Friedrik P. Wikman

1.1k total citations
26 papers, 739 citations indexed

About

Friedrik P. Wikman is a scholar working on Pathology and Forensic Medicine, Molecular Biology and Oncology. According to data from OpenAlex, Friedrik P. Wikman has authored 26 papers receiving a total of 739 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Pathology and Forensic Medicine, 13 papers in Molecular Biology and 12 papers in Oncology. Recurrent topics in Friedrik P. Wikman's work include Genetic factors in colorectal cancer (14 papers), Cancer Genomics and Diagnostics (10 papers) and Colorectal Cancer Screening and Detection (7 papers). Friedrik P. Wikman is often cited by papers focused on Genetic factors in colorectal cancer (14 papers), Cancer Genomics and Diagnostics (10 papers) and Colorectal Cancer Screening and Detection (7 papers). Friedrik P. Wikman collaborates with scholars based in Denmark, United States and Sweden. Friedrik P. Wikman's co-authors include Torben F. Ørntoft, Brian F.C. Clark, Ming-Lan Lu, Carlos Cordon‐Cardo, Søren Laurberg, Gunhild E. Siboska, Hans Uffe Petersen, Niels Katballe, Torben F. Ørntoft and Mariann Christensen and has published in prestigious journals such as Nucleic Acids Research, The EMBO Journal and Bioinformatics.

In The Last Decade

Friedrik P. Wikman

26 papers receiving 718 citations

Peers

Countries citing papers authored by Friedrik P. Wikman

Since Specialization

Citations

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

Fields of papers citing papers by Friedrik P. Wikman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Friedrik P. Wikman. 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 Friedrik P. Wikman. The network helps show where Friedrik P. Wikman may publish in the future.

Co-authorship network of co-authors of Friedrik P. Wikman

This figure shows the co-authorship network connecting the top 25 collaborators of Friedrik P. Wikman. A scholar is included among the top collaborators of Friedrik P. Wikman 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 Friedrik P. Wikman. Friedrik P. Wikman 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

#	Work	Indexed citations
1	New Pathogenic Germline Variants in Very Early Onset and Familial Colorectal Cancer Patients 2020 ·Frontiers in Genetics ·(unknown), Majbritt Busk Madsen, Jane Hübertz Frederiksen, Lukas Adrian Berchtold, Christina Therkildsen, Gro Linno Willemoe, Jane P. Hasselby, Friedrik P. Wikman, Henrik Okkels, Anne‐Bine Skytte, Mef Nilbert, Karin Wadt, Anne‐Marie Gerdes, Thomas van Overeem Hansen	19
2	Detection of PMS2 Mutations by Screening Hereditary Nonpolyposis Colon Cancer Families from Denmark and Sweden 2019 ·Genetic Testing and Molecular Biomarkers ·Henrik Okkels, Kristina Lagerstedt‐Robinson, Friedrik P. Wikman, Thomas van Overeem Hansen, Ihab Bishara Yousef Lolas, (unknown), Henrik Krarup	3
3	Functional examination of MLH1, MSH2, and MSH6 intronic mutations identified in Danish colorectal cancer patients 2013 ·BMC Medical Genetics ·(unknown), (unknown), Lene Juel Rasmussen, Anne‐Marie Gerdes, Lotte Krogh, Inge Bernstein, Henrik Okkels, Friedrik P. Wikman, Finn C. Nielsen, Thomas van Overeem Hansen	18
4	Frequent genomic loss at chr16p13.2 is associated with poor prognosis in colorectal cancer 2010 ·International Journal of Cancer ·Claus L. Andersen, Philippe Lamy, Kasper Thorsen, Eigil Kjeldsen, Friedrik P. Wikman, Palle Villesen, Bodil Øster, Søren Laurberg, Torben F. Ørntoft	27
5	Functional characterization of rare missense mutations in MLH1 and MSH2 identified in Danish colorectal cancer patients 2009 ·Familial Cancer ·Lise Lotte Christensen, Reetta Kariola, Mari Korhonen, Friedrik P. Wikman, Lone Sunde, Anne‐Marie Gerdes, Henrik Okkels, (unknown), Inge Bernstein, Thomas van Overeem Hansen, Rikke Hagemann‐Madsen, Claus L. Andersen, Minna Nyström, Torben F. Ørntoft	6
6	Major contribution from recurrent alterations and MSH6 mutations in the Danish Lynch syndrome population 2008 ·Familial Cancer ·Mef Nilbert, Friedrik P. Wikman, Thomas van Overeem Hansen, Henrik Krarup, Torben F. Ørntoft, Finn Cilius Nielsen, Lone Sunde, Anne‐Marie Gerdes, Dorthe Gylling Crüger, Susanne Timshel, (unknown), Inge Bernstein, Henrik Okkels	33
7	BRCA1 and BRCA2 mutations in Danish families with hereditary breast and/or ovarian cancer 2008 ·Acta Oncologica ·Mads Thomassen, Thomas van Overeem Hansen, Åke Borg, (unknown), Friedrik P. Wikman, Inge Søkilde Pedersen, Marie Luise Bisgaard, Finn C. Nielsen, Torben A. Kruse, Anne‐Marie Gerdes	36
8	The association between genetic variants in hMLH1 and hMSH2 and the development of sporadic colorectal cancer in the Danish population 2008 ·BMC Medical Genetics ·(unknown), Bo Eskerod Madsen, Friedrik P. Wikman, Carsten Wiuf, Karen Koed, Anne Tjønneland, Anja Olsen, Ann‐Christine Syvänen, Claus L. Andersen, Torben F. Ørntoft	15
9	A genome‐wide linkage search for bipolar disorder susceptibility loci in a large and complex pedigree from the eastern part of Cuba 2006 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Beatríz Marcheco Teruel, Tracey Flint, Friedrik P. Wikman, (unknown), Luís Miguel González, Lourdes Blanco, Qihua Tan, H. Ewald, Torben Ørntoft, (unknown), Anders D. Børglum, Ole Mors	21
10	Genotyping and annotation of Affymetrix SNP arrays 2006 ·Nucleic Acids Research ·Philippe Lamy, Claus L. Andersen, Friedrik P. Wikman, Carsten Wiuf	15
11	High-Density Single Nucleotide Polymorphism Array Defines Novel Stage and Location-Dependent Allelic Imbalances in Human Bladder Tumors 2005 ·Cancer Research ·Karen Koed, Carsten Wiuf, Lise-Lotte Christensen, Friedrik P. Wikman, Karsten Zieger, (unknown), Hans von der Maase, Torben F. Ørntoft	68
12	Presymptomatic diagnosis using a deletion of a single codon in families with hereditary non-polyposis colorectal cancer 2004 ·Mutation research. Fundamental and molecular mechanisms of mutagenesis ·R Ripa, Niels Katballe, Friedrik P. Wikman, Anne Charlotte Jäger, Inge Bernstein, Torben Ørntoft, Marianne Schwartz, Finn Cilius Nielsen, Marie Luise Bisgaard	6
13	A genome‐wide search for risk genes using homozygosity mapping and microarrays with 1,494 single‐nucleotide polymorphisms in 22 eastern Cuban families with bipolar disorder 2004 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·H. Ewald, Friedrik P. Wikman, Beatríz Marcheco Teruel, Henriette N. Buttenschøn, Manolito Torralba, Thomas D. Als, (unknown), Tracey Flint, Tove H. Jorgensen, Lourdes Blanco, Torben A. Kruse, Torben F. Ørntoft, Ole Mors	18
14	Antibody‐based screening for hereditary nonpolyposis colorectal carcinoma compared with microsatellite analysis and sequencing 2002 ·Cancer ·Mariann Christensen, Niels Katballe, Friedrik P. Wikman, Hanne Primdahl, Flemming Brandt Sørensen, Søren Laurberg, Torben F. Ørntoft	45
15	Neural network predicts sequence of TP53 gene based on DNA chip 2002 ·Bioinformatics ·(unknown), Friedrik P. Wikman, Ming-Lan Lu, Carlos Cordon‐Cardo, Christopher T. Workman, Torben F. Ørntoft, Søren Brunak, Steen Knudsen	8
16	Impact of alterations affecting the p53 pathway in bladder cancer on clinical outcome, assessed by conventional and array-based methods. 2002 ·PubMed ·Ming-Lan Lu, Friedrik P. Wikman, Torben F. Ørntoft, Elizabeth Charytonowicz, Farhang Rabbani, Zuo‐Feng Zhang, Guido Dalbagni, Kamal S. Pohar, Guo-Pei Yu, Carlos Cordon‐Cardo	116
17	Efficient Mutation Detection in Mismatch Repair Genes Using a Combination of Single-Strand Conformational Polymorphism and Heteroduplex Analysis at a Controlled Temperature 2000 ·Genetic Testing ·Friedrik P. Wikman, Niels Katballe, Mariann Christensen, Søren Laurberg, Torben F. Ørntoft	8
18	Crosslinking of tRNA containing a long extra arm to elongation factor Tu bytrans-diamminedichloroplatinum(II) 1990 ·Nucleic Acids Research ·(unknown), Friedrik P. Wikman, Brian F.C. Clark	8
19	Crosslinking of elongation factor Tm to tRNA^Pheby trans-diamminedichloroplatinum (II). Characterization of two crosslinking sites in the tRNA 1987 ·Nucleic Acids Research ·Friedrik P. Wikman, Pascale Romby, (unknown), Brian F.C. Clark, J.P. Ebel, Chantal Ehresmann, Bernard Ehresmann	20
20	Different conformations of tRNA in the ribosomal P‐site and A‐site 1985 ·European Journal of Biochemistry ·(unknown), Gunhild E. Siboska, Friedrik P. Wikman, Brian F.C. Clark	17

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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