Nelson B. Freimer

49.4k citations
127 papers · 8.0k · 3 hit papers · h-index 43

Impact in

  • Genetics top 0.5%
    • Genetic diversity and population structure
    • Genetic Associations and Epidemiology
    • Genetic and phenotypic traits in livestock
    • Genetic Mapping and Diversity in Plants and Animals
    • Neuroscience and Music Perception
    • Functional Brain Connectivity Studies

Papers in

    • Genetic Associations and Epidemiology 32
    • Genetic Mapping and Diversity in Plants and Animals 13
    • Genomic variations and chromosomal abnormalities 9
    • Genomics and Rare Diseases 7
    • Genetics and Neurodevelopmental Disorders 7

Nelson B. Freimer

123 papers receiving 7.7k citations

Nelson B. Freimer's Hit Papers

A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasis 1998 · 739 citations
7390+10+21Years since publication4008001.2k

Peers

Nelson B. Freimer
Comparison fields: 5 of 160
  • Genetics 2.8k
  • Cognitive Neuroscience 1.1k
  • Oncology 1.3k
  • Music 133
  • Hepatology 248
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Citations per field
00.5×10×13.3×
Stephen D. Smith · 1×
Citations per year

Countries citing papers authored by Nelson B. Freimer

Since Specialization
Citations

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

Fields of papers citing papers by Nelson B. Freimer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nelson B. Freimer. 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 Nelson B. Freimer. The network helps show where Nelson B. Freimer may publish in the future.

Co-authors

The 25 scholars most cited alongside Nelson B. Freimer, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Nelson B. Freimer Line = papers co-authored together Nelson B. Freimer links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 127 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Mutational processes of simple-sequence repeat loci in human populations.
Hit paper breakdown →
19941305
2
A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasis
Hit paper breakdown →
1998739
3
A gene encoding a P-type ATPase mutated in two forms of hereditary cholestasis
Hit paper breakdown →
1998532
4 1993489
5 1995271
6 2016258
7 1994243
8 1998211
9 2009160
10 2006158
11 1997131
12 2000126
13 2001124
14 2003117
15 2008111
16 2004105
17 2000103
18 199699
19 199590
20 200786

About Nelson B. Freimer

Nelson B. Freimer is a scholar working on Genetics, Molecular Biology, Surgery, Epidemiology and Clinical Psychology, having authored 127 papers that have together received 8.0k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (32 papers), Genetic Mapping and Diversity in Plants and Animals (13 papers), Genomic variations and chromosomal abnormalities (9 papers), Drug Transport and Resistance Mechanisms (8 papers), Pediatric Hepatobiliary Diseases and Treatments (8 papers), Genomics and Rare Diseases (7 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Obsessive-Compulsive Spectrum Disorders (6 papers). The work is most often cited by research in Genetics (2.8k citations), Cognitive Neuroscience (1.1k citations), Oncology (1.3k citations), Music (133 citations) and Hepatology (248 citations). Nelson B. Freimer has collaborated with scholars based in United States, United Kingdom and Poland. Frequent co-authors include Montgomery Slatkin, Ana M. Valdes, John Garza, Anna Di Rienzo, Amy Peterson, Susan K. Service, John Carlos Garza, Laura N. Bull, Chiara Sabatti and Siamak Baharloo. Their work appears in journals such as The American Journal of Human Genetics, Human Molecular Genetics, Nature Genetics, American Journal of Medical Genetics Part B Neuropsychiatric Genetics and Journal of Virology.

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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