C. C. Lin

719 total citations
19 papers, 537 citations indexed

About

C. C. Lin is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, C. C. Lin has authored 19 papers receiving a total of 537 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 10 papers in Genetics and 9 papers in Plant Science. Recurrent topics in C. C. Lin's work include Chromosomal and Genetic Variations (9 papers), Genomic variations and chromosomal abnormalities (7 papers) and Prenatal Screening and Diagnostics (3 papers). C. C. Lin is often cited by papers focused on Chromosomal and Genetic Variations (9 papers), Genomic variations and chromosomal abnormalities (7 papers) and Prenatal Screening and Diagnostics (3 papers). C. C. Lin collaborates with scholars based in Canada, United States and United Kingdom. C. C. Lin's co-authors include Charles Lee, M.A. Ferguson‐Smith, Rachel Wevrick, Richard B. Fisher, Ramakrishnan Sasi, Michael R. Waterman, Jeremy S.D. Winter, J. Bamforth, Frances Harley and Norma Leonard and has published in prestigious journals such as Genomics, Human Genetics and Chromosoma.

In The Last Decade

C. C. Lin

19 papers receiving 519 citations

Peers

Countries citing papers authored by C. C. Lin

Since Specialization

Citations

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

Fields of papers citing papers by C. C. Lin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of C. C. Lin

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

19 of 19 papers shown

#	Work	Indexed citations
1	Proof of concept: Pull down assay using bovine serum albumin and an immunomodulator small molecule 2023 ·Heliyon ·Yasser Tabana, C. C. Lin, Dinesh Babu, (unknown), (unknown), Tae Chul Moon, Arno G. Siraki, Shokrollah Elahi, Richard P. Fahlman, F. G. West, Khaled Barakat	1
2	Direct visualization of the genomic distribution and organization of two cervid centromeric satellite DNA families 2000 ·Cytogenetic and Genome Research ·(unknown), (unknown), Te-Cheng Hsu, (unknown), C. C. Lin	18
3	Terminal deletion of chromosome 10q at band 26.1: Follow-up in an adolescent male with high-output renal failure from congenital obstructive uropathy 1999 ·American Journal of Medical Genetics ·Norma Leonard, Frances Harley, C. C. Lin	17
4	Defining the anatomy of the Rangifer tarandus sex chromosomes 1998 ·Chromosoma ·Charles Lee, Darren K. Griffin, Peter C. O’Brien, Fengtang Yang, C. C. Lin, M.A. Ferguson‐Smith	14
5	Human centromeric DNAs 1997 ·Human Genetics ·Charles Lee, Rachel Wevrick, Richard B. Fisher, M.A. Ferguson‐Smith, C. C. Lin	191
6	DK phocomelia phenotype (von Voss-Cherstvoy syndrome) caused by somatic mosaicism for del(13q) 1997 ·American Journal of Medical Genetics ·J. Bamforth, C. C. Lin	17
7	Conservation of a 31-bp bovine subrepeat in centromeric satellite DNA monomers ofCervus elaphus and other cervid species 1996 ·Chromosome Research ·Charles Lee, C. C. Lin	19
8	Isolation and identification of a novel tandemly repeated DNA sequence in the centromeric region of human chromosome 8 1993 ·Chromosoma ·C. C. Lin, Ramakrishnan Sasi, (unknown), (unknown)	30
9	Localization of the human CYP17 gene (cytochrome P45017α) to 10q24.3 by fluorescence in situ hybridization and simultaneous chromosome banding 1992 ·Genomics ·(unknown), Ramakrishnan Sasi, Charles Lee, Jeremy S.D. Winter, Michael R. Waterman, C. C. Lin	83
10	Assignment of the human muscle adenine nucleotide translocator gene (ANT1) to 4q35 by fluorescence in situ hybridization 1992 ·Cytogenetic and Genome Research ·(unknown), (unknown), C. C. Lin	8
11	New evidence for tandem chromosome fusions in the karyotypic evolution of Asian muntjacs 1991 ·Chromosoma ·C. C. Lin, Ramakrishnan Sasi, (unknown), (unknown)	53
12	Chromosome aberrations and oncogene alterations in two new breast tumor cell lines 1991 ·Cancer Genetics and Cytogenetics ·Ramakrishnan Sasi, (unknown), (unknown), (unknown), (unknown), C. C. Lin	8
13	Apparent lack of telomere sequences on double minute chromosomes 1990 ·Cancer Genetics and Cytogenetics ·C. C. Lin, Julianne Meyne, (unknown), Robert K. Moyzis	18
14	Chromosome localization of two human serine protease genes to region 14q11.2→q12 by in situ hybridization 1990 ·Cytogenetic and Genome Research ·C. C. Lin, Michael Meier, Ole E. Sørensen, Ramakrishnan Sasi, (unknown), R. Chris Bleackley	4
15	Multiple, variable‐sized, minute marker chromosomes 1988 ·American Journal of Medical Genetics ·Joe J. Hoo, C. C. Lin, John M. Optiz	5
16	Cytogenetic and biological characterization of two new human plasma cell lines 1987 ·Cancer Genetics and Cytogenetics ·Larry W. Brox, Andrew R. Belch, (unknown), (unknown), Marc De Braekeleer, C. C. Lin	5
17	A case of M2 acute myeloblastic leukemia associated with an interstitial 9q deletion 1987 ·Cancer Genetics and Cytogenetics ·C. C. Lin, Marc De Braekeleer, Wai S. Etches, (unknown)	7
18	Familial paracentric inversions inv(2)(q31q35) and inv(8)(q22.3q24.13) ascertained through reproductive abnormalities 1987 ·Human Genetics ·C. C. Lin, Phyllis E. Bowen, Joe J. Hoo	11
19	The meiotic segregation of human sperm chromosomes in two men with accessory marker chromosomes 1986 ·American Journal of Medical Genetics ·Renée H. Martin, Kathy Hildebrand, (unknown), (unknown), Alfred Rademaker, Patrick Taylor, C. C. Lin, John M. Opitz	28

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.

Explore authors with similar magnitude of impact