Hans Albertsen

8.2k total citations · 1 hit paper
42 papers, 3.3k citations indexed

About

Hans Albertsen is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Hans Albertsen has authored 42 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 15 papers in Genetics and 10 papers in Pathology and Forensic Medicine. Recurrent topics in Hans Albertsen's work include Genetic factors in colorectal cancer (10 papers), Genomic variations and chromosomal abnormalities (9 papers) and Epigenetics and DNA Methylation (8 papers). Hans Albertsen is often cited by papers focused on Genetic factors in colorectal cancer (10 papers), Genomic variations and chromosomal abnormalities (9 papers) and Epigenetics and DNA Methylation (8 papers). Hans Albertsen collaborates with scholars based in United States, Poland and United Kingdom. Hans Albertsen's co-authors include Wade S. Samowitz, Martha L. Slattery, Roger K. Wolff, Carol Sweeney, Jennifer S. Herrick, Theodore R. Levin, Maureen A. Murtaugh, Denis Le Paslier, Howard M. Cann and Hadi Abderrahim and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Nature Genetics.

In The Last Decade

Hans Albertsen

41 papers receiving 3.2k citations

Hit Papers

align trajectories sort by overperformance

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.

Poor Survival Associated with the BRAF V600E Mutation in Microsatellite-Stable Colon Cancers

2005 592 citations Wade S. Samowitz, Carol Sweeney et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Hans Albertsen United States	26	1.5k	1.2k	1.2k	563	518	42	3.3k
Michael Zimmer United States	24	1.6k 1.1×	711 0.6×	690 0.6×	463 0.8×	817 1.6×	52	3.1k
Robert Winqvist Finland	34	2.1k 1.4×	936 0.8×	479 0.4×	1.1k 1.9×	853 1.6×	89	3.3k
Harry Hou United States	18	3.8k 2.5×	530 0.4×	552 0.5×	1.4k 2.5×	453 0.9×	18	5.0k
Danny Liaw United States	9	4.5k 3.0×	1.2k 1.0×	884 0.7×	586 1.0×	989 1.9×	16	5.8k
Jacob Zhurinsky Israel	15	3.4k 2.3×	796 0.6×	289 0.2×	365 0.6×	341 0.7×	17	4.2k
Alain Eychène France	32	2.2k 1.4×	798 0.6×	270 0.2×	246 0.4×	333 0.6×	55	3.0k
Patricia Gorman United Kingdom	33	2.1k 1.4×	1.4k 1.2×	1.7k 1.4×	1.2k 2.1×	1.2k 2.3×	57	4.3k
Olga Aprelikova United States	30	2.8k 1.8×	1.0k 0.8×	163 0.1×	522 0.9×	1.1k 2.2×	48	3.7k
Shlomit Halachmi Israel	14	2.3k 1.5×	1.3k 1.0×	193 0.2×	1.2k 2.1×	408 0.8×	28	3.4k
Cor Breukel Netherlands	26	1.9k 1.3×	1.1k 0.9×	1.4k 1.2×	483 0.9×	537 1.0×	53	3.3k

Countries citing papers authored by Hans Albertsen

Since Specialization

Citations

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

Fields of papers citing papers by Hans Albertsen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hans Albertsen

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

Albertsen, Hans & Kenneth Ward. (2016). Genes Linked to Endometriosis by GWAS Are Integral to Cytoskeleton Regulation and Suggests That Mesothelial Barrier Homeostasis Is a Factor in the Pathogenesis of Endometriosis. Reproductive Sciences. 24(6). 803–811. 36 indexed citations

Chettier, Rakesh, Lesa Nelson, James W. Ogilvie, Hans Albertsen, & Kenneth Ward. (2015). Haplotypes at LBX1 Have Distinct Inheritance Patterns with Opposite Effects in Adolescent Idiopathic Scoliosis. PLoS ONE. 10(2). e0117708–e0117708. 26 indexed citations

Chettier, Rakesh, Hans Albertsen, & Kevin R. Ward. (2014). Next generation sequencing of families with endometriosis identifies new genomic regions likely to contribute to heritability. Fertility and Sterility. 102(3). e76–e77. 2 indexed citations

Chettier, Rakesh, Kenneth Ward, & Hans Albertsen. (2014). Endometriosis Is Associated with Rare Copy Number Variants. PLoS ONE. 9(8). e103968–e103968. 12 indexed citations

Albertsen, Hans, et al.. (2013). Genome-Wide Association Study Link Novel Loci to Endometriosis. PLoS ONE. 8(3). e58257–e58257. 115 indexed citations

Sweeney, Carol, Kenneth M. Boucher, Wade S. Samowitz, et al.. (2008). Oncogenetic tree model of somatic mutations and DNA methylation in colon tumors. Genes Chromosomes and Cancer. 48(1). 1–9. 31 indexed citations

Samowitz, Wade S., Martha L. Slattery, Carol Sweeney, et al.. (2007). APC Mutations and Other Genetic and Epigenetic Changes in Colon Cancer. Molecular Cancer Research. 5(2). 165–170. 114 indexed citations

Miyazaki, Shukichi, Akira Imatani, L. Ballard, et al.. (1997). The Chromosome Location of the Human Homolog of the Mouse Mammary Tumor-Associated GeneINT6and Its Status in Human Breast Carcinomas. Genomics. 46(1). 155–158. 37 indexed citations

Smith, Simon A., Jeff Stevens, Sylvie Mazoyer, et al.. (1996). Isolation of a Gene (DLG3) Encoding a Second Member of the Discs-Large Family on Chromosome 17q12–q21. Genomics. 31(2). 145–150. 31 indexed citations

10.

Thliveris, Andrew, Hans Albertsen, Thérèse M.F. Tuohy, et al.. (1996). Long-Range Physical Map and Deletion Characterization of the 1100-kbNotI Restriction Fragment Harboring theAPCGene. Genomics. 34(2). 268–270. 14 indexed citations

11.

Albertsen, Hans, Simon A. Smith, Roberta Melis, et al.. (1996). Sequence, Genomic Structure, and Chromosomal Assignment of Human DOC-2. Genomics. 33(2). 207–213. 38 indexed citations

12.

Albertsen, Hans, et al.. (1995). A collection of ordered tetranucleotide-repeat markers from the human genome. The American Journal of Human Genetics. 57(3). 46 indexed citations

13.

Smith, Simon A., et al.. (1995). Isolation and Mapping of a Gene Encoding a Novel Human ADP-Ribosylation Factor on Chromosome 17q12-q21. Genomics. 28(1). 113–115. 17 indexed citations

14.

Cropp, C S, Heli Nevanlinna, Seppo Pyrhönen, et al.. (1994). Evidence for involvement of BRCA1 in sporadic breast carcinomas.. PubMed. 54(10). 2548–51. 56 indexed citations

15.

Smith, Simon A., Richard A. DiCioccio, Jeffery P. Struewing, et al.. (1994). Localisation of the breast‐ovarian cancer susceptibility gene (BRCAI) on 17q12–21 to an interval of ⩽IcM. Genes Chromosomes and Cancer. 10(1). 71–76. 12 indexed citations

16.

Jorde, Lynn B., W. Scott Watkins, M. Carlson, et al.. (1994). Linkage disequilibrium predicts physical distance in the adenomatous polyposis coli region.. PubMed. 54(5). 884–98. 114 indexed citations

17.

Melis, Roberta, Paige K. Bradley, Tami Elsner, et al.. (1993). Polymorphic SSR (Simple-Sequence-Repeat) Markers for Chromosome 20. Genomics. 16(1). 56–62. 19 indexed citations

18.

Matsunami, Norisada, Brooke Smith, L. Ballard, et al.. (1992). Peripheral myelin protein–22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot–Marie–Tooth 1A. Nature Genetics. 1(3). 176–179. 246 indexed citations

19.

Albertsen, Hans, et al.. (1989). Improved control of partial DNA restriction enzyme digest in agarose using limiting concentrations of Mg^{+ +}. Nucleic Acids Research. 17(2). 808–808. 21 indexed citations

20.

Bolund, Lars, et al.. (1986). DNA probes for linkage analysis of X linked diseases: Localisation of the disease locus for anhidrotic ectodermal dysplasia. Clinical Genetics. 29(5). 458–458. 2 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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