J. L. Haines

4.9k total citations
45 papers, 1.3k citations indexed

About

J. L. Haines is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, J. L. Haines has authored 45 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 15 papers in Genetics and 9 papers in Physiology. Recurrent topics in J. L. Haines's work include Genetics and Neurodevelopmental Disorders (7 papers), Genetic Associations and Epidemiology (6 papers) and Alzheimer's disease research and treatments (6 papers). J. L. Haines is often cited by papers focused on Genetics and Neurodevelopmental Disorders (7 papers), Genetic Associations and Epidemiology (6 papers) and Alzheimer's disease research and treatments (6 papers). J. L. Haines collaborates with scholars based in United States, Canada and United Kingdom. J. L. Haines's co-authors include M. A. Pericak‐Vance, James F. Gusella, Jeffery M. Vance, William K. Scott, Nathalie Schnetz‐Boutaud, Monica A. De La Paz, Felicia Lennon, Margaret A. Pericak‐Vance, Margaret A. Pericak‐Vance and Lisa F. Barcellos and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Neurology.

In The Last Decade

J. L. Haines

43 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
J. L. Haines United States 18 590 322 295 229 191 45 1.3k
Nobushige Tanaka Japan 12 544 0.9× 128 0.4× 116 0.4× 135 0.6× 85 0.4× 19 1.4k
Bernd Rautenstrauß Germany 26 747 1.3× 114 0.4× 224 0.8× 389 1.7× 53 0.3× 90 1.8k
Elsebet Østergaard Denmark 26 1.6k 2.7× 158 0.5× 298 1.0× 70 0.3× 55 0.3× 67 2.2k
Arnold Munnich France 25 1.6k 2.8× 96 0.3× 580 2.0× 237 1.0× 56 0.3× 55 2.3k
Galina Dvoriantchikova United States 26 1.1k 1.9× 219 0.7× 44 0.1× 492 2.1× 300 1.6× 52 1.9k
R. H. M. King United Kingdom 31 742 1.3× 390 1.2× 104 0.4× 53 0.2× 132 0.7× 79 2.4k
Inge Van Hove Belgium 22 596 1.0× 143 0.4× 50 0.2× 477 2.1× 85 0.4× 38 1.4k
Patrizia Amati‐Bonneau France 34 2.7k 4.5× 231 0.7× 269 0.9× 329 1.4× 286 1.5× 72 3.3k
Allan R. Shepard United States 18 775 1.3× 105 0.3× 168 0.6× 752 3.3× 48 0.3× 38 1.4k
Michele Pinelli Italy 19 745 1.3× 144 0.4× 457 1.5× 56 0.2× 55 0.3× 49 1.3k

Countries citing papers authored by J. L. Haines

Since Specialization
Citations

This map shows the geographic impact of J. 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 J. 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 J. L. Haines more than expected).

Fields of papers citing papers by J. L. Haines

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

This figure shows the co-authorship network connecting the top 25 collaborators of J. L. Haines. A scholar is included among the top collaborators of J. 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 J. L. Haines. J. L. Haines 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.
Tong, Tong, Congcong Zhu, John J. Farrell, et al.. (2024). Blood-derived mitochondrial DNA copy number is associated with Alzheimer disease, Alzheimer-related biomarkers and serum metabolites. Alzheimer s Research & Therapy. 16(1). 234–234. 9 indexed citations
2.
Zuvich, Rebecca L., Yvonne M. Bradford, S J Kenealy, et al.. (2009). Follow-up examination of linkage and association to chromosome 1q43 in multiple sclerosis. Genes and Immunity. 10(7). 624–630. 7 indexed citations
3.
Wagner, Sören, et al.. (2005). A Second Locus for Pigment Dispersion Syndrome Maps to Chromosome 18q21. Investigative Ophthalmology & Visual Science. 46(13). 29–29. 5 indexed citations
4.
Kenealy, S J, Yvonne M. Bradford, Nathalie Schnetz‐Boutaud, et al.. (2005). Examination of seven candidate regions for multiple sclerosis: strong evidence of linkage to chromosome 1q44. Genes and Immunity. 7(1). 73–76. 10 indexed citations
5.
Kenealy, S J, Marie‐Claude Babron, Yvonne M. Bradford, et al.. (2004). A Second-Generation Genomic Screen for Multiple Sclerosis. The American Journal of Human Genetics. 75(6). 1070–1078. 40 indexed citations
6.
Wiggs, Janey L., et al.. (2004). A genomewide scan identifies novel early-onset primary open-angle glaucoma loci on 9q22 and 20p12. American Journal of Ophthalmology. 138(4). 704–704. 5 indexed citations
7.
Haines, J. L., Lisa F. Barcellos, Margaret A. Pericak‐Vance, et al.. (2001). Linkage and association analysis of chromosome 19q13 in multiple sclerosis. Neurogenetics. 3(4). 195–201. 28 indexed citations
8.
Vance, Jeffery M., Larry H. Yamaoka, P. C. Gaskell, et al.. (1998). Complete Genomic Screen in Late-Onset Familial Alzheimer’s Disease. Neurobiology of Aging. 19(1). S39–S42. 44 indexed citations
9.
Andersen, J. S., R. Rand Allingham, Einar Stefánsson, et al.. (1997). Genetic and clinical evaluation of pedigrees affected by pseudoexfoliation from Nova Scotia and Iceland. Investigative Ophthalmology & Visual Science. 38(4). 3 indexed citations
10.
Paz, Monica A. De La, Margaret A. Pericak‐Vance, Felicia Lennon, J. L. Haines, & Johanna M. Seddon. (1997). Exclusion of TIMP3 as a candidate locus in age-related macular degeneration.. PubMed. 38(6). 1060–5. 77 indexed citations
11.
Kwiatkowska, J., Elizabeth P. Henske, J. L. Haines, et al.. (1997). Cloning and evaluation of RALGDS as a candidate for the tuberous sclerosis gene TSC1. Annals of Human Genetics. 61(4). 299–305. 6 indexed citations
12.
Allingham, R. Rand, Janey L. Wiggs, K. F. Damji, et al.. (1996). Genes linked to systemic hypertension (HTN) and Maturity Onset Diabetes of the Young (MODY) are not associated with Primary Open Angle Glaucoma (POAG). Investigative Ophthalmology & Visual Science. 37(3). 1 indexed citations
13.
Figlewicz, Denise A., Melvin G. McInnis, Jun Goto, et al.. (1994). Identification of flanking markers for the familial amyotrophic lateral sclerosis gene ALS1 on chromosome 21. Journal of the Neurological Sciences. 124. 90–95. 6 indexed citations
14.
Yan, Wei, Terry J. Lerner, J. L. Haines, & James F. Gusella. (1994). Sequence Analysis and Mapping of a Novel Human Mitochondrial ATP Synthase Subunit 9 cDNA (ATP5G3). Genomics. 24(2). 375–377. 42 indexed citations
15.
Blumenfeld, Anat, Susan Slaugenhaupt, Diane Lucente, et al.. (1993). The gene for familial dysautonomia is linked to chromosome 9 and shows strong linkage disequilibrium with D9S58. The Society for Neuroscience Abstracts. 19. 1463. 7 indexed citations
16.
Pericak‐Vance, Margaret A., Peter St George‐Hyslop, P. C. Gaskell, et al.. (1993). Linkage analysis in familial Alzheimer disease: Description of the Duke and Boston data sets. Genetic Epidemiology. 10(6). 361–364. 5 indexed citations
17.
Haines, J. L.. (1992). Chromlook: An interactive program for error detection and mapping in reference linkage data. Genomics. 14(2). 517–519. 14 indexed citations
18.
Povey, Sue, Mari‐Wyn Burley, M. Smith, et al.. (1991). An Attempt to Map Two Genes for Tuberous Sclerosis Using Novel Two‐Point Methodsa. Annals of the New York Academy of Sciences. 615(1). 298–305. 16 indexed citations
19.
Siakotos, A. N., J. L. Haines, & Glyn Dawson. (1991). Third International Symposium on the Neuronal Ceroid-Lipofuscinoses (Batten's Disease), Indianapolis, Indiana, USA. Journal of Medical Genetics. 28(4). 284–285. 1 indexed citations
20.
Smith, Moyra, Susan L. Smalley, Massimo Pandolfo, et al.. (1990). Mapping of a gene determining tuberous sclerosis to human chromosome 11q1411q23. Genomics. 6(1). 105–114. 83 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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