Mark Hoff

4.4k total citations · 2 hit papers
21 papers, 2.4k citations indexed

About

Mark Hoff is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Mark Hoff has authored 21 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 9 papers in Molecular Biology and 4 papers in Psychiatry and Mental health. Recurrent topics in Mark Hoff's work include Genetics and Neurodevelopmental Disorders (8 papers), Genetic Associations and Epidemiology (6 papers) and Genomic variations and chromosomal abnormalities (6 papers). Mark Hoff is often cited by papers focused on Genetics and Neurodevelopmental Disorders (8 papers), Genetic Associations and Epidemiology (6 papers) and Genomic variations and chromosomal abnormalities (6 papers). Mark Hoff collaborates with scholars based in United States, Sweden and Italy. Mark Hoff's co-authors include Mark Leppert, R. White, P. O’Connell, Tom Holm, Yusuke Nakamura, Cindy M. Martin, E. Fujimoto, Melanie Culver, Roger K. Wolff and Hilary Coon and has published in prestigious journals such as Nature, Science and Nucleic Acids Research.

In The Last Decade

Mark Hoff

20 papers receiving 2.3k citations

Hit Papers

Variable Number of Tandem Repeat (VNTR) Markers for Human... 1985 2026 1998 2012 1987 1985 400 800 1.2k
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.

  1. Variable Number of Tandem Repeat (VNTR) Markers for Human Gene Mapping
    1987 1.3k citations Yusuke Nakamura, Mark Leppert et al. Science profile →
  2. A closely linked genetic marker for cystic fibrosis
    1985 372 citations R. White, Mark Leppert et al. profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mark Hoff United States 13 1.2k 1.2k 254 240 236 21 2.4k
Sabine Fauré France 7 1.9k 1.6× 1.1k 1.0× 272 1.1× 95 0.4× 314 1.3× 10 3.3k
James Ireland United States 11 1.4k 1.2× 1.4k 1.2× 189 0.7× 54 0.2× 136 0.6× 13 2.8k
H H Kazazian United States 32 1.7k 1.4× 857 0.7× 195 0.8× 113 0.5× 90 0.4× 64 3.2k
Golder N. Wilson United States 29 1.8k 1.5× 1.3k 1.1× 428 1.7× 81 0.3× 139 0.6× 117 3.1k
Karen Oliver Australia 20 908 0.8× 589 0.5× 221 0.9× 76 0.3× 278 1.2× 50 1.9k
Vivien J. Bubb United Kingdom 27 1.6k 1.3× 918 0.8× 222 0.9× 132 0.6× 510 2.2× 84 3.5k
Wenli Gu China 22 1.4k 1.2× 1.3k 1.1× 459 1.8× 95 0.4× 372 1.6× 47 2.7k
Alan Y. Sakaguchi United States 18 2.0k 1.6× 915 0.8× 123 0.5× 95 0.4× 891 3.8× 39 3.5k
Daniela T. Pilz United Kingdom 33 1.8k 1.5× 1.6k 1.4× 98 0.4× 89 0.4× 437 1.9× 72 3.6k
Paula E. May United States 18 1.7k 1.4× 1.7k 1.5× 575 2.3× 108 0.5× 224 0.9× 37 3.5k

Countries citing papers authored by Mark Hoff

Since Specialization
Citations

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

Fields of papers citing papers by Mark Hoff

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mark Hoff

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

All Works

20 of 20 papers shown
1.
Myles‐Worsley, Marina, Hilary Coon, Jennifer E. McDowell, et al.. (1999). Linkage of a composite inhibitory phenotype to a chromosome 22q locus in eight Utah families. American Journal of Medical Genetics. 88(5). 544–550. 76 indexed citations
2.
Coon, Hilary, Jennifer E. McDowell, Colleen A. Brenner, et al.. (1999). Linkage of a composite inhibitory phenotype to a chromosome 22q locus in eight Utah families. American Journal of Medical Genetics. 88(5). 544–550. 5 indexed citations
3.
Byerley, William, Mark Hoff, John Holik, et al.. (1995). Linkage Analysis between Schizophrenia and Index Simple-Sequence Repeat Loci for Chromosome 21. Human Heredity. 45(1). 49–52. 6 indexed citations
4.
Coon, Hilary, et al.. (1995). Mutation scan of the D1 dopamine receptor gene in 22 cases of bipolar I disorder. American Journal of Medical Genetics. 60(2). 150–153. 12 indexed citations
5.
Byerley, William, John Holik, Mark Hoff, & Hilary Coon. (1995). Search for a gene predisposing to manic‐depression on chromosome 21. American Journal of Medical Genetics. 60(3). 231–233. 15 indexed citations
6.
Coon, Hilary, John Holik, Mark Hoff, et al.. (1994). Analysis of chromosome 22 markers in nine schizophrenia pedigrees. American Journal of Medical Genetics. 54(1). 72–79. 104 indexed citations
7.
Coon, Hilary, Steven Jensen, John Holik, et al.. (1994). Genomic scan for genes predisposing to schizophrenia. American Journal of Medical Genetics. 54(1). 59–71. 132 indexed citations
8.
Polymeropoulos, Mihael H., Hilary Coon, William Byerley, et al.. (1994). Search for a schizophrenia susceptibility locus on human chromosome 22. American Journal of Medical Genetics. 54(2). 93–99. 63 indexed citations
9.
Kasapi, Melpomeni, et al.. (1994). SSCP at the HTR1DA locus. Human Molecular Genetics. 3(8). 1444–1444. 3 indexed citations
10.
Coon, Hilary, Rosemarie Plaetke, John Holik, et al.. (1993). Use of a neurophysiological trait in linkage analysis of schizophrenia. Biological Psychiatry. 34(5). 277–289. 50 indexed citations
11.
Jensen, Steven, Rosemarie Plaetke, John Holik, et al.. (1993). Linkage Analysis of Schizophrenia: The D1 Dopamine Receptor Gene and Several Flanking DNA Markers. Human Heredity. 43(1). 58–62. 12 indexed citations
12.
Byerley, William, Mark Hoff, John Holik, Marc G. Caron, & Bruno Giros. (1993). VNTR polymorphism for the human dopamine transporter gene (DAT1). Human Molecular Genetics. 2(3). 335–335. 29 indexed citations
13.
Coon, Hilary, Mark Hoff, John Holik, et al.. (1993). C to T nucleotide substitution in codon 713 of amyloid precursor protein gene not found in 86 unrelated schizophrenics from multiplex families. American Journal of Medical Genetics. 48(1). 36–39. 8 indexed citations
14.
Byerley, William, Hilary Coon, Mark Hoff, et al.. (1993). Human Dopamine Transporter Gene Not Linked to Schizophrenia in Multigenerational Pedigrees. Human Heredity. 43(5). 319–322. 33 indexed citations
15.
Byerley, William, Akbar S. Khan, John Holik, Mark Hoff, & James M. Sikela. (1993). Dinucleotide repeat polymorphism in the 3'untranslated region of an anonymous brain cDNA mapping to chromosome 2 (D2S230). Human Molecular Genetics. 2(8). 1329–1329.
16.
Byerley, William, John Holik, Mark Hoff, et al.. (1993). Strategies to identify genes for complex diseases. Schizophrenia Research. 9(2-3). 115–115. 1 indexed citations
17.
Coon, Hilary, William Byerley, John Holik, et al.. (1993). Linkage analysis of schizophrenia with five dopamine receptor genes in nine pedigrees.. PubMed. 52(2). 327–34. 75 indexed citations
18.
Coon, Hilary, Steve Jensen, Mark Hoff, et al.. (1993). A genome-wide search for genes predisposing to manic-depression, assuming autosomal dominant inheritance.. PubMed. 52(6). 1234–49. 61 indexed citations
19.
Nakamura, Yusuke, Mark Leppert, P. O’Connell, et al.. (1987). Variable Number of Tandem Repeat (VNTR) Markers for Human Gene Mapping. Science. 235(4796). 1616–1622. 1315 indexed citations breakdown →
20.
Barker, David G., Mark Hoff, Arnold Oliphant, & R. White. (1984). A second type II restriction endonuclease fromThermus aquaticuswith an unusual sequence specificity. Nucleic Acids Research. 12(14). 5567–5581. 26 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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