K. Fried

1.1k total citations
64 papers, 844 citations indexed

About

K. Fried is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, K. Fried has authored 64 papers receiving a total of 844 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Genetics, 17 papers in Molecular Biology and 13 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in K. Fried's work include Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (8 papers) and Genetics and Neurodevelopmental Disorders (6 papers). K. Fried is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (8 papers) and Genetics and Neurodevelopmental Disorders (6 papers). K. Fried collaborates with scholars based in Israel, United Kingdom and United States. K. Fried's co-authors include G Mundel, M Rosenblatt, Y Matoth, Alan E H Emery, S Kaufman, Esther Kahana, Amos D. Korczyn, Nelly Zilber, Milton Alter and R. Krikler and has published in prestigious journals such as The Lancet, Annals of the New York Academy of Sciences and Journal of Animal Science.

In The Last Decade

K. Fried

61 papers receiving 770 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
K. Fried Israel	16	337	301	149	127	117	64	844
L. A. Sandkuyl Netherlands	18	550 1.6×	297 1.0×	72 0.5×	182 1.4×	111 0.9×	29	1.1k
Juan Chemke Israel	20	365 1.1×	327 1.1×	220 1.5×	65 0.5×	152 1.3×	64	1.1k
Naomi Fitch Canada	22	479 1.4×	585 1.9×	186 1.2×	95 0.7×	262 2.2×	44	1.1k
Harold E. Cross United States	19	583 1.7×	363 1.2×	66 0.4×	44 0.3×	80 0.7×	43	1.3k
Oswaldo Frota‐Pessoa Brazil	14	290 0.9×	235 0.8×	55 0.4×	63 0.5×	58 0.5×	65	711
M D Crawfurd United Kingdom	18	250 0.7×	290 1.0×	129 0.9×	50 0.4×	80 0.7×	33	705
Diana García‐Cruz Mexico	16	272 0.8×	356 1.2×	112 0.8×	72 0.6×	131 1.1×	81	727
Ajit J. Alles United States	15	318 0.9×	88 0.3×	158 1.1×	123 1.0×	162 1.4×	18	852
J.W. Delleman Netherlands	17	360 1.1×	275 0.9×	89 0.6×	35 0.3×	84 0.7×	45	872
Tim Donlon United States	18	607 1.8×	672 2.2×	254 1.7×	53 0.4×	76 0.6×	26	1.3k

Countries citing papers authored by K. Fried

Since Specialization

Citations

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

Fields of papers citing papers by K. Fried

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

This figure shows the co-authorship network connecting the top 25 collaborators of K. Fried. A scholar is included among the top collaborators of K. Fried 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. Fried. K. Fried 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:

20 of 20 papers shown

Almoznino‐Sarafian, Dorit, Joshua Weissgarten, Irena Alon, et al.. (1997). Benign familial microcytic thrombocytosis with autosomal dominant transmission. Clinical Genetics. 52(1). 47–50. 9 indexed citations

Bistritzer, Tzvy, et al.. (1993). Congenital contractural arachnodactyly in two double second cousins: possible homozygosity. Clinical Genetics. 44(1). 15–19. 13 indexed citations

Zilber, Nelly, Amos D. Korczyn, Esther Kahana, K. Fried, & Milton Alter. (1984). Inheritance of idiopathic torsion dystonia among Jews.. Journal of Medical Genetics. 21(1). 13–20. 59 indexed citations

Fried, K., et al.. (1984). Genetic microcephaly in a pair of monozygous twins. Teratology. 29(2). 177–180. 2 indexed citations

Fried, K., et al.. (1981). Probable autosomal dominant infantile pyloric stenosis in a large kindred. Clinical Genetics. 20(5). 328–330. 20 indexed citations

Fried, K., et al.. (1981). Autosomal dominant inheritance with incomplete penetrance of Caffey disease (infantile cortical hyperostosis). Clinical Genetics. 19(4). 271–274. 9 indexed citations

Fried, K. & M Rosenblatt. (1979). A Familial Extra Small Marker Autosome in Persons with Normal Phenotype. Human Heredity. 29(6). 371–373. 4 indexed citations

Fried, K., et al.. (1979). Autosomal recessive sudden unexpected death in children probably caused by a cardiomyopathy associated with myopathy.. Journal of Medical Genetics. 16(5). 341–346. 1 indexed citations

Fried, K., et al.. (1978). Biochemical, genetic and ultrastructural study of a family with the sea‐blue histiocyte syndrome/chronic non‐neuronopathic Niemann‐ Pick disease. European Journal of Clinical Investigation. 8(4). 249–253. 8 indexed citations

10.

Fried, K., et al.. (1977). Familial Balanced Reciprocal Translocation t(1;16) (q12;p13) Ascertained because of Multiple Abortions in a Carrier. Human Heredity. 27(5). 362–365. 4 indexed citations

11.

Fried, K., et al.. (1977). Mental retardation with 45 chromosomes 45,XX,--5,--14,+der(5) t(5,14)(p15;q13) mat due to familial balanced reciprocal translocation.. Journal of Medical Genetics. 14(1). 68–72. 7 indexed citations

12.

Beer, Sabrina, et al.. (1976). Trisomy 13 Mosaic Presenting as Cleft Lip and Palate. Human Heredity. 26(5). 321–323. 7 indexed citations

13.

Fried, K., et al.. (1975). A Boy with 46, X, del(Y) Due to a <i>de novo</i> Mutation. Human Heredity. 25(6). 472–476. 6 indexed citations

14.

Fried, K., et al.. (1975). Autosomal recessive oculopharyngeal muscular dystrophy.. Journal of Medical Genetics. 12(4). 416–418. 20 indexed citations

15.

Fried, K., et al.. (1975). Thin ribs in neonatal myotonic dystrophy. Clinical Genetics. 7(5). 417–420. 14 indexed citations

16.

Fried, K., M Rosenblatt, G Mundel, & R. Krikler. (1975). Mental retardation and congenital malformations associated with a ring chromosome 6. Clinical Genetics. 7(3). 192–196. 38 indexed citations

17.

Fried, K.. (1974). Relatively high prevalence of the Meckel syndrome among Jews.. PubMed. 9(9). 1399–1399. 9 indexed citations

18.

Fried, K. & A.M. Davies. (1974). Some effects on the offspring of uncle-niece marriage in the Moroccan Jewish community in Jerusalem.. PubMed. 26(1). 65–72. 24 indexed citations

19.

Fried, K., et al.. (1974). A Meckel‐like syndrome?. Clinical Genetics. 5(1). 46–50. 13 indexed citations

20.

Fried, K.. (1972). Ectrodactyly‐ectodermal dysplasia‐clefting (EEC) syndrome. Clinical Genetics. 3(5). 396–400. 32 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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