J.L. Haines

2.1k total citations
20 papers, 853 citations indexed

About

J.L. Haines is a scholar working on Genetics, Cognitive Neuroscience and Molecular Biology. According to data from OpenAlex, J.L. Haines has authored 20 papers receiving a total of 853 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 5 papers in Cognitive Neuroscience and 4 papers in Molecular Biology. Recurrent topics in J.L. Haines's work include Genetics and Neurodevelopmental Disorders (8 papers), Autism Spectrum Disorder Research (5 papers) and Multiple Sclerosis Research Studies (4 papers). J.L. Haines is often cited by papers focused on Genetics and Neurodevelopmental Disorders (8 papers), Autism Spectrum Disorder Research (5 papers) and Multiple Sclerosis Research Studies (4 papers). J.L. Haines collaborates with scholars based in United States, Saudi Arabia and Canada. J.L. Haines's co-authors include Jacob L. McCauley, Susan E. Folstein, James S. Sutcliffe, Margaret A. Pericak‐Vance, John R. Gilbert, Rebecca L. Zuvich, James Jaworski, Margaret A. Pericak‐Vance, Michael L. Cuccaro and Tarek Tawfik Amin and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Neurology and Clinical Infectious Diseases.

In The Last Decade

J.L. Haines

20 papers receiving 824 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 15 319 300 247 120 112 20 853
Rezvan Noroozi Iran 21 257 0.8× 187 0.6× 654 2.6× 74 0.6× 118 1.1× 77 1.3k
Elisabetta Bolognesi Italy 21 207 0.6× 202 0.7× 257 1.0× 72 0.6× 228 2.0× 50 973
John P. Hussman United States 11 400 1.3× 473 1.6× 309 1.3× 165 1.4× 47 0.4× 14 964
Josette Mancini France 19 454 1.4× 305 1.0× 484 2.0× 90 0.8× 61 0.5× 29 1.2k
Valgerður Steinthórsdóttir Iceland 15 424 1.3× 85 0.3× 471 1.9× 182 1.5× 203 1.8× 26 1.6k
Annika Lekman Sweden 17 145 0.5× 105 0.3× 320 1.3× 229 1.9× 78 0.7× 25 848
Sarah H. Shaw United States 15 973 3.1× 153 0.5× 502 2.0× 131 1.1× 293 2.6× 20 1.6k
Abdul Noor Canada 20 620 1.9× 145 0.5× 823 3.3× 85 0.7× 51 0.5× 42 1.4k
Milena Zanzottera Italy 19 114 0.4× 141 0.5× 326 1.3× 60 0.5× 224 2.0× 49 1000
Ian Baker United Kingdom 11 140 0.4× 134 0.4× 252 1.0× 184 1.5× 33 0.3× 16 1.1k

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.
Reitz, Christiane, Giuseppe Tosto, Badri N. Vardarajan, et al.. (2013). Independent and epistatic effects of variants in VPS10-d receptors on Alzheimer disease risk and processing of the amyloid precursor protein (APP). Translational Psychiatry. 3(5). e256–e256. 58 indexed citations
2.
Schnetz‐Boutaud, Nathalie, Jonathan D. Bartlett, H Wright, et al.. (2009). Examination of association of genes in the serotonin system to autism. Neurogenetics. 10(3). 209–216. 55 indexed citations
3.
Zuvich, Rebecca L., Jacob L. McCauley, Margaret A. Pericak‐Vance, & J.L. Haines. (2009). Genetics and pathogenesis of multiple sclerosis. Seminars in Immunology. 21(6). 328–333. 66 indexed citations
4.
Barcellos, Lisa F., Patricia P. Ramsay, Stacy J. Caillier, et al.. (2008). Genetic variation in nitric oxide synthase 2A (NOS2A) and risk for multiple sclerosis. Genes and Immunity. 9(6). 493–500. 5 indexed citations
5.
Abou‐Khalil, Bassel, et al.. (2007). Familial genetic predisposition, epilepsy localization and antecedent febrile seizures. Epilepsy Research. 73(1). 104–110. 25 indexed citations
6.
Ritchie, Marylyn D., David W. Haas, Alison A. Motsinger‐Reif, et al.. (2006). Drug Transporter and Metabolizing Enzyme Gene Variants and Nonnucleoside Reverse-Transcriptase Inhibitor Hepatotoxicity. Clinical Infectious Diseases. 43(6). 779–782. 73 indexed citations
7.
Cuccaro, Michael L., James Jaworski, Carol Haynes, et al.. (2006). Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14. Molecular Psychiatry. 12(4). 376–384. 37 indexed citations
8.
Schmidt, Silke, Margaret A. Pericak‐Vance, Stephen Sawcer, et al.. (2006). Allelic association of sequence variants in the herpes virus entry mediator-B gene (PVRL2) with the severity of multiple sclerosis. Genes and Immunity. 7(5). 384–392. 13 indexed citations
9.
Brassat, David, Alison A. Motsinger‐Reif, Stacy J. Caillier, et al.. (2006). Multifactor dimensionality reduction reveals gene–gene interactions associated with multiple sclerosis susceptibility in African Americans. Genes and Immunity. 7(4). 310–315. 41 indexed citations
10.
Saeed, Mohammad, N. Siddique, Lisa Dellefave, et al.. (2006). Lack of association of VEGF promoter polymorphisms with sporadic ALS. Neurology. 67(3). 508–510. 21 indexed citations
11.
Kallianpur, Asha, Lynn Hall, Meeta Yadav, et al.. (2005). The hemochromatosis C282Y allele: a risk factor for hepatic veno-occlusive disease after hematopoietic stem cell transplantation. Bone Marrow Transplantation. 35(12). 1155–1164. 28 indexed citations
12.
Schmidt, Stefanie J., Eric A. Postel, Anita Agarwal, et al.. (2004). Analysis of nitric oxide synthase genes in age–related macular degeneration. Investigative Ophthalmology & Visual Science. 45(13). 2719–2719. 1 indexed citations
13.
Skaar, David, Yujun Shao, J.L. Haines, et al.. (2004). Analysis of the RELN gene as a genetic risk factor for autism. Molecular Psychiatry. 10(6). 563–571. 145 indexed citations
14.
Schmidt, Sabine, et al.. (2004). Cigarette smoking and APOE genotype interaction in age related macular degeneration. 45(13). 2302–2302. 2 indexed citations
15.
McCauley, Jacob L., Lana M. Olson, Michael Dowd, et al.. (2003). Linkage and association analysis at the serotonin transporter (SLC6A4) locus in a rigid‐compulsive subset of autism. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 127B(1). 104–112. 110 indexed citations
16.
Hutcheson, Holli B., Yvonne M. Bradford, Susan E. Folstein, et al.. (2002). Defining the autism minimum candidate gene region on chromosome 7. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 117B(1). 90–96. 31 indexed citations
17.
Haines, J.L. & Margaret A. Pericak‐Vance. (1999). Genetics of Multiple Sclerosis. PubMed. 1. 273–288. 6 indexed citations
18.
Ionâşescu, Victor, James A. Trofatter, J.L. Haines, R. Ionasescu, & Charles Searby. (1992). Mapping of the gene for X‐linked dominant Charcot‐Marie‐Tooth neuropathy. Neurology. 42(4). 903–903. 24 indexed citations
19.
Hayden, Michael R., Jeff Hewitt, John J. Wasmuth, et al.. (1988). A polymorphic DNA marker that represents a conserved expressed sequence in the region of the Huntington disease gene.. PubMed. 42(1). 125–31. 21 indexed citations
20.
Baehner, Robert L., Louis M. Kunkel, Anthony P. Monaco, et al.. (1986). DNA linkage analysis of X chromosome-linked chronic granulomatous disease.. Proceedings of the National Academy of Sciences. 83(10). 3398–3401. 91 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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