L. Giuffra

6.2k citations
25 papers · 4.6k · 1 hit paper · h-index 13

Impact in

Papers in

    • Genetic Associations and Epidemiology 7
    • Genomics and Rare Diseases 3
    • Genetic Mapping and Diversity in Plants and Animals 3
    • Genetics and Neurodevelopmental Disorders 2
    • Genetic and phenotypic traits in livestock 2
    • 14-3-3 protein interactions 2

L. Giuffra

22 papers receiving 4.3k citations

L. Giuffra's Hit Papers

Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease 1991 · 3.7k citations
3.7k0+11+23Years since publication10002.0k3.0k

Peers

L. Giuffra
Comparison fields: 5 of 115
  • Physiology 2.9k
  • Biological Psychiatry 151
  • Neurology 509
  • Cellular and Molecular Neuroscience 800
  • Pharmacology 684
Replace R. Mant with:
R. Mant United Kingdom
Karen Rooke United States
A.D. Roses United States
N.G. Irving United Kingdom
Andrew R. Haynes United Kingdom
Donna Romano United States
Penelope Roques United Kingdom
Ellen Nemens United States
Dominique Campion France
Liana Fidani Greece
L. Giuffra relative to R. Mant United Kingdom R. Mant's profile →
Citations per field
00.5×1.5×
R. Mant · 1×
Citations per year

Countries citing papers authored by L. Giuffra

Since Specialization
Citations

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

Fields of papers citing papers by L. Giuffra

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 25 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease
Hit paper breakdown →
19913699
2 1988319
3 1992163
4 199484
5 199360
6 201357
7 199439
8 201228
9 198923
10 199121
11
Linkage and mode of inheritance in complex traits.
198920
12 198916
13
Age of onset, gender and severity in obsessive-compulsive disorder. A study on a mexican population
199713
14 199210
15 19907
16
The Opioid Crisis in Missouri: A Call to Action for Physicians, Legislators, and Society.
20197
17 19925
18 19904
19 20003
20 19912

About L. Giuffra

L. Giuffra is a scholar working on Genetics, Molecular Biology, Physiology, Psychiatry and Mental health and Surgery, having authored 25 papers that have together received 4.6k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (7 papers), Genomics and Rare Diseases (3 papers), Genetic Mapping and Diversity in Plants and Animals (3 papers), Alzheimer's disease research and treatments (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), 14-3-3 protein interactions (2 papers), Genetic and phenotypic traits in livestock (2 papers) and Autism Spectrum Disorder Research (2 papers). The work is most often cited by research in Physiology (2.9k citations), Biological Psychiatry (151 citations), Neurology (509 citations), Cellular and Molecular Neuroscience (800 citations) and Pharmacology (684 citations). L. Giuffra has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Liana Fidani, Chris J. Talbot, Jeremy Brown, Louise James, Margaret A. Pericak‐Vance, John Hardy, Fiona Crawford, Karen Rooke, Penelope Roques and Marie‐Christine Chartier‐Harlin. Their work appears in journals such as Journal of the American Society of Nephrology, Nature, Genomics, Human Heredity and International Review of Psychiatry.

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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