R. Mant

5.8k citations
19 papers · 3.9k · 1 hit paper · h-index 11

Impact in

Papers in

    • 14-3-3 protein interactions 2
    • Amyloidosis: Diagnosis, Treatment, Outcomes 2
    • Bioinformatics and Genomic Networks 2
    • Genetic Associations and Epidemiology 4
    • Genetics and Neurodevelopmental Disorders 3

R. Mant

19 papers receiving 3.8k citations

R. Mant's Hit Papers

Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease 1991 · 3.4k citations
3.4k0+11+23Years since publication10002.0k3.0k

Peers

R. Mant
Comparison fields: 5 of 102
  • Physiology 2.7k
  • Biological Psychiatry 138
  • Neurology 406
  • Cellular and Molecular Neuroscience 796
  • Psychiatry and Mental health 518
Replace L. Giuffra with:
L. Giuffra United States
A.D. Roses United States
N.G. Irving United Kingdom
Karen Rooke United States
Louise James United Kingdom
Andrew R. Haynes United Kingdom
Penelope Roques United Kingdom
Dieder Moechars Belgium
Liana Fidani Greece
Karin Axelman Sweden
R. Mant relative to L. Giuffra United States L. Giuffra's profile →
Citations per field
00.5×1.5×
L. Giuffra · 1×
Citations per year

Countries citing papers authored by R. Mant

Since Specialization
Citations

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

Fields of papers citing papers by R. Mant

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

19 of 19 papers shown
#Work
1
Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease
Hit paper breakdown →
19913446
2 1994146
3 199857
4
Polymerase chain reaction and restriction fragment length polymorphism mediated detection and speciation of Candida spp causing intraocular infection.
199844
5 199341
6
Linkage, association and mutational analysis of the dopamine D3 receptor gene in schizophrenia.
199637
7 199430
8 199324
9 199214
10 199914
11 199411
12 199510
13 19937
14 19964
15 19914
16 19933
17 19923
18
Susceptibility to schizophrenia and the dopamine d3 receptor gene
19932
19
Exclusion of close linkage between GABA a receptor subunit 1a gene and schizophrenia using a microsatellite repeat marker
19911

About R. Mant

R. Mant is a scholar working on Molecular Biology, Genetics, Physiology, Cognitive Neuroscience and Pharmacology, having authored 19 papers that have together received 3.9k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (4 papers), Alzheimer's disease research and treatments (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), 14-3-3 protein interactions (2 papers), Amyloidosis: Diagnosis, Treatment, Outcomes (2 papers), Autism Spectrum Disorder Research (2 papers), Bioinformatics and Genomic Networks (2 papers) and Folate and B Vitamins Research (1 paper). The work is most often cited by research in Physiology (2.7k citations), Biological Psychiatry (138 citations), Neurology (406 citations), Cellular and Molecular Neuroscience (796 citations) and Psychiatry and Mental health (518 citations). R. Mant has collaborated with scholars based in United Kingdom, Japan and United States. Frequent co-authors include Mike Owen, Fiona Crawford, Alison Goate, John Hardy, Penelope Roques, N.G. Irving, Karen Rooke, Marie‐Christine Chartier‐Harlin, Martin N. Rossor and Jeremy Brown. Their work appears in journals such as Molecular Psychiatry, Journal of Medical Genetics, Human Genetics, Nature and Psychological Medicine.

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