of a pleomorphic salivary gland adenoma with t(1;12)(p22;q15) as the sole cytogenetic abnormality. Cancer Genetics and Cytogenetics. 79(1). 1–7. 13 indexed citations

13.

Schoenmakers, Eric, Sylke Wanschura, Bernd Kazmierczak, et al.. (1995). Molecular characterization of mar, a multiple aberration region on human chromosome segment 12q13‐q15 implicated in various solid tumors. Genes Chromosomes and Cancer. 12(4). 296–303. 40 indexed citations

14.

Schoenmakers, Eric, Raf Mols, Sylke Wanschura, et al.. (1994). Identification, molecular cloning, and characterization of the chromosome 12 breakpoint cluster region of uterine leiomyomas. Genes Chromosomes and Cancer. 11(2). 106–118. 33 indexed citations

15.

Kools, Patrick, Anton Roebroek, Helgi J. K. van de Velde, et al.. (1994). Regional mapping of the human NSP gene to chromosome region 14q21→q22 by fluorescence in situ hybridization analysis. Cytogenetic and Genome Research. 66(1). 48–50. 16 indexed citations

16.

Forus, Anne, et al.. (1994). A long range restriction map spanning the myxoid liposarcoma breakpoint in the q13-14 region of human chromosome 12. Human Genetics. 94(3). 259–264. 5 indexed citations

17.

Schoenmakers, Eric, Patrick Kools, Raf Mols, et al.. (1994). Physical Mapping of Chromosome 12q Breakpoints in Lipoma, Pleomorphic Salivary Gland Adenoma, Uterine Leiomyoma, and Myxoid Liposarcoma. Genomics. 20(2). 210–222. 54 indexed citations

18.

Cin, Paola Dal, Patrick Kools, Raf Sciot, et al.. (1993). Cytogenetic and fluorescence in situ hybridization investigation of ring chromosomes characterizing a specific pathologic subgroup of adipose tissue tumors. Cancer Genetics and Cytogenetics. 68(2). 85–90. 146 indexed citations

19.

Kools, Patrick, Bernd Kazmierczak, Jörn Bullerdiek, et al.. (1993). Isolation of a somatic cell hybrid retaining the der(16)t(12;16)(q13;p11.2) from a myxoid liposarcoma cell line. Cytogenetic and Genome Research. 62(2-3). 159–161. 16 indexed citations

20.

Cin, Paola Dal, et al.. (1993). Rearrangement of 12q14‐15 in pulmonary chondroid hamartoma. Genes Chromosomes and Cancer. 8(2). 131–133. 38 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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