K. Klinger

16.4k total citations · 1 hit paper
103 papers, 6.9k citations indexed

About

K. Klinger is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, K. Klinger has authored 103 papers receiving a total of 6.9k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Molecular Biology, 37 papers in Genetics and 24 papers in Pulmonary and Respiratory Medicine. Recurrent topics in K. Klinger's work include Cystic Fibrosis Research Advances (19 papers), Prenatal Screening and Diagnostics (18 papers) and Genetic and Kidney Cyst Diseases (15 papers). K. Klinger is often cited by papers focused on Cystic Fibrosis Research Advances (19 papers), Prenatal Screening and Diagnostics (18 papers) and Genetic and Kidney Cyst Diseases (15 papers). K. Klinger collaborates with scholars based in United States, Canada and Poland. K. Klinger's co-authors include Anthony P. Shuber, Oxana Ibraghimov‐Beskrovnaya, Brenda Richards, Seng H. Cheng, Glenn T. Horn, Devra P. Rich, Richard J. Gregory, Alan E. Smith, Michael J. Welsh and Gregory M. Landes and has published in prestigious journals such as Nature, New England Journal of Medicine and Proceedings of the National Academy of Sciences.

In The Last Decade

K. Klinger

100 papers receiving 6.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Expression of cystic fibrosis transmembrane conductance regulator corrects defective chloride channel regulation in cystic fibrosis airway epithelial cells

1990 571 citations K. Klinger et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
K. Klinger United States	42	3.0k	2.4k	1.7k	1.6k	714	103	6.9k
John W. Belmont United States	60	6.6k 2.2×	5.3k 2.2×	1.3k 0.8×	826 0.5×	1.5k 2.2×	217	14.4k
Claude Férec France	55	3.9k 1.3×	2.8k 1.2×	2.7k 1.6×	665 0.4×	1.8k 2.5×	445	11.8k
Lap‐Chee Tsui Canada	57	5.8k 2.0×	2.8k 1.2×	4.7k 2.8×	740 0.5×	862 1.2×	145	12.6k
Magnus Nordenskjöld Sweden	57	4.8k 1.6×	3.7k 1.5×	1.2k 0.7×	711 0.4×	1.1k 1.5×	241	12.9k
Carmen Ayuso Spain	50	5.7k 1.9×	2.2k 0.9×	409 0.2×	681 0.4×	314 0.4×	351	9.0k
Andrea Superti‐Furga Switzerland	55	6.0k 2.0×	5.6k 2.3×	979 0.6×	608 0.4×	540 0.8×	300	11.8k
Stuart Schwartz United States	49	5.7k 1.9×	7.3k 3.1×	706 0.4×	2.3k 1.4×	330 0.5×	197	11.0k
R Harris United Kingdom	38	2.1k 0.7×	1.5k 0.6×	792 0.5×	742 0.5×	348 0.5×	174	7.2k
Noa Alon Canada	22	4.0k 1.3×	1.0k 0.4×	4.5k 2.7×	367 0.2×	773 1.1×	34	8.8k
John F. Tisdale United States	49	3.6k 1.2×	2.4k 1.0×	396 0.2×	1.3k 0.8×	3.1k 4.4×	267	10.0k

Countries citing papers authored by K. Klinger

Since Specialization

Citations

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

Fields of papers citing papers by K. Klinger

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

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

Lessard, Samuel, Michael J. Chao, Kadri Reis, et al.. (2024). Leveraging large-scale multi-omics evidences to identify therapeutic targets from genome-wide association studies. BMC Genomics. 25(1). 1111–1111. 4 indexed citations

Ruan, Jiapeng, Glenn S. Belinsky, Amir Akhavan, et al.. (2023). Osteonecrosis in Gaucher disease in the era of multiple therapies: Biomarker set for risk stratification from a tertiary referral center. eLife. 12. 7 indexed citations

Boddupalli, Chandra Sekhar, Shiny Nair, Glenn S. Belinsky, et al.. (2022). Neuroinflammation in neuronopathic Gaucher disease: Role of microglia and NK cells, biomarkers, and response to substrate reduction therapy. eLife. 11. 33 indexed citations

Han, Yingnan, Erin Teeple, Srinivas Shankara, et al.. (2021). Genome-Wide Polygenic Risk Score Identifies Individuals at Elevated Parkinson’s Disease Risk (4286). Neurology. 96(15_supplement). 2 indexed citations

Zhang, Mindy, Yi-Chien Chang, Srinivas Shankara, et al.. (2019). Characterization of the Peripheral Blood Transcriptome in Alemtuzumab-Treated Relapsing-Remitting Multiple Sclerosis Patients From the CARE-MS I and II Studies (P4.2-041). Neurology. 92(15_supplement). 1 indexed citations

Glascock, Jacqueline, Jacinda B. Sampson, Amanda Haidet-Phillips, et al.. (2018). Treatment Algorithm for Infants Diagnosed with Spinal Muscular Atrophy through Newborn Screening. Journal of Neuromuscular Diseases. 5(2). 145–158. 143 indexed citations

Natoli, Thomas A., Hervé Husson, Laurie A. Smith, et al.. (2012). Loss of GM3 synthase gene, but not sphingosine kinase 1, is protective against murine nephronophthisis-related polycystic kidney disease. Human Molecular Genetics. 21(15). 3397–3407. 33 indexed citations

Klinger, K., et al.. (2004). Politik und Verantwortung : zur Aktualität von Hannah Arendt. 1 indexed citations

Grody, Wayne W., Garry R. Cutting, K. Klinger, et al.. (2001). Laboratory standards and guidelines for population-based cystic fibrosis carrier screening. Genetics in Medicine. 3(2). 149–154. 326 indexed citations

10.

Foggensteiner, Lukas, A. Paul Bevan, Ruth Thomas, et al.. (2000). Cellular and Subcellular Distribution of Polycystin-2, the Protein Product of the PKD2 Gene. Journal of the American Society of Nephrology. 11(5). 814–827. 133 indexed citations

11.

Watnick, Terry, Bunyong Phakdeekitcharoen, Margaret Johnson, et al.. (1999). Mutation Detection of PKD1 Identifies a Novel Mutation Common to Three Families with Aneurysms and/or Very-Early-Onset Disease. The American Journal of Human Genetics. 65(6). 1561–1571. 74 indexed citations

12.

Gersen, Steven L., et al.. (1995). Rapid prenatal diagnosis of 14 cases of triploidy using fish with multiple probes. Prenatal Diagnosis. 15(1). 1–5. 12 indexed citations

13.

Reeves, Cynthia, et al.. (1994). An improved assay for the determination of Huntington`s disease allele size. The American Journal of Human Genetics. 55. 2 indexed citations

14.

Isada, Nelson B., Roderick F. Hume, Mark P. Johnson, et al.. (1994). Fluorescent in situ Hybridization and Second-Trimester Sonographic Anomalies: Uses and Limitations. Fetal Diagnosis and Therapy. 9(6). 367–370. 7 indexed citations

15.

Lerner, Terry J., Gabriella Wright, William R. Dackowski, et al.. (1992). Molecular analysis of human Chromosome 16 cosmid clones containing NotI sites. Mammalian Genome. 3(2). 92–100. 6 indexed citations

16.

Horn, Glenn T., et al.. (1991). Characterization and rapid analysis of the highly polymorphic VNTR locus D4S125 (YNZ32), closely linked to the huntington disease gene. Genomics. 9(2). 235–240. 15 indexed citations

17.

Price, James O., Sherman Elias, Stephen S. Wachtel, et al.. (1991). Prenatal diagnosis with fetal cells isolated from maternal blood by multiparameter flow cytometry. American Journal of Obstetrics and Gynecology. 165(6). 1731–1737. 182 indexed citations

18.

Williamson, R., A. Bowcock, K.K. Kidd, et al.. (1991). Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 24 of 27). Cytogenetic and Genome Research. 58(3-4). 1790–1800. 1 indexed citations

19.

Fujiwara, Takuya, K. Morgan, Robert H. Schwartz, et al.. (1989). Genealogical analysis of cystic fibrosis families and chromosome 7q RFLP haplotypes in the Hutterite Brethren.. PubMed. 44(3). 327–37. 30 indexed citations

20.

Klinger, K.. (1983). Cystic fibrosis in the Ohio Amish: Gene frequency and founder effect. Human Genetics. 65(2). 94–98. 28 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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