K. Friend

1.3k total citations
8 papers, 773 citations indexed

About

K. Friend is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, K. Friend has authored 8 papers receiving a total of 773 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 4 papers in Cellular and Molecular Neuroscience and 3 papers in Genetics. Recurrent topics in K. Friend's work include Genetic Neurodegenerative Diseases (4 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Mitochondrial Function and Pathology (2 papers). K. Friend is often cited by papers focused on Genetic Neurodegenerative Diseases (4 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Mitochondrial Function and Pathology (2 papers). K. Friend collaborates with scholars based in Australia, United Kingdom and Slovakia. K. Friend's co-authors include Robert I. Richards, Julie Evans, Carolyn Ellaway, Catherine M. Watson, Linda S. Weaving, Hayley Archer, Bruce Bennetts, Helen Leonard, Hooshang Lahooti and Sarah Williamson and has published in prestigious journals such as Nature Genetics, Neurology and The American Journal of Human Genetics.

In The Last Decade

K. Friend

8 papers receiving 751 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
K. Friend Australia	7	523	482	209	145	63	8	773
Roberta Polli Italy	15	508 1.0×	470 1.0×	47 0.2×	204 1.4×	85 1.3×	32	868
Maria Teresa Bonati Italy	14	330 0.6×	327 0.7×	73 0.3×	208 1.4×	97 1.5×	44	756
Elizabeth Zuniga United States	5	276 0.5×	372 0.8×	98 0.5×	105 0.7×	28 0.4×	5	696
Guohe Tan China	9	331 0.6×	270 0.6×	140 0.7×	72 0.5×	188 3.0×	22	659
Stefania Bigoni Italy	14	255 0.5×	190 0.4×	105 0.5×	90 0.6×	82 1.3×	33	520
Jordi Guimerá Spain	13	293 0.6×	561 1.2×	182 0.9×	54 0.4×	13 0.2×	18	861
Claude Cancès France	10	310 0.6×	293 0.6×	66 0.3×	89 0.6×	115 1.8×	15	574
Hayley Archer United Kingdom	14	1.0k 2.0×	558 1.2×	69 0.3×	407 2.8×	133 2.1×	17	1.1k
Shino Shimada Japan	15	318 0.6×	315 0.7×	68 0.3×	35 0.2×	43 0.7×	36	545
Gilda Stefanelli Canada	12	441 0.8×	551 1.1×	97 0.5×	155 1.1×	12 0.2×	19	734

Countries citing papers authored by K. Friend

Since Specialization

Citations

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

Fields of papers citing papers by K. Friend

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of K. Friend

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

All Works

Sort: Min cites: Since: Top N: Style:

8 of 8 papers shown

1.

Huang, Lijia, Jodi Warman‐Chardon, Melissa T. Carter, et al.. (2012). Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia. Orphanet Journal of Rare Diseases. 7(1). 67–67. 104 indexed citations

2.

Yu, Shuancang, Kathleen H. Cox, K. Friend, et al.. (2007). Familial 22q11.2 duplication: a three‐generation family with a 3‐Mb duplication and a familial 1.5‐Mb duplication. Clinical Genetics. 73(2). 160–164. 46 indexed citations

3.

Weaving, Linda S., John Christodoulou, Sarah Williamson, et al.. (2004). Mutations of CDKL5 Cause a Severe Neurodevelopmental Disorder with Infantile Spasms and Mental Retardation. The American Journal of Human Genetics. 75(6). 1079–1093. 375 indexed citations

4.

Dudding, Tracy, et al.. (2004). Autosomal dominant congenital non-progressive ataxia overlaps with the SCA15 locus. Neurology. 63(12). 2288–2292. 58 indexed citations

5.

Benson, Kathleen F., Marshall S. Horwitz, John Wolff, et al.. (1998). CAG Repeat Expansion in Autosomal Dominant Familial Spastic Paraparesis: Novel Expansion in a Subset of Patients. Human Molecular Genetics. 7(11). 1779–1786. 20 indexed citations

6.

Richards, Robert I., Joanna Crawford, Kouji Narahara, et al.. (1996). Dynamic mutation loci: allele distributions in different populations. Annals of Human Genetics. 60(5). 391–400. 17 indexed citations

7.

Richards, Robert I., K. Holman, K. Friend, et al.. (1994). FRAXAC2 instability. Nature Genetics. 7(2). 122–122. 1 indexed citations

8.

Richards, Robert I., Katherine Holman, K. Friend, et al.. (1992). Evidence of founder chromosomes in fragile X syndrome. Nature Genetics. 1(4). 257–260. 152 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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