Elli Kempas

968 total citations
11 papers, 706 citations indexed

About

Elli Kempas is a scholar working on Cognitive Neuroscience, Genetics and Epidemiology. According to data from OpenAlex, Elli Kempas has authored 11 papers receiving a total of 706 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Cognitive Neuroscience, 10 papers in Genetics and 3 papers in Epidemiology. Recurrent topics in Elli Kempas's work include Autism Spectrum Disorder Research (10 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Genomic variations and chromosomal abnormalities (4 papers). Elli Kempas is often cited by papers focused on Autism Spectrum Disorder Research (10 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Genomic variations and chromosomal abnormalities (4 papers). Elli Kempas collaborates with scholars based in Finland, United States and United Kingdom. Elli Kempas's co-authors include Tero Ylisaukko‐oja, Irma Järvelä, Leena Peltonen, Raija Vanhala, Mari Auranen, Teppo Varilo, Kristin L. Ayers, Lennart von Wendt, Karola Rehnström and Janet S. Sinsheimer and has published in prestigious journals such as Annals of Neurology, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Elli Kempas

11 papers receiving 667 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Elli Kempas Finland	10	477	384	242	64	59	11	706
Barbara Manzi Italy	13	516 1.1×	633 1.6×	284 1.2×	57 0.9×	35 0.6×	17	979
S. L. Donnelly United States	7	549 1.2×	543 1.4×	229 0.9×	32 0.5×	12 0.2×	9	793
Elena Bacchelli Italy	16	512 1.1×	383 1.0×	343 1.4×	96 1.5×	20 0.3×	28	791
Meredyth P. Bass United States	14	779 1.6×	475 1.2×	350 1.4×	73 1.1×	24 0.4×	17	1.1k
Robert DeLong United States	9	337 0.7×	370 1.0×	191 0.8×	111 1.7×	15 0.3×	12	709
Karola Rehnström Finland	14	432 0.9×	256 0.7×	257 1.1×	58 0.9×	9 0.2×	21	760
Daniel Moreno‐De‐Luca United States	9	413 0.9×	389 1.0×	179 0.7×	26 0.4×	20 0.3×	16	677
Assunção Ataíde Portugal	8	433 0.9×	501 1.3×	196 0.8×	55 0.9×	29 0.5×	8	691
Irina Zaharieva United Kingdom	13	495 1.0×	261 0.7×	536 2.2×	97 1.5×	10 0.2×	20	1.1k
Simone Berkel Germany	11	461 1.0×	342 0.9×	376 1.6×	157 2.5×	37 0.6×	13	747

Countries citing papers authored by Elli Kempas

Since Specialization

Citations

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

Fields of papers citing papers by Elli Kempas

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elli Kempas

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

All Works

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11 of 11 papers shown

Kilpinen, Helena, Tero Ylisaukko‐oja, Karola Rehnström, et al.. (2009). Linkage and linkage disequilibrium scan for autism loci in an extended pedigree from Finland. Human Molecular Genetics. 18(15). 2912–2921. 22 indexed citations

Rehnström, Karola, Tero Ylisaukko‐oja, Pekka Ellonen, et al.. (2008). Allelic variants in HTR3C show association with autism. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 150B(5). 741–746. 14 indexed citations

Turunen, Joni A., Karola Rehnström, Helena Kilpinen, et al.. (2008). Mitochondrial aspartate/glutamate carrier SLC25A12 gene is associated with autism. Autism Research. 1(3). 189–192. 36 indexed citations

Turunen, Joni A., Tero Ylisaukko‐oja, Helena Kilpinen, et al.. (2006). Association analysis of SLC25A12 and EN2 in the Finnish families with autism-spectrum disorders. 766–766. 3 indexed citations

Ylisaukko‐oja, Tero, Karola Rehnström, Mari Auranen, et al.. (2005). Analysis of four neuroligin genes as candidates for autism. European Journal of Human Genetics. 13(12). 1285–1292. 114 indexed citations

Ylisaukko‐oja, Tero, Maricela Alarcón, Rita M. Cantor, et al.. (2005). Search for autism loci by combined analysis of Autism Genetic Resource Exchange and Finnish families. Annals of Neurology. 59(1). 145–155. 100 indexed citations

Ylisaukko‐oja, Tero, Taina Nieminen‐von Wendt, Elli Kempas, et al.. (2004). Genome-wide scan for loci of Asperger syndrome. Molecular Psychiatry. 9(2). 161–168. 60 indexed citations

Ylisaukko‐oja, Tero, Karola Rehnström, Raija Vanhala, et al.. (2004). MECP2 mutation analysis in patients with mental retardation. American Journal of Medical Genetics Part A. 132A(2). 121–124. 24 indexed citations

Auranen, Mari, Teppo Varilo, Reija Alén, et al.. (2003). Evidence for allelic association on chromosome 3q25–27 in families with autism spectrum disorders originating from a subisolate of Finland. Molecular Psychiatry. 8(10). 879–884. 29 indexed citations

10.

Auranen, Mari, Raija Vanhala, Teppo Varilo, et al.. (2002). A Genomewide Screen for Autism-Spectrum Disorders: Evidence for a Major Susceptibility Locus on Chromosome 3q25-27. The American Journal of Human Genetics. 71(4). 777–790. 174 indexed citations

11.

Pajukanta, Päivi, Michele Cargill, Laura Viitanen, et al.. (2000). Two Loci on Chromosomes 2 and X for Premature Coronary Heart Disease Identified in Early- and Late-Settlement Populations of Finland. The American Journal of Human Genetics. 67(6). 1481–1493. 130 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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