Jonathan L. Haines

91.2k total citations · 3 hit papers
412 papers, 21.3k citations indexed

About

Jonathan L. Haines is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Jonathan L. Haines has authored 412 papers receiving a total of 21.3k indexed citations (citations by other indexed papers that have themselves been cited), including 189 papers in Molecular Biology, 121 papers in Genetics and 102 papers in Physiology. Recurrent topics in Jonathan L. Haines's work include Alzheimer's disease research and treatments (79 papers), Retinal Diseases and Treatments (70 papers) and Genetic Associations and Epidemiology (63 papers). Jonathan L. Haines is often cited by papers focused on Alzheimer's disease research and treatments (79 papers), Retinal Diseases and Treatments (70 papers) and Genetic Associations and Epidemiology (63 papers). Jonathan L. Haines collaborates with scholars based in United States, United Kingdom and Netherlands. Jonathan L. Haines's co-authors include Margaret A. Pericak‐Vance, William K. Scott, James F. Gusella, John R. Gilbert, Silke Schmidt, Anita Agarwal, Jeffery M. Vance, Eric A. Postel, Michael A. Hauser and Paul J. Gallins and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Jonathan L. Haines

392 papers receiving 20.8k citations

Hit Papers

align trajectories sort by overperformance

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.

Complement Factor H Variant Increases the Risk of Age-Related Macular Degeneration

2005 1.9k citations Jonathan L. Haines, Michael A. Hauser et al. Science profile →
Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer disease

1994 1.4k citations Ann M. Saunders, P. A. Locke et al. profile →
Linkage of a Gene Causing Familial Amyotrophic Lateral Sclerosis to Chromosome 21 and Evidence of Genetic-Locus Heterogeneity

1991 278 citations Margaret A. Pericak‐Vance, Jonathan L. Haines et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jonathan L. Haines United States	75	8.4k	5.2k	4.2k	3.6k	3.1k	412	21.3k
Margaret A. Pericak‐Vance United States	63	7.0k 0.8×	4.8k 0.9×	3.6k 0.9×	2.8k 0.8×	2.9k 1.0×	340	18.4k
Lindsay A. Farrer United States	71	7.4k 0.9×	7.2k 1.4×	1.9k 0.5×	4.4k 1.2×	1.7k 0.6×	425	23.6k
Thomas Meitinger Germany	69	11.2k 1.3×	1.3k 0.2×	1.4k 0.3×	5.5k 1.5×	1.7k 0.5×	319	19.1k
Jeffery M. Vance United States	70	12.8k 1.5×	10.3k 2.0×	412 0.1×	4.4k 1.2×	4.2k 1.4×	298	29.0k
Heidi L. Rehm United States	53	13.8k 1.6×	1.9k 0.4×	761 0.2×	14.5k 4.0×	1.0k 0.3×	186	31.4k
Wayne W. Grody United States	45	11.9k 1.4×	1.9k 0.4×	600 0.1×	12.1k 3.4×	1.0k 0.3×	168	28.7k
Daniela Galimberti Italy	59	3.5k 0.4×	3.8k 0.7×	469 0.1×	690 0.2×	2.1k 0.7×	354	11.6k
Paul van der Valk Netherlands	80	5.8k 0.7×	1.6k 0.3×	532 0.1×	584 0.2×	2.1k 0.7×	252	19.5k
Allen D. Roses United States	77	14.4k 1.7×	17.9k 3.5×	296 0.1×	4.4k 1.2×	3.8k 1.2×	357	34.7k
Rafael Simó Spain	68	5.0k 0.6×	1.8k 0.3×	7.1k 1.7×	708 0.2×	456 0.1×	418	17.5k

Countries citing papers authored by Jonathan L. Haines

Since Specialization

Citations

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

Fields of papers citing papers by Jonathan L. Haines

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jonathan L. Haines

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Tosto, Giuseppe, Farid Rajabli, Rufus Akinyemi, et al.. (2025). Country-level incidence of Alzheimer disease and related dementias is associated with increased omega-6-PUFA consumption. Communications Medicine. 5(1). 326–326.

Byfield, Grace, Takiyah D. Starks, Christopher L. Edwards, et al.. (2023). Leveraging African American family connectors for Alzheimer's disease genomic studies. Alzheimer s & Dementia. 19(12). 5437–5446. 1 indexed citations

Corradetti, Giulia, Muneeswar Gupta Nittala, Dwight Stambolian, et al.. (2023). Assessment of intraretinal hyperreflective foci using multimodal imaging in eyes with age‐related macular degeneration. Acta Ophthalmologica. 102(1). e126–e132. 3 indexed citations

Naj, Adam C., Penelope Benchek, Logan Dumitrescu, et al.. (2023). A haptoglobin (HP) structural variant alters the effect of APOE alleles on Alzheimer's disease. Alzheimer s & Dementia. 19(11). 4886–4895. 5 indexed citations

Rong, Shi Song, Robert P. Igo, Jessica N. Cooke Bailey, et al.. (2020). Analysis of ATXN2 trinucleotide repeats in primary open angle glaucoma patients. Investigative Ophthalmology & Visual Science. 61(7). 1247–1247. 1 indexed citations

Darbar, Dawood, Prince J. Kannankeril, Brian S. Donahue, et al.. (2008). Cardiac Sodium Channel ( SCN5A ) Variants Associated with Atrial Fibrillation. Circulation. 117(15). 1927–1935. 249 indexed citations

Fan, Baojian, Louis R. Pasquale, Cynthia L. Grosskreutz, et al.. (2008). DNA sequence variants in the LOXL1 gene are associated with pseudoexfoliation glaucoma in a U.S. clinic-based population with broad ethnic diversity. BMC Medical Genetics. 9(1). 5–5. 93 indexed citations

Haines, Jonathan L., Michael A. Hauser, Silke Schmidt, et al.. (2005). Complement Factor H Variant Increases the Risk of Age-Related Macular Degeneration. Science. 308(5720). 419–421. 1898 indexed citations breakdown →

Sena, Dayse F, Louis R. Pasquale, R. Rand Allingham, et al.. (2004). Evaluation of NOS3 polymorphisms in patients with primary open angle glaucoma. Investigative Ophthalmology & Visual Science. 45(13). 4391–4391. 2 indexed citations

10.

Allingham, R. Rand, et al.. (2003). Optineurin Sequence Variants Do Not Predispose to Primary Open Angle Glaucoma. Investigative Ophthalmology & Visual Science. 44(13). 3227–3227. 3 indexed citations

11.

Oliveira, Sofia A., Eden R. Martin, William K. Scott, et al.. (2003). The Q7R Saitohin gene polymorphism is not associated with Alzheimer disease. Neuroscience Letters. 347(3). 143–146. 11 indexed citations

12.

Grubber, Janet M., Ann M. Saunders, William K. Scott, et al.. (1999). Analysis of association between Alzheimer disease and the K variant of butyrylcholinesterase (BCHE-K). Neuroscience Letters. 269(2). 115–119. 32 indexed citations

13.

Small, Gary W., Scott Komo, Asenath La Rue, et al.. (1996). Early Detection of Alzheimer's Disease by Combining Apolipoprotein E and Neuroimaginga. Annals of the New York Academy of Sciences. 802(1). 70–78. 43 indexed citations

14.

Short, M. Priscilla, Edward P. Richardson, Jonathan L. Haines, & David J. Kwiatkowski. (1995). Clinical, Neuropathological and Genetic Aspects of the Tuberous Sclerosis Complex. Brain Pathology. 5(2). 173–179. 40 indexed citations

15.

Wiggs, Janey L., et al.. (1994). Genetic Linkage of Autosomal Dominant Juvenile Glaucoma to 1q21-q31 in Three Affected Pedigrees. Genomics. 21(2). 299–303. 73 indexed citations

16.

Locke, P. A., Jonathan L. Haines, & Monica Ter‐Minassian. (1994). Methods for detecting additional genes underlying Alzheimer disease. The American Journal of Human Genetics. 55. 1 indexed citations

17.

Donaldson, Deirdre, D.R. Rosen, J. O'Regan, et al.. (1992). Two independent dinucleotide repeat polymorphisms at the D21S235 locus (21q22.1). Human Molecular Genetics. 1(8). 651–651. 2 indexed citations

18.

Kwiatkowski, David J., et al.. (1992). Construction of a GT polymorphism map of human 9q. Genomics. 12(2). 229–240. 147 indexed citations

19.

Haines, Jonathan L., Laurie J. Ozelius, Anil Menon, et al.. (1990). A genetic linkage map of chromosome 17. Genomics. 8(1). 1–6. 47 indexed citations

20.

Farrer, Lindsay A., et al.. (1985). Automating Data Manipulation for Genetic Analysis Using a Data Base Management System. Human Heredity. 35(5). 296–301. 9 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.

Explore authors with similar magnitude of impact