M. Hoff

649 citations
37 papers · 531 · h-index 12

Impact in

  • Genetics top 10%
    • Genetics and Neurodevelopmental Disorders
    • Genetic Associations and Epidemiology
    • Genomic variations and chromosomal abnormalities

Papers in

    • DNA and Nucleic Acid Chemistry 6
    • DNA Repair Mechanisms 5
    • Epigenetics and DNA Methylation 3
    • Genomic variations and chromosomal abnormalities 6
    • Genetic Associations and Epidemiology 5
    • Genetics and Neurodevelopmental Disorders 4
    • Digestive system and related health 3

M. Hoff

36 papers receiving 502 citations

Peers

M. Hoff
Comparison fields: 5 of 59
  • Genetics 271
  • Biological Psychiatry 18
  • Cellular and Molecular Neuroscience 119
  • Psychiatry and Mental health 77
  • Molecular Biology 210
Replace Mina Ohadi with:
Mina Ohadi Iran
Lisa E. Esterling United States
S. Christie United Kingdom
Shaomin Zhu China
Suneeta Madan‐Khetarpal United States
Karen Gentile United States
Nick Jacobsen United Kingdom
Susan J. Donohue United States
Elisabeth Gabau Spain
M. Kron United States
M. Hoff relative to Mina Ohadi Iran Mina Ohadi's profile →
Citations per field
00.5×1.5×
Mina Ohadi · 1×
Citations per year

Countries citing papers authored by M. Hoff

Since Specialization
Citations

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

Fields of papers citing papers by M. Hoff

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside M. Hoff, 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 M. Hoff Line = papers co-authored together M. Hoff links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 37 papers — load more, or switch the sort, to bring in the rest.

#Work
1 1987107
2 199863
3 199648
4 199248
5 199535
6
Further linkage data on cystic fibrosis: the Utah Study.
198634
7 199224
8 199621
9 199414
10 199413
11 199413
12 199513
13 198811
14 19888
15 19938
16 19877
17 19957
18 19946
19 19946
20 19885

About M. Hoff

M. Hoff is a scholar working on Molecular Biology, Genetics, Psychiatry and Mental health, Cellular and Molecular Neuroscience and Physiology, having authored 37 papers that have together received 531 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (6 papers), DNA and Nucleic Acid Chemistry (6 papers), DNA Repair Mechanisms (5 papers), Genetic Associations and Epidemiology (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), Bipolar Disorder and Treatment (3 papers), Epigenetics and DNA Methylation (3 papers) and Digestive system and related health (3 papers). The work is most often cited by research in Genetics (271 citations), Biological Psychiatry (18 citations), Cellular and Molecular Neuroscience (119 citations), Psychiatry and Mental health (77 citations) and Molecular Biology (210 citations). M. Hoff has collaborated with scholars based in United States, Germany and Belgium. Frequent co-authors include John Holik, Hilary Coon, Paul H. Wender, Fred Reimherr, William Byerley, M. Leppert, P. O’Connell, Yusuke Nakamura, G.M. Lathrop and Marina Myles‐Worsley. Their work appears in journals such as Nucleic Acids Research, Psychiatric Genetics, Human Heredity, Biological Psychiatry and Human Molecular Genetics.

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