K Berg

745 total citations
11 papers, 339 citations indexed

About

K Berg is a scholar working on Genetics, Psychiatry and Mental health and Molecular Biology. According to data from OpenAlex, K Berg has authored 11 papers receiving a total of 339 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 4 papers in Psychiatry and Mental health and 2 papers in Molecular Biology. Recurrent topics in K Berg's work include Attention Deficit Hyperactivity Disorder (2 papers), Congenital Heart Disease Studies (2 papers) and Congenital heart defects research (2 papers). K Berg is often cited by papers focused on Attention Deficit Hyperactivity Disorder (2 papers), Congenital Heart Disease Studies (2 papers) and Congenital heart defects research (2 papers). K Berg collaborates with scholars based in United States, Colombia and Norway. K Berg's co-authors include Marit Hornberg Solaas, Linda A. Corey, W. E. Nance, John M. Pellock, Robert J. DeLorenzo, A L Børresen, W E Nance, Joan E. Bailey‐Wilson, F. Xavier Castellanos and David Pineda and has published in prestigious journals such as Neurology, Psychological Medicine and Molecular Psychiatry.

In The Last Decade

K Berg

11 papers receiving 323 citations

Peers

K Berg
K Berg
Citations per year, relative to K Berg K Berg (= 1×) peers Amira Masri

Countries citing papers authored by K Berg

Since Specialization
Citations

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

Fields of papers citing papers by K Berg

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of K Berg

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

All Works

11 of 11 papers shown
1.
Arcos‐Burgos, Mauricio, F. Xavier Castellanos, David Konecki, et al.. (2004). Pedigree disequilibrium test (PDT) replicates association and linkage between DRD4 and ADHD in multigenerational and extended pedigrees from a genetic isolate. Molecular Psychiatry. 9(3). 252–259. 52 indexed citations
2.
Ahaghotu, Chiledum, Agnes Baffoe‐Bonnie, Rick A. Kittles, et al.. (2004). Clinical characteristics of African-American men with hereditary prostate cancer: the AAHPC study. Prostate Cancer and Prostatic Diseases. 7(2). 165–169. 16 indexed citations
3.
Arcos‐Burgos, Mauricio, F. Xavier Castellanos, Francisco Lopera, et al.. (2002). Attention‐deficit/hyperactivity disorder (ADHD): feasibility of linkage analysis in a genetic isolate using extended and multigenerational pedigrees. Clinical Genetics. 61(5). 335–343. 25 indexed citations
4.
Faraone, Stephen V., Mary C. Blehar, John Pepple, et al.. (1996). Diagnostic accuracy and confusability analyses: an application to the Diagnostic Interview for Genetic Studies. Psychological Medicine. 26(2). 401–410. 67 indexed citations
5.
Corey, Linda A., K Berg, Marit Hornberg Solaas, & W E Nance. (1992). The epidemiology of pregnancy complications and outcome in a Norwegian twin population.. PubMed. 80(6). 989–94. 33 indexed citations
6.
Corey, Linda A., K Berg, John M. Pellock, et al.. (1991). The occurrence of epilepsy and febrile seizures in Virginian and Norwegian twins. Neurology. 41(9). 1433–1433. 76 indexed citations
7.
Møller, Pål, Narve Moe, Ola Didrik Saugstad, et al.. (1990). Spinal muscular atrophy type I combined with atrial septal defect in three sibs. Clinical Genetics. 38(2). 81–83. 30 indexed citations
8.
Boughman, Joann A., Jacqueline Astemborski, K Berg, E. B. Clark, & C Ferencz. (1988). Variation in Expression of Congenital Cardiovascular Malformations within and Among Families. PubMed. 43. 93–103. 6 indexed citations
9.
Tsipouras, Petros, et al.. (1986). Marfan syndrome: exclusion of genetic linkage to the COL1A2 gene.. PubMed. 30(5). 428–32. 30 indexed citations
10.
Berg, K. (1978). Genetic linkage as a cause of clinical variation in inherited disorders. Cytogenetic and Genome Research. 22(1-6). 618–620. 1 indexed citations
11.
Pronko, N. H., et al.. (1960). Twenty years of shock therapy in America. 1937-1956: an annotated bibliography.. PubMed. 62. 233–329. 3 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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