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Institution · Transgenomic (United States)

Most cited papers from Transgenomic (United States)

Transgenomic (United States)

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

The most cited paper from Transgenomic (United States) is "The Ink4/Arf locus is a barrier for iPS cell reprogramming" (Han Li, Manuel Collado, Aránzazu Villasante et al., 2009), with 976 citations. Next come "Mutations of the Cardiac Ryanodine Receptor (RyR2) Gene in Familial Polymorphic Ventricular Tachycardia" (739) and "Improved Identification of von Hippel-Lindau Gene Alterations in Clear Cell Renal Tumors" (611).

Showing 50 of 61 papers. Every paper with more than 39 citations is listed.

Most cited papers, sortable by citations and release date
#Paper
1 The Ink4/Arf locus is a barrier for iPS cell reprogramming Han Li, Manuel Collado, Aránzazu Villasante et al. · Nature Open access Aug 2009 976
2 Mutations of the Cardiac Ryanodine Receptor (RyR2) Gene in Familial Polymorphic Ventricular Tachycardia Päivi J. Laitinen, Kevin M. Brown, Kirsi Piippo et al. · Circulation Open access 30 Jan 2001 739
3 Improved Identification of von Hippel-Lindau Gene Alterations in Clear Cell Renal Tumors Michael L. Nickerson et al. · Clinical Cancer Research Open access Aug 2008 611
4 Natural history of dilated cardiomyopathy due to lamin A/C gene mutations Matthew R. Taylor, Pamela R. Fain, Gianfranco Sinagra et al. · Journal of the American College of Cardiology Open access Mar 2003 502
5 Eradication of Tumors through Simultaneous Ablation of CD276/B7-H3-Positive Tumor Cells and Tumor Vasculature Steven Seaman et al. · Cancer Cell Open access Apr 2017 463
6 miR-34 miRNAs provide a barrier for somatic cell reprogramming Yong Jin Choi, Chao‐Po Lin, Jaclyn J. Ho et al. · Nature Cell Biology Open access 23 Oct 2011 384
7 Mutation detection using Surveyor™ nuclease Peter Qiu, Harini Shandilya, James M. D'Alessio et al. · BioTechniques Open access Apr 2004 308
8 Distinguishing Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia–Associated Mutations From Background Genetic Noise Jamie D. Kapplinger, Andrew Paul Landstrom, Benjamin A. Salisbury et al. · Journal of the American College of Cardiology Open access Jun 2011 304
9 The JAK2 V617F mutation occurs in hematopoietic stem cells in polycythemia vera and predisposes toward erythroid differentiation Catriona H. M. Jamieson, Jason R. Gotlib, Jeffrey A. Durocher et al. · Proceedings of the National Academy of Sciences Open access 7 Apr 2006 287
10 Upregulation of Poly (ADP-Ribose) Polymerase-1 (PARP1) in Triple-Negative Breast Cancer and Other Primary Human Tumor Types Valeria Ossovskaya, Ingrid Chou Koo, Eric Peter Kaldjian et al. · Genes & Cancer Open access Aug 2010 284
11 CACNA1C (Cav1.2) in the pathophysiology of psychiatric disease Shambhu Bhat, David T. Dao, Chantelle E. Terrillion et al. · Progress in Neurobiology Open access 15 Jun 2012 282
12 New evidence that a large proportion of human blood plasma cell-free DNA is localized in exosomes M. Rohan Fernando, Chao Yun Jiang, Gary D. Krzyzanowski et al. · PLoS ONE Open access 29 Aug 2017 273
13 Glycogen synthase kinase 3β missplicing contributes to leukemia stem cell generation Annelie E. Abrahamsson, Ifat Geron, Jason R. Gotlib et al. · Proceedings of the National Academy of Sciences Open access 23 Feb 2009 244
14 COX-2 Inhibition Potentiates Antiangiogenic Cancer Therapy and Prevents Metastasis in Preclinical Models Lihong Xu, Janine Stevens, Mary Beth Hilton et al. · Science Translational Medicine Open access 25 Jun 2014 228
15 A Rapid and Sensitive Enzymatic Method for Epidermal Growth Factor Receptor Mutation Screening Pasi Antero Janne, Ana M. Borras, Yanan Kuang et al. · Clinical Cancer Research Feb 2006 219
16 Three‐dimensional domain swapping in the folded and molten‐globule states of cystatins, an amyloid‐forming structural superfamily Rosemary A. Staniforth, Silva Giannini, Lee D. Higgins et al. · The EMBO Journal Open access 3 Sep 2001 203
17 The TCF-1 and LEF-1 Transcription Factors Have Cooperative and Opposing Roles in T Cell Development and Malignancy Shuyang Yu, Xinyuan Zhou, Farrah C. Steinke et al. · Immunity Open access 25 Oct 2012 195
18 Culture-Independent Identification of Pathogenic Bacteria and Polymicrobial Infections in the Genitourinary Tract of Renal Transplant Recipients Eugen Domann, George Hong, Can Imirzalioglu et al. · Journal of Clinical Microbiology Open access Dec 2003 177
19 Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records Sara L. Van Driest et al. · JAMA Open access 5 Jan 2016 176
20 Hydrophobic surfaces for enhanced differentiation of embryonic stem cell-derived embryoid bodies Bahram Bob Valamehr, Steven John Jonas, Julien Polleux et al. · Proceedings of the National Academy of Sciences Open access 12 Sep 2008 158
21 GPR124 Functions as a WNT7-Specific Coactivator of Canonical β-Catenin Signaling Ekaterina N. Posokhova, Animesh Shukla, Steven Seaman et al. · Cell Reports Open access 31 Dec 2014 157
22 Detection of Single-Nucleotide Polymorphisms with the WAVE™ DNA Fragment Analysis System Alexander I. Kuklin, KIMBERLY MUNSON, Douglas Thomas Gjerde et al. · Genetic Testing 1997 151
23 Sporadic hybrid oncocytic/chromophobe tumor of the kidney: a clinicopathologic, histomorphologic, immunohistochemical, ultrastructural, and molecular cytogenetic study of 14 cases Fredrik Petersson, Zoran Gatalica, Petr Grossmann et al. · Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin 18 Mar 2010 149
24 Overcoming Acquired Resistance to AZD9291, A Third-Generation EGFR Inhibitor, through Modulation of MEK/ERK-Dependent Bim and Mcl-1 Degradation Puyu Shi, You-Take Oh, Liang Hao Deng et al. · Clinical Cancer Research Open access Aug 2017 145
25 Developmental Competence of Juvenile Calf Oocytes In Vitro and In Vivo: Influence of Donor Animal Variation and Repeated Gonadotropin Stimulation1 Maneesh Taneja, Peter E.J. Bols, Anneleen Van de Velde et al. · Biology of Reproduction 2000 136
26 Selective Inhibition of JAK2-Driven Erythroid Differentiation of Polycythemia Vera Progenitors Ifat Geron, Annelie E. Abrahamsson, Charlene F. Barroga et al. · Cancer Cell Open access Apr 2008 135
27 eIF2α Phosphorylation-Dependent Translation in CA1 Pyramidal Cells Impairs Hippocampal Memory Consolidation without Affecting General Translation Zhi‐Hong Jiang, Juan Emilio Belforte, Yuan Lü et al. · Journal of Neuroscience Open access 17 Feb 2010 127
28 Mutations in mitochondrial DNA polymerase-γ promote breast tumorigenesis Keshav K. Singh, Ayyasamy Vanniarajan, Kjerstin M. Owens et al. · Journal of Human Genetics Open access 24 Jul 2009 123
29 Establishment of Perineural Invasion Models and Analysis of Gene Expression Revealed an Invariant Chain (CD74) as a Possible Molecule Involved in Perineural Invasion in Pancreatic Cancer Norimasa Koide, Taketo Yamada, Rie Shibata et al. · Clinical Cancer Research 15 Apr 2006 112
30 Mutations in theUBIAD1Gene on Chromosome Short Arm 1, Region 36, Cause Schnyder Crystalline Corneal Dystrophy Jayne S. Weiss, Howard S. Kruth, Helena Kuivaniemi et al. · Investigative Ophthalmology & Visual Science 25 Oct 2007 103
31 Enhanced Classification of Brugada Syndrome–Associated and Long-QT Syndrome–Associated Genetic Variants in the SCN5A -Encoded Na v 1.5 Cardiac Sodium Channel Jamie D. Kapplinger, John R. Giudicessi, Dan Ye et al. · Circulation Cardiovascular Genetics Open access 22 Apr 2015 99
32 RNA analysis by ion-pair reversed-phase high performance liquid chromatography Arezou Azarani · Nucleic Acids Research Open access 15 Jan 2001 96
33 MLL4 prepares the enhancer landscape for Foxp3 induction via chromatin looping Katarzyna Placek, Gangqing Hu, Kairong Cui et al. · Nature Immunology Open access 31 Jul 2017 95
34 Mitochondrial Disease Sequence Data Resource (MSeqDR): A global grass-roots consortium to facilitate deposition, curation, annotation, and integrated analysis of genomic data for the mitochondrial disease clinical and research communities Marni J. Falk et al. · Molecular Genetics and Metabolism Open access 4 Dec 2014 92
35 NATURAL COMPOUNDS IN DRUG DISCOVERY. BIOLOGICAL ACTIVITY AND NEW TRENDS IN THE CHEMISTRY OF ISOQUINOLINE ALKALOIDS Victor G. Kartsev · Medicinal Chemistry Research Jul 2004 76
36 The Use of Denaturing High-Performance Liquid Chromatography (DHPLC) for the Analysis of Genetic Variations: Impact for Diagnostics and Pharmacogenetics Felix W. Frueh, Mario Noyer-Weidner · Clinical Chemistry and Laboratory Medicine (CCLM) 25 Jan 2003 74
37 A synthetic DNA encoding a modified human urokinase resistant to inhibition by serum plasminogen activator inhibitor D. Adams, Louise Griffin, W.R. Nachajko et al. · Journal of Biological Chemistry Open access May 1991 68
38 Efficacy of Porcine Gonadotropins for Repeated Stimulation of Ovarian Activity for Oocyte Retrieval and In Vitro Embryo Production and Cryopreservation in Siberian Tigers (Panthera tigris altaica)1 Elizabeth G. Crichton, Elliott Bedows, Amanda K. Miller-Lindholm et al. · Biology of Reproduction 2003 66
39 Phylogenetic and Physicochemical Analyses Enhance the Classification of Rare Nonsynonymous Single Nucleotide Variants in Type 1 and 2 Long-QT Syndrome John R. Giudicessi, Jamie D. Kapplinger, David J. Tester et al. · Circulation Cardiovascular Genetics Open access 5 Sep 2012 64
40 A phase I trial of immunotherapy with intratumoral adenovirus-interferon-gamma (TG1041) in patients with malignant melanoma Alok A. Khorana, Joseph D. Rosenblatt, Deepak M. Sahasrabudhe et al. · Cancer Gene Therapy Apr 2003 63
41 Targeted exome sequencing for mitochondrial disorders reveals high genetic heterogeneity Jeana T. DaRe, Valeria Vasta, John S. Penn et al. · BMC Medical Genetics Open access 11 Nov 2013 63
42 NRAS mutations with low allele burden have independent prognostic significance for patients with lower risk myelodysplastic syndromes Derek M. Murphy, Rafael L. Bejar, Kristen E. Stevenson et al. · Leukemia Open access 27 May 2013 59
43 Conditional deletion of nonmuscle myosin II-A in mouse tongue epithelium results in squamous cell carcinoma Mary Anne Conti, Anthony D. Saleh, Lauren Brinster et al. · Scientific Reports Open access 15 Sep 2015 58
44 Detection of ?-galactosidase a mutations causing fabry disease by denaturing high performance liquid chromatography Junaid Shabbeer, Misi L. Robinson, Robert J. Desnick · Human Mutation 2005 57
45 Distinguishing Hypertrophic Cardiomyopathy-Associated Mutations from Background Genetic Noise Jamie D. Kapplinger, Andrew Paul Landstrom, Johan Martijn Bos et al. · Journal of Cardiovascular Translational Research Open access 7 Feb 2014 57
46 Telomeric TERB1–TRF1 interaction is crucial for male meiosis Juanjuan Long, Chenhui Huang, Yanyan Chen et al. · Nature Structural & Molecular Biology Open access 30 Oct 2017 56
47 Evaluating the role of connexin43 in congenital heart disease: Screening for mutations in patients with outflow tract anomalies and the analysis of knock-in mouse models Guo-Ying Huang, Lijian Xie, Kaari L. Linask et al. · Journal of Cardiovascular Disease Research Open access Oct 2011 56
48 High Sensitivity Scanning of Colorectal Tumors and Matched Plasma DNA for Mutations in APC, TP53, K‐RAS, and BRAF Genes with a Novel DHPLC Fluorescence Detection Platform Stan L. Lilleberg, Jeffrey A. Durocher, Charlotte Sanders et al. · Annals of the New York Academy of Sciences Jun 2004 56
49 Clinical and molecular study in congenital muscular dystrophy with partial laminin ?2 (LAMA2) deficiency Živana Težak, Paola Prandini, Marco Boscaro et al. · Human Mutation Open access 9 Jan 2003 55
50 Yield of the RYR2 Genetic Test in Suspected Catecholaminergic Polymorphic Ventricular Tachycardia and Implications for Test Interpretation Jamie D. Kapplinger, Krishna N. Pundi, Nicholas Bradley Larson et al. · Circulation Genomic and Precision Medicine Open access Feb 2018 52

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.