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Most cited papers from Cambridge Collaborative (United States)

What are the most cited papers from Cambridge Collaborative (United States)?

The most cited paper from Cambridge Collaborative (United States) is "Virus-Enabled Synthesis and Assembly of Nanowires for Lithium Ion Battery Electrodes" (Ki Tae Nam, Dong‐Wan Kim, Pil Jin Yoo et al., 2006), with 1,856 citations. Next come "Patterns of linkage disequilibrium in the human genome" (1,152) and "A genetic linkage map of the human genome" (913).

Showing 50 of 60 papers. Every paper with more than 33 citations is listed.

Most cited papers, sortable by citations and release date
#Paper
1 Virus-Enabled Synthesis and Assembly of Nanowires for Lithium Ion Battery Electrodes Ki Tae Nam, Dong‐Wan Kim, Pil Jin Yoo et al. · Science 6 Apr 2006 1,856
2 Patterns of linkage disequilibrium in the human genome Kristin Ardlie, Leonid Kruglyak, Mark T. Seielstad · Nature Reviews Genetics Review Apr 2002 1,152
3 A genetic linkage map of the human genome H DONISKELLER · Cell Oct 1987 913
4 Genetic Association of the R620W Polymorphism of Protein Tyrosine Phosphatase PTPN22 with Human SLE Chieko Kyogoku et al. · The American Journal of Human Genetics Open access 3 Aug 2004 672
5 The yeast secretory pathway is perturbed by mutations in PMR1, a member of a Ca2+ ATPase family Hans K. Rudolph, Adam Antebi, Gerald R. Fink et al. · Cell Jul 1989 537
6 Demonstrating stratification in a European American population Catarina D. Campbell, Elizabeth L. Ogburn, Kathryn L. Lunetta et al. · Nature Genetics 24 Jul 2005 450
7 A polymorphic DNA marker linked to cystic fibrosis is located on chromosome 7 Robert G. Knowlton, Odile Cohen‐Haguenauer, N'Guyen Van Cong et al. · Nature Nov 1985 334
8 Effective and fibrin-specific clot lysis by a zymogen precursor form of urokinase (pro-urokinase). A study in vitro and in two animal species. Victor Gurewich, Ralph Pannell, Shirley C. Louie et al. · Journal of Clinical Investigation Open access Jun 1984 310
9 Recurrent mutations in haemophilia A give evidence for CpG mutation hotspots Hagop Youssoufian, Haig H. Kazazian, Deborah G. Phillips et al. · Nature Nov 1986 268
10 Autosomal dominant retinitis pigmentosa (ADRP): Localization of an ADRP gene to the long arm of chromosome 3 Peter McWilliam, Gwyneth Jane Farrar, Paul F. Kenna et al. · Genomics Oct 1989 247
11 Testing for Population Subdivision and Association in Four Case-Control Studies Kristin Ardlie, Kathryn L. Lunetta, Mark T. Seielstad · The American Journal of Human Genetics Open access Aug 2002 223
12 Effective Pulmonary Ventilation with Small-Volume Oscillations At High Frequency Arthur S. Slutsky, Jeffrey M. Drazen, Roland H. Ingram et al. · Science Aug 1980 190
13 Understanding the benefit and costs of communities of practice David R. Millen, Michael A. Fontaine, Michael J. Muller · Communications of the ACM Apr 2002 189
14 Identification of nonlinear structural elements by force-state mapping Edward F. Crawley, Allan C. Aubert · AIAA Journal 1986 178
15 The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: Implications for a role of chromatin structure in the pathogenesis of the disease Sara T. Winokur, Ulla Bengtsson, Julie Feddersen et al. · Chromosome Research May 1994 154
16 A SECOND GENETIC LOCUS FOR AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE G. Romeo, Gianna Costa, Luigi Catizone et al. · The Lancet Jul 1988 141
17 Preferential mutation of the neurofibromatosis type 1 gene in paternally derived chromosomes Karen G. Stephens, Lucille M. Kayes, VincentM. Riccardi et al. · Human Genetics 1992 133
18 Xq–Yq interchange resulting in supernormal X-linked gene expression in severely retarded males with 46,XYq- karyotype Bruce T. Lahn, Nancy Ma, W. Roy Breg et al. · Nature Genetics Nov 1994 116
19 Spin Filter Perfusion System for High Density Cell Culture: Production of Recombinant Urinary Type Plasminogen Activator in CHO Cells George C. Avgerinos, Denis Drapeau, Jeff S. Socolow et al. · Nature Biotechnology 1990 111
20 Categorising trajectories and individual item changes of the North Star Ambulatory Assessment in patients with Duchenne muscular dystrophy Francesco Muntoni, Joana Domingos, Adnan Yousaf Manzur et al. · PLoS ONE Open access 3 Sep 2019 105
21 Identification of a new variant CYP2D6 allele with a single base deletion in exon 3 and its association with the poor metabolizer phenotype Richa Saxena, G. L. Shaw, Mary V. Relling et al. · Human Molecular Genetics 1994 102
22 Genomic organization of the mycobacterial sigma gene cluster Laurence Doukhan, Mima Predich, Gopalan M. Nair et al. · Gene Open access 1995 100
23 Concerted deletions and inversions are caused by mitotic recombination between delta sequences in Saccharomyces cerevisiae. Rodney J. Rothstein, Cynthia Helms, Nurit Rosenberg · Molecular and Cellular Biology Open access Mar 1987 99
24 Estrogen Receptor α Gene Variation Is Associated With Risk of Myocardial Infarction in More Than Seven Thousand Men From Five Cohorts Amanda M. Shearman, Jackie A. Cooper, Paul J. Kotwinski et al. · Circulation Research 17 Feb 2006 93
25 Mechanical Response of the Lungs at High Frequencies J. J. Fredberg, A. Hoenig · Journal of Biomechanical Engineering May 1978 92
26 Alleles carried at positions ?819 and ?592 of the IL10 promoter affect transcription following stimulation of peripheral blood cells with Streptococcus pneumoniae Suzanna E.L. Temple, Esther Lim, Karey Cheong et al. · Immunogenetics Dec 2003 85
27 Incidence and expression of the N1303K mutation of the cystic fibrosis (CFTR) gene Lucy R. Osborne et al. · Human Genetics Aug 1992 79
28 Amplification of large artificial chromosomes. Douglas R. Smith, A.P. Smyth, Donald T. Moir · Proceedings of the National Academy of Sciences Open access Nov 1990 72
29 Individualized Prediction of Changes in 6-Minute Walk Distance for Patients with Duchenne Muscular Dystrophy Nathalie Goemans, M. vanden Hauwe, James Edward Signorovitch et al. · PLoS ONE Open access 13 Oct 2016 67
30 The CEPH consortium primary linkage map of human chromosome 10 Raymond L. White, Jean‐Marc Lalouel, Yusuke Nakamura et al. · Genomics Mar 1990 67
31 Identification of more than 500 RFLPs by screening random genomic clones. James W. Schumm, Robert G. Knowlton, Jeffrey C. Braman et al. · PubMed 1988 64
32 Molecular cloning and characterization of double-stranded cDNA coding for bovine chymosin Donald T. Moir, Jen-i Mao, James W. Schumm et al. · Gene Jul 1982 61
33 Glycosylation and secretion of human alpha-1-antitrypsin by yeast Donald T. Moir, Dennis R. Dumais · Gene 1987 61
34 Principles and Standards: Developing Computational Fluency with Whole Numbers Susan Jo Russell · Teaching Children Mathematics Nov 2000 60
35 Formulation of SEA parameters using mobility functions Jerome E. Manning · Philosophical Transactions of the Royal Society of London Series A Physical and Engineering Sciences 15 Mar 1994 59
36 Origin and character of vascular murmurs: Model studies Jeffrey J. Fredberg · The Journal of the Acoustical Society of America Apr 1977 57
37 Mapping the facioscapulohumeral muscular dystrophy gene is complicated by chromosome 4q35 recombination events Barbara Weiffenbach, JoAnn Dubois, Diane Storvick et al. · Nature Genetics Jun 1993 56
38 Discrete lung sounds: Crackles (rales) as stress–relaxation quadrupoles Jeffrey J. Fredberg, Stephen K. Holford · The Journal of the Acoustical Society of America Mar 1983 56
39 Germline RET mutations in MEN 2A and FMTC and their detection by simple DNA diagnostic tests Feiyu Xue, Hong Ping Yu, L. Herbert Maurer et al. · Human Molecular Genetics 1994 53
40 An extremely polymorphic locus on the short arm of the human X chromosome with homology to the long arm of the Y chromosome Robert G. Knowlton, Carrie A. Nelson, Valerie A. Brown et al. · Nucleic Acids Research Open access 1989 52
41 Lysergic Acid Diethylamide: Radioimmunoassay Alison Taunton-Rigby, S. Sher, Paul R. Kelley · Science 13 Jul 1973 50
42 Fanconi anemia: Evidence for linkage heterogeneity on chromosome 20q W. Mann, Vijayanagaram S. Venkatraj, Robert G. Allen et al. · Genomics Feb 1991 48
43 Characterization of a nonglycosylated single chain urinary plasminogen activator secreted from yeast. Laurence M. Melnick, Brian G. Turner, Patricia Puma et al. · Journal of Biological Chemistry Open access 1990 46
44 Mechanisms of Radiosensitization in Bromodeoxyuridine-substituted Cells Carol F. Webb, George D.D. Jones, John Francis Ward et al. · International Journal of Radiation Biology 1993 41
45 Adenylate cyclase activity in normal and leukemic human leukocytes as determined by a radioimmunoassay for cyclic AMP PETER R. POLGAR, José Luis del Castillo Pardo de Vera, Paul R. Kelley et al. · Biochimica et Biophysica Acta (BBA) - General Subjects 28 Feb 1973 41
46 Real-world and natural history data for drug evaluation in Duchenne muscular dystrophy: suitability of the North Star Ambulatory Assessment for comparisons with external controls Francesco Muntoni, James Edward Signorovitch, Gautam Sajeev et al. · Neuromuscular Disorders Open access 25 Feb 2022 40
47 [14] DNA sequencing with direct transfer electrophoresis and nonradioactive detection Peter Richterich, George M. Church · Methods in enzymology on CD-ROM/Methods in enzymology Book chapter 1993 40
48 Kidney Plasminogen Activator: A Precursor Form of Human Urokinase With High Fibrin Affinity Tadahiko Kohno, Peggy Hopper, Jay S. Lillquist et al. · Nature Biotechnology Jul 1984 40
49 The distributed response of complex branching duct networks J. J. Fredberg, Jennifer A. Moore · The Journal of the Acoustical Society of America Mar 1978 39
50 Characterization of the intrinsic fibrinolytic properties of pro-urokinase through a study of plasmin-resistant mutant forms produced by site-specific mutagenesis of lysine(158). Victor Gurewich, Ralph Pannell, ROBERT J. BROEZE et al. · Journal of Clinical Investigation Open access Dec 1988 38

Citations are OpenAlex's own counts, from its 2026-09-23 snapshot, so the ranking can differ from Google Scholar or Web of Science. A paper is listed for an institution when any of its authors gave it as an affiliation; retracted papers and papers whose citation count cannot be traced to citing works are left out, and a preprint and the article it became are shown once. Release dates are OpenAlex's: where a source gave only a month or a year, that is what is shown. How the lists are chosen.