K. Klinger

16.4k citations

103 papers · 6.9k indexed · 1 hit paper · h-index 42

Genetics top 0.5%
- Genetic and Kidney Cyst Diseases 15
- Genomic variations and chromosomal abnormalities 12
- Genetic Syndromes and Imprinting 7
Pediatrics, Perinatology and Child Health top 0.5%
- Prenatal Screening and Diagnostics 18
Genetics top 1%
- Genetic and Kidney Cyst Diseases 15
- Genomic variations and chromosomal abnormalities 12
- Genetic Syndromes and Imprinting 7
Pulmonary and Respiratory Medicine top 1%
- Cystic Fibrosis Research Advances 19
- Tracheal and airway disorders 8
- Neonatal Respiratory Health Research 7
Molecular Biology top 2%
- Renal and related cancers 7

Co-authors: Anthony P. Shuber Oxana Ibraghimov‐Beskrovnaya Brenda Richards Seng H. Cheng Glenn T. Horn Michael J. Welsh Alan E. Smith Devra P. Rich
Cited by: Genetics Pediatrics, Perinatology and Child Health
Journals: Human Molecular Genetics (6 papers)Genomics (6 papers)Cytogenetic and Genome Research (6 papers)
Partner nations: United States Canada Poland

In The Last Decade

K. Klinger

100 papers receiving 6.6k citations

Hit Papers

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Peers

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

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.

Border = papers with K. Klinger Line = papers co-authored together K. Klinger links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Leveraging large-scale multi-omics evidences to identify therapeutic targets from genome-wide association studies BMC Genomics ·Samuel Lessard,Michael J. Chao,Kadri Reis,(unknown),Shashank Tayal,Deepak K. Rajpal,Q. WANG,Priit Palta,K. Klinger,Emanuele de Rinaldis,Khader Shameer,Clément Chatelain	2024	4
2	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 ·Mindy Zhang,Yi-Chien Chang,Srinivas Shankara,Alice K. Jacobs,J.F. GODIN,K. Klinger,Stephen F. Madden	2019	1
3	Treatment Algorithm for Infants Diagnosed with Spinal Muscular Atrophy through Newborn Screening Journal of Neuromuscular Diseases ·Jacqueline Glascock,Jacinda B. Sampson,Amanda Haidet-Phillips,Anne M. Connolly,Basil T. Darras,John Day,Richard S. Finkel,R. Rodney Howell,K. Klinger,Nancy L. Kuntz,Thomas W. Prior,Perry B. Shieh,Thomas O. Crawford,Douglas A. Kerr,Jill Jarecki	2018	143
4	Loss of GM3 synthase gene, but not sphingosine kinase 1, is protective against murine nephronophthisis-related polycystic kidney disease Human Molecular Genetics ·Thomas A. Natoli,Hervé Husson,YOHANES ARVIN WAHYU CHRISTIAWAN,Laurie A. Smith,Bing Wang,Cyntia Possídio,Nikolay O. Bukanov,Steven Ledbetter,K. Klinger,John P. Leonard,Oxana Ibraghimov‐Beskrovnaya	2012	33
5	CNS-targeted gene therapy improves survival and motor function in a mouse model of spinal muscular atrophy Journal of Clinical Investigation ·Marco A. Passini,Jie Bu,Eric M. Roskelley,Amy M. Richards,S. Pablo Sardi,Catherine R. O’Riordan,K. Klinger,Lamya S. Shihabuddin,Seng H. Cheng	2010	235
6	Inhibition of glycogen biosynthesis via mTORC1 suppression as an adjunct therapy for Pompe disease Molecular Genetics and Metabolism ·Karen M. Ashe,Kristin M. Taylor,S. N. Dubey,YongBok Lee,Ephraim Sheerin,A. Bochenska-Skalecka,K. Klinger,Patrick F. Finn,Christopher G. F. Cooper,Wei‐Lien Chuang,John Marshall,John M. McPherson,Robert J. Mattaliano,Seng H. Cheng,Ronald K. Scheule,Rodney J. Moreland	2010	40
7	Knockdown of human deubiquitinase PSMD14 induces cell cycle arrest and senescence Experimental Cell Research ·Annette T. Byrne,D.R. Watson,Paul Mason,J. Jurkievich,Michael R. Dufault,Yinyin Huang,A DI PIETRO,K. Gerbosch,Mindy Zhang,Kara Carter,Tatiana Gladysheva,Beverly A. Teicher,Geo. S. Eyster,Michael L. Booker,Mark A. Goldberg,K. Klinger,James W. Lillie,Stephen F. Madden,Yide Jiang	2009	54
8	Politik und Verantwortung : zur Aktualität von Hannah Arendt Akihiro Kurosawa,K. Klinger,Hannah Arendt,Cynthia Caetano	2004	1
9	Actin‐dependent motility of melanosomes from fish retinal pigment epithelial (RPE) cells investigated using in vitro motility assays Cell Motility and the Cytoskeleton ·Babakano Ahmed,B. Harand,Paul Basciano,O BLITZ,Robert D. Williams,P. Damiani,R. BITTMANN,C F Fox,Bonnie J. Stewart,Ma. Criselda B. Macatangay,Lailatun Nasucha,K. Klinger,James R. Sellers,Eman Awad Bedir Elakhder	2004	13
10	Laboratory standards and guidelines for population-based cystic fibrosis carrier screening Genetics in Medicine ·Wayne W. Grody,Garry R. Cutting,K. Klinger,C. Sue Richards,Michael S. Watson,Robert J. Desnick	2001	326
11	Cellular and Subcellular Distribution of Polycystin-2, the Protein Product of the PKD2 Gene Journal of the American Society of Nephrology ·Lukas Foggensteiner,A. Paul Bevan,Ruth Thomas,Nicholas Coleman,Catherine A. Boulter,John R. Bradley,Oxana Ibraghimov‐Beskrovnaya,K. Klinger,Richard Sandford	2000	133
12	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 ·Terry Watnick,Bunyong Phakdeekitcharoen,Margaret Johnson,Steve Ditmeyer,Mei Wang,Gary Briefel,K. Klinger,William J. Kimberling,Patricia A. Gabow,Gregory G. Germino	1999	74
13	Generation of a transcriptional map for a 700-kb region surrounding the polycystic kidney disease type 1 (PKD1) and tuberous sclerosis type 2 (TSC2) disease genes on human chromosome 16p3.3. Genome Research ·Timothy C. Burn,Timothy D. Connors,Terence J. Van Raay,William R. Dackowski,John M. Millholland,K. Klinger,Gregory M. Landes	1996	20
14	Rapid prenatal diagnosis of 14 cases of triploidy using fish with multiple probes Prenatal Diagnosis ·Steven L. Gersen,Zenebe Negeri,K. Klinger,Brian E. Ward	1995	12
15	An improved assay for the determination of Huntington`s disease allele size The American Journal of Human Genetics ·Cynthia Reeves,K. Klinger,Fachbereich Bio	1994	2
16	Fluorescent in situ Hybridization and Second-Trimester Sonographic Anomalies: Uses and Limitations Fetal Diagnosis and Therapy ·Nelson B. Isada,Roderick F. Hume,Seong Wook Park,Mark P. Johnson,K. Klinger,Mark I. Evans,Brian E. Ward	1994	7
17	Intra- and extragenic marker haplotypes of CFTR mutations in cystic fibrosis families Human Genetics ·Thilo Dörk,Thomas Neumann,Ulrich Wulbrand,Brigitte Wulf,Nanette Kälin,S. Lu,Supreet Mohanty,H. Guillermit,Claude Férec,Glenn T. Horn,K. Klinger,Bat-Sheva Kerem,Julian Zielenski,L.-C. Tsui,Burkhard Tümmler	1992	58
18	Multicolor fluorescence in situ hybridization for the simultaneous detection of probe sets for chromosomes 13, 18, 21, X and Y in uncultured amniotic fluid cells Human Molecular Genetics ·Thomas Ried,Greg Landes,William R. Dackowski,K. Klinger,David C. Ward	1992	91
19	Characterization and rapid analysis of the highly polymorphic VNTR locus D4S125 (YNZ32), closely linked to the huntington disease gene Genomics ·Manoela Lima Maciel,Glenn T. Horn,竹森民樹,K. Klinger	1991	15
20	Prenatal diagnosis with fetal cells isolated from maternal blood by multiparameter flow cytometry American Journal of Obstetrics and Gynecology ·James O. Price,Sherman Elias,Stephen S. Wachtel,K. Klinger,Michael E. Dockter,Avirachan T. Tharapel,L.P. Shulman,Owen P. Phillips,Carole M. Meyers,Wen Zhi-zhuan,Joe Leigh Simpson	1991	182

About K. Klinger

K. Klinger is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Pulmonary and Respiratory Medicine, having authored 103 papers that have together received 6.9k indexed citations. Recurring topics across this work include Cystic Fibrosis Research Advances (19 papers), Prenatal Screening and Diagnostics (18 papers), Genetic and Kidney Cyst Diseases (15 papers), Genomic variations and chromosomal abnormalities (12 papers), Tracheal and airway disorders (8 papers), Genetic Syndromes and Imprinting (7 papers), Neonatal Respiratory Health Research (7 papers) and Renal and related cancers (7 papers). The work is most often cited by research in Genetics (2.4k citations), Pediatrics, Perinatology and Child Health (1.6k citations) and Genetics (714 citations). K. Klinger has collaborated with scholars based in United States, Canada and Poland. Frequent co-authors include Anthony P. Shuber, Oxana Ibraghimov‐Beskrovnaya, Brenda Richards, Seng H. Cheng, Glenn T. Horn, Michael J. Welsh, Alan E. Smith, Devra P. Rich, Richard J. Gregory and Gregory M. Landes. Their work appears in journals such as Human Molecular Genetics, Genomics, 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.

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