Neal Clark

489 total citations
12 papers, 352 citations indexed

About

Neal Clark is a scholar working on Genetics, Cancer Research and Pathology and Forensic Medicine. According to data from OpenAlex, Neal Clark has authored 12 papers receiving a total of 352 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 6 papers in Cancer Research and 4 papers in Pathology and Forensic Medicine. Recurrent topics in Neal Clark's work include BRCA gene mutations in cancer (9 papers), Cancer Genomics and Diagnostics (6 papers) and Genetic factors in colorectal cancer (4 papers). Neal Clark is often cited by papers focused on BRCA gene mutations in cancer (9 papers), Cancer Genomics and Diagnostics (6 papers) and Genetic factors in colorectal cancer (4 papers). Neal Clark collaborates with scholars based in Norway, United Kingdom and Canada. Neal Clark's co-authors include Pål Møller, Lovise Mæhle, Jaran Apold, Anita Vabø, Astrid Stormorken, Anne Irene Hagen, Bent Fiane, Kjell Løvslett, Eli Marie Grindedal and Eivind Hovig and has published in prestigious journals such as Clinical Cancer Research, International Journal of Cancer and European Journal of Cancer.

In The Last Decade

Neal Clark

12 papers receiving 344 citations

Peers

Neal Clark

GENET

PFM

CR

ONCOL

MB

J. Gronwald Poland

Eli Marie Grindedal Norway

C. Crépin Netherlands

Kimberley Hill Canada

Mateja Krajc Slovenia

Esther Darder Spain

Sock Hoai Chan Singapore

Antoine Rousselin France

Jannet Blom Netherlands

Amal Yussuf United States

J. Gronwald Poland

Neal Clark

259 ×1.1

GENET

95 ×0.8

PFM

139 ×1.2

CR

187 ×1.8

ONCOL

124 ×1.5

MB

Citations per year, relative to Neal Clark Neal Clark (= 1×) peers J. Gronwald

Countries citing papers authored by Neal Clark

Since Specialization

Citations

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

Fields of papers citing papers by Neal Clark

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Neal Clark

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

All Works

Sort: Min cites: Since: Top N: Style:

12 of 12 papers shown

1.

Møller, Pål, Astrid Stormorken, Christoffer Jonsrud, et al.. (2013). Survival of patients with BRCA1-associated breast cancer diagnosed in an MRI-based surveillance program. Breast Cancer Research and Treatment. 139(1). 155–161. 38 indexed citations

2.

Møller, Pål, et al.. (2012). Age‐specific incidence rates for breast cancer in carriers of BRCA1 mutations from Norway. Clinical Genetics. 83(1). 88–91. 13 indexed citations

3.

Møller, Pål, Neal Clark, & Lovise Mæhle. (2011). A simplified method for segregation analysis (SISA) to determine penetrance and expression of a genetic variant in a family. Human Mutation. 32(5). 568–571. 14 indexed citations

4.

Møller, Pål & Neal Clark. (2011). CGEN-A clinical GENetics software application. Human Mutation. 32(5). 537–542. 3 indexed citations

5.

Møller, Pål, Lovise Mæhle, Lars Engebretsen, et al.. (2010). High penetrances of BRCA1 and BRCA2 mutations confirmed in a prospective series. Hereditary Cancer in Clinical Practice. 8(1). 2–2. 7 indexed citations

6.

Grindedal, Eli Marie, Pål Møller, Rosalind A. Eeles, et al.. (2009). Germ-Line Mutations in Mismatch Repair Genes Associated with Prostate Cancer. Cancer Epidemiology Biomarkers & Prevention. 18(9). 2460–2467. 78 indexed citations

7.

Grindedal, Eli Marie, Ignacio Blanco, Astrid Stormorken, et al.. (2008). High risk of endometrial cancer in colorectal cancer kindred is pathognomonic for MMR-mutation carriers. Familial Cancer. 8(2). 145–151. 11 indexed citations

8.

Mæhle, Lovise, Jaran Apold, Torbjørn Paulsen, et al.. (2008). High Risk for Ovarian Cancer in a Prospective Series Is Restricted to BRCA1/2 Mutation Carriers. Clinical Cancer Research. 14(22). 7569–7573. 16 indexed citations

9.

Møller, Pål, Lovise Mæhle, Neal Clark, & Jaran Apold. (2007). No Sib Pair Concordance for Breast or Ovarian Cancer in BRCA1 Mutation Carriers. Hereditary Cancer in Clinical Practice. 5(2). 67–67. 2 indexed citations

10.

Møller, Pål, D. Gareth Evans, Helen Gregory, et al.. (2007). Surveillance for familial breast cancer: Differences in outcome according to BRCA mutation status. International Journal of Cancer. 121(5). 1017–1020. 65 indexed citations

11.

Møller, Pål, Anne Irene Hagen, Jaran Apold, et al.. (2007). Genetic epidemiology of BRCA mutations – family history detects less than 50% of the mutation carriers. European Journal of Cancer. 43(11). 1713–1717. 94 indexed citations

12.

Stormorken, Astrid, Neal Clark, Eli Marie Grindedal, Lovise Mæhle, & Pål Møller. (2006). Prevention of colorectal cancer by colonoscopic surveillance in families with hereditary colorectal cancer. Scandinavian Journal of Gastroenterology. 42(5). 611–617. 11 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.

Explore authors with similar magnitude of impact