James Jaworski

1.9k total citations
19 papers, 951 citations indexed

About

James Jaworski is a scholar working on Genetics, Cognitive Neuroscience and Molecular Biology. According to data from OpenAlex, James Jaworski has authored 19 papers receiving a total of 951 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 16 papers in Cognitive Neuroscience and 7 papers in Molecular Biology. Recurrent topics in James Jaworski's work include Autism Spectrum Disorder Research (16 papers), Genomic variations and chromosomal abnormalities (14 papers) and Genetics and Neurodevelopmental Disorders (13 papers). James Jaworski is often cited by papers focused on Autism Spectrum Disorder Research (16 papers), Genomic variations and chromosomal abnormalities (14 papers) and Genetics and Neurodevelopmental Disorders (13 papers). James Jaworski collaborates with scholars based in United States, Spain and Norway. James Jaworski's co-authors include Michael L. Cuccaro, John R. Gilbert, Eden R. Martin, Ioanna Konidari, Jonathan L. Haines, Patrice L. Whitehead, Ruth K. Abramson, Margaret A. Pericak‐Vance, Deqiong Ma and Margaret A. Pericak‐Vance and has published in prestigious journals such as PLoS ONE, American Journal of Psychiatry and Human Molecular Genetics.

In The Last Decade

James Jaworski

19 papers receiving 929 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
James Jaworski United States	17	588	546	372	153	75	19	951
Virpi Leppä United States	9	542 0.9×	421 0.8×	645 1.7×	88 0.6×	47 0.6×	11	1.1k
Holly N. Cukier United States	16	518 0.9×	403 0.7×	525 1.4×	147 1.0×	46 0.6×	26	1.0k
SakkuBai Naidu United States	15	643 1.1×	354 0.6×	483 1.3×	87 0.6×	66 0.9×	18	991
Haley E. Speed United States	13	484 0.8×	466 0.9×	357 1.0×	265 1.7×	85 1.1×	16	884
Vijayendran Chandran United States	11	542 0.9×	379 0.7×	709 1.9×	169 1.1×	75 1.0×	16	1.1k
Claudio Toma Spain	21	527 0.9×	359 0.7×	359 1.0×	153 1.0×	29 0.4×	41	1.0k
Yujun Shao United States	9	736 1.3×	739 1.4×	313 0.8×	93 0.6×	64 0.9×	18	1.0k
Amanda L. Yonan United States	7	458 0.8×	482 0.9×	332 0.9×	186 1.2×	33 0.4×	7	904
Ismail Thanseem Japan	15	317 0.5×	262 0.5×	462 1.2×	98 0.6×	57 0.8×	28	877
Janet Berrios United States	6	443 0.8×	393 0.7×	394 1.1×	190 1.2×	59 0.8×	8	922

Countries citing papers authored by James Jaworski

Since Specialization

Citations

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

Fields of papers citing papers by James Jaworski

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of James Jaworski

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

All Works

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19 of 19 papers shown

Cukier, Holly N., Karyn L. Hamilton, Patrice L. Whitehead, et al.. (2017). Exome Sequencing of Extended Families with Alzheimer’s Disease Identifies Novel Genes Implicated in Cell Immunity and Neuronal Function. Journal of Alzheimer’s Disease & Parkinsonism. 7(4). 20 indexed citations

Griswold, Anthony J., Nicole Dueker, Derek Van Booven, et al.. (2015). Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variants. Molecular Autism. 6(1). 43–43. 46 indexed citations

Hedges, Dale J., Kara L. Hamilton‐Nelson, Stephanie Sacharow, et al.. (2012). Evidence of novel fine-scale structural variation at autism spectrum disorder candidate loci. Molecular Autism. 3(1). 2–2. 29 indexed citations

Griswold, Anthony J., Deqiong Ma, Holly N. Cukier, et al.. (2012). Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways. Human Molecular Genetics. 21(15). 3513–3523. 143 indexed citations

Hussman, John P., Ren-Hua Chung, Anthony J. Griswold, et al.. (2011). A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism. Molecular Autism. 2(1). 1–1. 171 indexed citations

Griswold, Anthony J., Deqiong Ma, Stephanie Sacharow, et al.. (2011). A de novo 1.5 Mb microdeletion on chromosome 14q23.2‐23.3 in a patient with autism and spherocytosis. Autism Research. 4(3). 221–227. 24 indexed citations

Salyakina, Daria, Holly N. Cukier, Joycelyn M. Lee, et al.. (2011). Copy Number Variants in Extended Autism Spectrum Disorder Families Reveal Candidates Potentially Involved in Autism Risk. PLoS ONE. 6(10). e26049–e26049. 57 indexed citations

Chung, Ren-Hua, Deqiong Ma, Kai Wang, et al.. (2011). An X chromosome-wide association study in autism families identifies TBL1X as a novel autism spectrum disorder candidate gene in males. Molecular Autism. 2(1). 18–18. 31 indexed citations

Salyakina, Daria, James Jaworski, Ioanna Konidari, et al.. (2010). Variants in several genomic regions associated with asperger disorder. Autism Research. 3(6). 303–310. 25 indexed citations

10.

Rabionet, Raquel, Ioanna Konidari, James Jaworski, et al.. (2009). Association and gene–gene interaction of SLC6A4 and ITGB3 in autism. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 153B(2). 477–483. 40 indexed citations

11.

Cukier, Holly N., David Skaar, Ioanna Konidari, et al.. (2009). Identification of chromosome 7 inversion breakpoints in an autistic family narrows candidate region for autism susceptibility. Autism Research. 2(5). 258–266. 11 indexed citations

12.

Ashley‐Koch, Allison E., James Jaworski, Hao Mei, et al.. (2007). Investigation of potential gene–gene interactions between apoe and reln contributing to autism risk. Psychiatric Genetics. 17(4). 221–226. 33 indexed citations

13.

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

14.

Ashley‐Koch, Allison E., Hao Mei, James Jaworski, et al.. (2006). An Analysis Paradigm for Investigating Multi‐locus Effects in Complex Disease: Examination of Three GABA_A Receptor Subunit Genes on 15q11‐q13 as Risk Factors for Autistic Disorder.. Annals of Human Genetics. 70(3). 281–292. 46 indexed citations

15.

Rabionet, Raquel, Jacob L. McCauley, James Jaworski, et al.. (2006). Lack of Association Between Autism and SLC25A12. American Journal of Psychiatry. 163(5). 929–931. 32 indexed citations

16.

Jaworski, James, Marisa M. Menold, S. L. Donnelly, et al.. (2005). Ordered‐subset analysis of savant skills in autism for 15q11‐q13. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 135B(1). 38–41. 20 indexed citations

17.

Rabionet, Raquel, James Jaworski, Allison E. Ashley‐Koch, et al.. (2004). Analysis of the autism chromosome 2 linkage region: GAD1 and other candidate genes. Neuroscience Letters. 372(3). 209–214. 31 indexed citations

18.

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

19.

Ladd, Daniel, et al.. (2000). Transgenic mice with a mutated collagen promoter display normal response during bleomycin-induced fibrosis and possess neurological abnormalities. Journal of Cellular Biochemistry. 77(1). 135–148. 10 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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