Jennifer Chellis

545 total citations
5 papers, 216 citations indexed

About

Jennifer Chellis is a scholar working on Genetics, Experimental and Cognitive Psychology and Clinical Psychology. According to data from OpenAlex, Jennifer Chellis has authored 5 papers receiving a total of 216 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 2 papers in Experimental and Cognitive Psychology and 1 paper in Clinical Psychology. Recurrent topics in Jennifer Chellis's work include Genetics and Neurodevelopmental Disorders (5 papers), Genetic Associations and Epidemiology (3 papers) and Genetic Syndromes and Imprinting (2 papers). Jennifer Chellis is often cited by papers focused on Genetics and Neurodevelopmental Disorders (5 papers), Genetic Associations and Epidemiology (3 papers) and Genetic Syndromes and Imprinting (2 papers). Jennifer Chellis collaborates with scholars based in United States and United Kingdom. Jennifer Chellis's co-authors include J. Raymond DePaulo, Dean F. MacKinnon, Melvin G. McInnis, Myrna M. Weissman, Kathleen P. Murphy-Eberenz, James A. Knowles, Wendy N. Zubenko, J. Regan Thomas, Raymond R. Crowe and Philip Adams and has published in prestigious journals such as The American Journal of Human Genetics and American Journal of Medical Genetics Part B Neuropsychiatric Genetics.

In The Last Decade

Jennifer Chellis

5 papers receiving 211 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jennifer Chellis United States	4	114	67	46	39	39	5	216
Julia Perry United Kingdom	7	85 0.7×	81 1.2×	40 0.9×	71 1.8×	42 1.1×	9	266
Alex Hatzimanolis Greece	10	127 1.1×	111 1.7×	46 1.0×	43 1.1×	42 1.1×	14	280
Charlotte Dennison United Kingdom	7	97 0.9×	104 1.6×	35 0.8×	41 1.1×	47 1.2×	18	232
Maria Tropeano United Kingdom	11	150 1.3×	55 0.8×	96 2.1×	98 2.5×	62 1.6×	13	372
Douglas F. Levinson United States	11	172 1.5×	108 1.6×	105 2.3×	59 1.5×	40 1.0×	16	328
Melvin Mclnnis United States	3	133 1.2×	140 2.1×	61 1.3×	65 1.7×	24 0.6×	4	302
N. Mori Japan	10	36 0.3×	69 1.0×	47 1.0×	63 1.6×	46 1.2×	14	254
C. A. Kaufmann United States	6	98 0.9×	144 2.1×	50 1.1×	58 1.5×	22 0.6×	11	298
Daniël Roelfs Norway	8	74 0.6×	39 0.6×	38 0.8×	17 0.4×	79 2.0×	14	230

Countries citing papers authored by Jennifer Chellis

Since Specialization

Citations

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

Fields of papers citing papers by Jennifer Chellis

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jennifer Chellis

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

All Works

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5 of 5 papers shown

Holmans, Peter, George S. Zubenko, Raymond R. Crowe, et al.. (2004). Genomewide Significant Linkage to Recurrent, Early-Onset Major Depressive Disorder on Chromosome 15q. The American Journal of Human Genetics. 74(6). 1154–1167. 87 indexed citations

Zandi, Peter P., Virginia L. Willour, Jennifer Chellis, et al.. (2003). Genome scan of a second wave of NIMH genetics initiative bipolar pedigrees: chromosomes 2, 11, 13, 14, and X. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 119B(1). 69–76. 35 indexed citations

Willour, Virginia L., Peter P. Zandi, Yuqing Huo, et al.. (2003). Genome scan of the fifty‐six bipolar pedigrees from the NIMH genetics initiative replication sample: Chromosomes 4, 7, 9, 18, 19, 20, and 21. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 121B(1). 21–27. 30 indexed citations

Levinson, Douglas F., George S. Zubenko, Raymond R. Crowe, et al.. (2003). Genetics of recurrent early‐onset depression (GenRED): Design and preliminary clinical characteristics of a repository sample for genetic linkage studies. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 119B(1). 118–130. 63 indexed citations

Willour, Virginia L., Peter P. Zandi, Yuqing Huo, et al.. (2003). Rapid Publication Genome Scan of the Fifty-Six Bipolar Pedigrees From the NIMH Genetics Initiative Replication Sample: Chromosomes 4, 7, 9, 18, 19, 20, and 21. 1 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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