Eli Hatchwell

6.9k total citations
52 papers, 2.1k citations indexed

About

Eli Hatchwell is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Eli Hatchwell has authored 52 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Genetics, 26 papers in Molecular Biology and 13 papers in Cognitive Neuroscience. Recurrent topics in Eli Hatchwell's work include Genomic variations and chromosomal abnormalities (13 papers), Autism Spectrum Disorder Research (12 papers) and Genetics and Neurodevelopmental Disorders (10 papers). Eli Hatchwell is often cited by papers focused on Genomic variations and chromosomal abnormalities (13 papers), Autism Spectrum Disorder Research (12 papers) and Genetics and Neurodevelopmental Disorders (10 papers). Eli Hatchwell collaborates with scholars based in United States, United Kingdom and Canada. Eli Hatchwell's co-authors include Jasmin Roohi, John M. Greally, Carla J. DeVincent, Kenneth D. Gadow, John A. Crolla, Todd Richmond, María E. Figueroa, Roland D. Green, Ari Melnick and Reid F. Thompson and has published in prestigious journals such as Nucleic Acids Research, Journal of the American College of Cardiology and Chemical Communications.

In The Last Decade

Eli Hatchwell

52 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eli Hatchwell United States 24 1.2k 984 534 172 142 52 2.1k
Jonathan Picker United States 24 1.0k 0.9× 1.3k 1.3× 670 1.3× 145 0.8× 251 1.8× 47 2.1k
Brenda Finucane United States 26 1.2k 1.0× 1.8k 1.9× 921 1.7× 110 0.6× 163 1.1× 65 2.6k
Bridget A. Fernandez Canada 22 1.1k 1.0× 1.5k 1.6× 752 1.4× 123 0.7× 396 2.8× 40 2.9k
Petter Strømme Norway 28 1.2k 1.0× 1.1k 1.2× 311 0.6× 243 1.4× 296 2.1× 76 2.7k
Kiran K. Mantripragada United Kingdom 22 773 0.7× 853 0.9× 274 0.5× 241 1.4× 100 0.7× 41 1.8k
Edmund C. Jenkins United States 31 1.1k 1.0× 1.7k 1.7× 822 1.5× 231 1.3× 334 2.4× 123 2.9k
Bronwyn Kerr United Kingdom 32 1.6k 1.4× 1.3k 1.3× 436 0.8× 127 0.7× 399 2.8× 67 3.2k
Tiziano Pramparo United States 27 1.7k 1.4× 1.2k 1.3× 503 0.9× 84 0.5× 219 1.5× 50 2.7k
Jeannie Visootsak United States 26 1.2k 1.1× 2.0k 2.0× 1.1k 2.1× 173 1.0× 298 2.1× 54 2.7k
Ragnheiður Fossdal Iceland 15 987 0.8× 1.5k 1.5× 580 1.1× 217 1.3× 211 1.5× 21 2.2k

Countries citing papers authored by Eli Hatchwell

Since Specialization
Citations

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

Fields of papers citing papers by Eli Hatchwell

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eli Hatchwell

This figure shows the co-authorship network connecting the top 25 collaborators of Eli Hatchwell. A scholar is included among the top collaborators of Eli Hatchwell 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 Eli Hatchwell. Eli Hatchwell 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.
Bronson, Richard, et al.. (2017). Detection of candidate nectin gene mutations in infertile men with severe teratospermia. Journal of Assisted Reproduction and Genetics. 34(10). 1295–1302. 4 indexed citations
2.
Gadow, Kenneth D., et al.. (2012). Allele-specific associations of 5-HTTLPR/rs25531 with ADHD and autism spectrum disorder. Progress in Neuro-Psychopharmacology and Biological Psychiatry. 40. 292–297. 29 indexed citations
3.
4.
Gadow, Kenneth D., Carla J. DeVincent, Doreen M. Olvet, et al.. (2010). Parent–child DRD4 genotype as a potential biomarker for oppositional, anxiety, and repetitive behaviors in children with autism spectrum disorder. Progress in Neuro-Psychopharmacology and Biological Psychiatry. 34(7). 1208–1214. 11 indexed citations
5.
Kantarci, Sibel, Kate G. Ackerman, Meaghan Russell, et al.. (2010). Characterization of the chromosome 1q41q42.12 region, and the candidate gene DISP1, in patients with CDH. American Journal of Medical Genetics Part A. 152A(10). 2493–2504. 40 indexed citations
6.
Williams, Stephen R., Santhosh Girirajan, David Tegay, et al.. (2009). Array comparative genomic hybridisation of 52 subjects with a Smith–Magenis-like phenotype: identification of dosage sensitive loci also associated with schizophrenia, autism, and developmental delay. Journal of Medical Genetics. 47(4). 223–229. 19 indexed citations
7.
Williams, Stephen R., Sureni V. Mullegama, Jill A. Rosenfeld, et al.. (2009). Haploinsufficiency of MBD5 associated with a syndrome involving microcephaly, intellectual disabilities, severe speech impairment, and seizures. European Journal of Human Genetics. 18(4). 436–441. 61 indexed citations
8.
Hatchwell, Eli, et al.. (2009). Differential binding of Escherichia coli McrA protein to DNA sequences that contain the dinucleotide m5CpG. Nucleic Acids Research. 38(6). 1997–2005. 20 indexed citations
9.
Roohi, Jasmin, et al.. (2008). An improved method for generating BAC DNA suitable for FISH. Cytogenetic and Genome Research. 121(1). 7–9. 18 indexed citations
10.
Christian, Susan L., Camille W. Brune, Jyotsna Sudi, et al.. (2008). Novel Submicroscopic Chromosomal Abnormalities Detected in Autism Spectrum Disorder. Biological Psychiatry. 63(12). 1111–1117. 216 indexed citations
11.
Roohi, Jasmin, Carla J. DeVincent, Eli Hatchwell, & Kenneth D. Gadow. (2008). Association of a Monoamine Oxidase-A Gene Promoter Polymorphism With ADHD and Anxiety in Boys With Autism Spectrum Disorder. Journal of Autism and Developmental Disorders. 39(1). 67–74. 35 indexed citations
12.
Roohi, Jasmin, David Tegay, John Pomeroy, et al.. (2008). A de novo apparently balanced translocation [46,XY,t(2;9)(p13;p24)] interrupting RAB11FIP5 identifies a potential candidate gene for autism spectrum disorder. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 147B(4). 411–417. 14 indexed citations
13.
Pernodet, Nadine, et al.. (2007). Multicomponent polymer coating to block photocatalytic activity of TiO2 nanoparticles. Chemical Communications. 4815–4815. 40 indexed citations
14.
Tegay, David, Andrew Lane, Jasmin Roohi, & Eli Hatchwell. (2007). Contiguous gene deletion involving L1CAM and AVPR2 causes X‐linked hydrocephalus with nephrogenic diabetes insipidus. American Journal of Medical Genetics Part A. 143A(6). 594–598. 18 indexed citations
15.
Khulan, Batbayar, Reid F. Thompson, Kenny Ye, et al.. (2006). Comparative isoschizomer profiling of cytosine methylation: The HELP assay. Genome Research. 16(8). 1046–1055. 287 indexed citations
16.
Herbert, Martha R., John Russo, San‐Duk Yang, et al.. (2006). Autism and environmental genomics. NeuroToxicology. 27(5). 671–684. 124 indexed citations
17.
Hatchwell, Eli, et al.. (1998). Molecular confirmation of germ line mosaicism for a submicroscopic deletion of chromosome 22q11. American Journal of Medical Genetics. 78(2). 103–106. 23 indexed citations
18.
Coppin, Brian, Isabella Moore, & Eli Hatchwell. (1997). Extending the overlap of three congenital overgrowth syndromes. Clinical Genetics. 51(6). 375–378. 17 indexed citations
19.
Webber, Steven A., Eli Hatchwell, John Barber, et al.. (1995). 762-4 Importance of Microdeletions of Chromosomal Region 22q11 In the Etiology of Congenital Conotruncal Malformations: A 2 Year Prospective Study. Journal of the American College of Cardiology. 25(2). 271A–271A. 1 indexed citations
20.

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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