K. Klinger
Impact in
-
- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
- Genetics top 0.5%
- Genetic and Kidney Cyst Diseases
- Genomic variations and chromosomal abnormalities
- Neurogenetic and Muscular Disorders Research
Papers in
-
- Renal and related cancers 7
- Genetics 37
- Genetic and Kidney Cyst Diseases 15
- Genomic variations and chromosomal abnormalities 12
- Genetic Syndromes and Imprinting 7
- Co-authors
- Anthony P. Shuber (7 shared papers)Brenda Richards (7 shared papers)Oxana Ibraghimov‐Beskrovnaya (9 shared papers)Seng H. Cheng (4 shared papers)Glenn T. Horn (6 shared papers)Richard J. Gregory (2 shared papers)Devra P. Rich (2 shared papers)Alan E. Smith (2 shared papers)
- Journals
- Genomics (6 papers)Human Molecular Genetics (6 papers)Cytogenetic and Genome Research (5 papers)American Journal of Obstetrics and Gynecology (4 papers)Proceedings of the National Academy of Sciences (4 papers)
- Partner nations
- United StatesPolandCanada
In The Last Decade
K. Klinger
103 papers receiving 6.9k citations
K. Klinger's Hit Papers
Peers
Comparison fields: 5 of 148
- Pediatrics, Perinatology and Child Health 1.6k
- Genetics 2.4k
- Genetics 675
- Pulmonary and Respiratory Medicine 1.7k
- Molecular Biology 2.9k
Countries citing papers authored by K. Klinger
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
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-authors
The 25 scholars most cited alongside K. Klinger, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 104 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Expression of cystic fibrosis transmembrane conductance regulator corrects defective chloride channel regulation in cystic fibrosis airway epithelial cells Hit paper breakdown → | 1990 | 615 |
| 2 | 2001 | 358 | |
| 3 | 1993 | 354 | |
| 4 | 2004 | 350 | |
| 5 | 1990 | 305 | |
| 6 | 1997 | 304 | |
| 7 | 2000 | 283 | |
| 8 | 2002 | 245 | |
| 9 | 2010 | 243 | |
| 10 | 2006 | 221 | |
| 11 | 1989 | 217 | |
| 12 | 1991 | 194 | |
| 13 | 1997 | 176 | |
| 14 | 1998 | 176 | |
| 15 | Rapid prenatal diagnosis of chromosomal aneuploidies by fluorescence in situ hybridization: clinical experience with 4,500 specimens. | 1993 | 172 |
| 16 | 2004 | 167 | |
| 17 | 2018 | 151 | |
| 18 | Linkage of cystic fibrosis to two tightly linked DNA markers: joint report from a collaborative study. | 1986 | 147 |
| 19 | 2000 | 144 | |
| 20 | 1988 | 141 |
About K. Klinger
K. Klinger is a scholar working on Molecular Biology, Genetics, Pulmonary and Respiratory Medicine, Pediatrics, Perinatology and Child Health and Surgery, having authored 104 papers that have together received 7.2k indexed citations. Recurring topics across this work include Cystic Fibrosis Research Advances (19 papers), Prenatal Screening and Diagnostics (17 papers), Genetic and Kidney Cyst Diseases (15 papers), Genomic variations and chromosomal abnormalities (12 papers), Tracheal and airway disorders (8 papers), Renal and related cancers (7 papers), Genetic Syndromes and Imprinting (7 papers) and Neonatal Respiratory Health Research (7 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (1.6k citations), Genetics (2.4k citations), Genetics (675 citations), Pulmonary and Respiratory Medicine (1.7k citations) and Molecular Biology (2.9k citations). K. Klinger has collaborated with scholars based in United States, Poland and Canada. Frequent co-authors include Anthony P. Shuber, Brenda Richards, Oxana Ibraghimov‐Beskrovnaya, Seng H. Cheng, Glenn T. Horn, Richard J. Gregory, Devra P. Rich, Alan E. Smith, Michael J. Welsh and Gregory M. Landes. Their work appears in journals such as Genomics, Human Molecular Genetics, Cytogenetic and Genome Research, American Journal of Obstetrics and Gynecology and Proceedings of the National Academy of Sciences.
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.