K Stephens

494 total citations
133 papers, 296 citations indexed

About

K Stephens is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, K Stephens has authored 133 papers receiving a total of 296 indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Molecular Biology, 23 papers in Genetics and 14 papers in Cellular and Molecular Neuroscience. Recurrent topics in K Stephens's work include Metabolism and Genetic Disorders (13 papers), Neurogenetic and Muscular Disorders Research (10 papers) and Hereditary Neurological Disorders (7 papers). K Stephens is often cited by papers focused on Metabolism and Genetic Disorders (13 papers), Neurogenetic and Muscular Disorders Research (10 papers) and Hereditary Neurological Disorders (7 papers). K Stephens collaborates with scholars based in United States and United Kingdom. K Stephens's co-authors include Pagon Ra, Bean Ljh, Adam Mp, A Amemiya, Ardinger Hh, Mefford Hc, Bird Td, Smith Rjh, Fong Ct and Susan M. Abdel‐Rahman and has published in prestigious journals such as PLoS ONE, PEDIATRICS and Obesity.

In The Last Decade

K Stephens

112 papers receiving 288 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
K Stephens United States	7	79	52	43	39	37	133	296
Sayaka Ogawa Japan	10	73 0.9×	28 0.5×	21 0.5×	21 0.5×	50 1.4×	34	341
Carla Maria Ramos Germano Brazil	13	165 2.1×	162 3.1×	46 1.1×	34 0.9×	74 2.0×	53	679
Leanne Wallace Australia	13	118 1.5×	130 2.5×	61 1.4×	47 1.2×	40 1.1×	21	591
Shao‐Yin Chu Taiwan	13	128 1.6×	119 2.3×	73 1.7×	9 0.2×	79 2.1×	52	491
Fahad A. Bashiri Saudi Arabia	12	131 1.7×	96 1.8×	48 1.1×	11 0.3×	38 1.0×	63	552
Mingji Yi China	12	86 1.1×	42 0.8×	18 0.4×	22 0.6×	59 1.6×	42	443
MB Delatycki Australia	10	37 0.5×	89 1.7×	23 0.5×	96 2.5×	70 1.9×	12	377
Lindsay Fernández‐Rhodes United States	13	266 3.4×	150 2.9×	78 1.8×	14 0.4×	45 1.2×	37	678
Pernilla Stridh Sweden	14	146 1.8×	57 1.1×	27 0.6×	5 0.1×	28 0.8×	40	694
Katrina Evers Switzerland	9	94 1.2×	33 0.6×	31 0.7×	39 1.0×	6 0.2×	16	335

Countries citing papers authored by K Stephens

Since Specialization

Citations

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

Fields of papers citing papers by K Stephens

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of K Stephens

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

All Works

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20 of 20 papers shown

1.

Mp, Adam, Ardinger Hh, Pagon Ra, et al.. (2020). PAX6-Related Aniridia -- GeneReviews®. 1 indexed citations

2.

Mp, Adam, Ardinger Hh, Pagon Ra, et al.. (2019). FARS2 Deficiency -- GeneReviews®. 1 indexed citations

3.

Mp, Adam, Ardinger Hh, Pagon Ra, et al.. (2019). MBD5 Haploinsufficiency -- GeneReviews®. 1 indexed citations

4.

Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). ADAMTSL4-Related Eye Disorders -- GeneReviews®. 23(3).

5.

Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Neurofibromatosis 2 -- GeneReviews®. PLoS ONE. 13(12). e0208961–e0208961.

6.

Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). 15q24 Microdeletion Syndrome -- GeneReviews(®). 1 indexed citations

7.

Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Gaucher Disease -- GeneReviews(®). 4 indexed citations

8.

Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Rothmund-Thomson Syndrome -- GeneReviews®. 1 indexed citations

9.

Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). MED12-Related Disorders -- GeneReviews®.

10.

Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Polymicrogyria Overview -- GeneReviews®. 1 indexed citations

11.

Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Spinal Muscular Atrophy, X-Linked Infantile -- GeneReviews(®). 1 indexed citations

12.

Mp, Adam, Ardinger Hh, Pagon Ra, et al.. (2016). FMR1-Related Disorders -- GeneReviews(®). 1 indexed citations

13.

Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). TSEN54-Related Pontocerebellar Hypoplasia -- GeneReviews(®). 1 indexed citations

14.

Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Diamond-Blackfan Anemia -- GeneReviews®. 3 indexed citations

15.

Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Prader-Willi Syndrome -- GeneReviews®. 4 indexed citations

16.

Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Pachyonychia Congenita -- GeneReviews(®).

17.

Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). PLA2G6-Associated Neurodegeneration -- GeneReviews(®). 2 indexed citations

18.

Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Neurofibromatosis 1 -- GeneReviews(®). 6 indexed citations

19.

Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2015). Oculopharyngeal Muscular Dystrophy -- GeneReviews®. 2 indexed citations

20.

Stephens, K, et al.. (1989). Center Your Reading Instruction.. Instructor. 98(9). 42–45. 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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