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Human chromosomes can have a few as 50 million base pairs to as many as 250 million base pairs.
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At DNA Genotek, we are proud of how our customers successfully use our products to achieve breakthroughs in genomic research. We would like to share their success with you and invite you to browse this section of our website to find out more about our enabling technology.
New Scientific Publications and Posters will be added to this site as they become available. Check back often for the latest material or email us to receive our quarterly newsletter.
If you notice that a relevant article is missing, please provide the reference so that it may be added by emailing us at marketing@dnagenotek.com |
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Acevedo, S. F. et al. Apolipoprotein E4 and sex affect neurobehavioral performance in primary school children. Pediatric Research 67(3): 293 – 299 (2010).
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Ambrosone, C. B. et al. Conducting Molecular Epidemiological Research in the Age of HIPAA: AMulti-Institutional Case-Control Study of Breast Cancer in African-American and European-AmericanWomen. Journal of Oncology 2009(871250): (2009).
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Asher, J. E. et al. A Whole-Genome Scan and Fine-Mapping Linkage Study of Auditory-Visual Synesthesia Reveals Evidence of Linkage to Chromosomes 2q24, 5q33, 6p12, and 12p12. The American Journal of Human Genetics 84: 279 – 285 (2009).
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Bar-Shira, A. et al. Ashkenazi Parkinson's disease patients with the LRRK2 G2019S mutation share a common founder dating from the second to fifth centuries. Neurogenetics 10: 355 – 358 (2009).
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Barcellos, L. F. et al. High-Density SNP Screening of the Major Histocompatibility Complex in Systemic Lupus Erythematosus Demonstrates Strong Evidence for Independent Susceptibility Regions. PLoS Genetics 5(10): 1 – 10 (2009).
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Basham, R. J. et al. Effect of HIV-1 Infection on Human DNA Yield from Saliva. HIV Clin Trials 10(4): 282 – 285 (2009).
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Becerik, S. et al. Exclusion of Candidate Genes in Seven Turkish Families with Autosomal Recessive Amelogenesis Imperfecta. Am J Med Genet Part A 149A:1392 – 1398 (2009).
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Bennett, R. R et al. Automated DNA mutation detection using universal conditions direct sequencing: application to ten muscular dystrophy genes. BMC Genetics: 10 – 66 (2009).
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Boles, R. G. Et al. Are pediatric and adult-onset cyclic vomiting syndrome (CVS) biologically different conditions? Relationship of adult-onset CVS with the migraine and pediatric CVSassociated common mtDNA polymorphisms 16519T and 3010A. Neurogastroenterol Motil 21: 936 – e72 (2009).
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Bossé, Y. et al. IdentiWcation of susceptibility genes for complex diseases using pooling-based genome-wide association scans. Hum Genet 125: 305 – 318 (2009).
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Brocke, B. et al. Stathmin, a Gene Regulating Neural Plasticity, Affects Fear and Anxiety Processing in Humans. Am J Med Genet Part B 153B: 243 – 251 (2009).
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Brocki K, et al., Assessing the Molecular Genetics of the Development of Executive Attention in Children: Focus on Genetic Pathways Related to the Anterior Cingulate Cortex and Dopamine. Neuroscience (2009).
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Brody, G. H. et al. Participation in a Family-Centered Prevention Program Decreases Genetic Risk for Adolescents' Risky Behaviors. Pediatrics 124: 911 – 917 (2009).
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Carroll, C. L. et al. ß2-Adrenergic Receptor Polymorphisms With Severe Asthma Exacerbations Affect Response to Treatment in Children. Chest 135: 1186 – 1192 (2009).
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Castano, R. et al. Evidence of association of interleukin-1 receptor-like 1 gene polymorphisms with chronic rhinosinusitis. American Journal of Rhinology & Allergy 23(4): 377 – 384 (2009).
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Chiang, P. W. et al. Somatic and Germ-Line Mosaicism in Rubinstein–Taybi Syndrome. Am J Med Genet Part A 149A:1463 – 1467 (2009).
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Chakkera, H.A. et al. Pilot Study: Association of Traditional and Genetic Risk Factors and New-Onset Diabetes Mellitus Following Kidney Transplantation. Transplantation Proceedings 41: 4172 – 4177 (2009).
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Greene, C. M. et al. Noradrenergic genotype predicts lapses in sustained attention. Neuropsychologia 47: 591 – 594 (2009).
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Corre, T. et al. A large-scale association study to assess the impact of known variants of the human INHA gene on premature ovarian failure. Human Reproduction 24(8): 2023 – 2028 (2009).
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Dick, D. M. et al. Role of GABRA2 in Trajectories of Externalizing Behavior Across Development and Evidence of Moderation by Parental Monitoring. Arch Gen Psychiatry 66(6): 649 – 657 (2009).
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Dickinson, J. L. et al. Past environmental sun exposure and risk of multiple sclerosis: a role for the Cdx-2 Vitamin D receptor variant in this interaction. Multiple Sclerosis 15: 563 – 570 (2009).
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Dieterich, K. et al. The Aurora Kinase C c.144delC mutation causes meiosis I arrest in men and is frequent in the North African population. Human Molecular Genetics 18(7): 1301 – 1309 (2009).
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Dillon, D. G. et al. Variation in TREK1 Gene Linked to Depression-Resistant Phenotype is Associated with Potentiated Neural Responses to Rewards in Humans. Human Brain Mapping: (2009).
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Dusatkova, P. et al. Association of IL23R p.381Gln and ATG16L1 p.197Ala With Crohn Disease in the Czech Population. Journal of Pediatric Gastroenterology and Nutrition 49: 405 – 410 (2009).
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El-Sayed, W. et al. Mutations in the Beta Propeller WDR72 Cause Autosomal-Recessive Hypomaturation Amelogenesis Imperfecta. The American Journal of Human Genetics 85: 699 – 705 (2009).
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Endam, L. M. et al. Polymorphisms in the interleukin-22 receptor alpha-1 gene are associated with severe chronic rhinosinusitis. Otolaryngology–Head and Neck Surgery 140: 741 – 747 (2009).
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Faruque, M. U. et al. Association of GNB3 C825T Polymorphism with Peak Oxygen Consumption. Association of GNB3 C825T …Int J Sports Med 30: 315 – 319 (2009).
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Frank, M. J. et al. Prefrontal and striatal dopaminergic genes predict individual differences in exploration and exploitation. Nature Neuroscience 12(8): 1062 – 1068 (2009).
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Frazier-Bowers, S. et al. Evidence of Linkage in a Hispanic Cohort with a Class III Dentofacial Phenotype. J Dent Res 88(1): 56 – 60 (2009).
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Gadji, M. et al. Is the 1p/19q deletion a diagnostic marker of oligodendrogliomas? Cancer Genetics and Cytogenetics 194: 12 – 22 (2009).
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Gurnett, C. A. et al. Genetic Linkage Localizes an Adolescent Idiopathic Scoliosis and Pectus Excavatum Gene to Chromosome 18 q. SPINE 34(2): E94 – E100 (2009).
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Grosjean, J. et al. Direct genotyping of cytomegalovirus envelope glycoproteins from toddler's saliva samples. J Clin Virol (2009).
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Harbuz, R. et al. Rôle d'aurora kinase C (AURKC) dans la reproduction humaine. Gynécologie Obstétrique & Fertilité 37: 546 – 551(2009).
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Isosomppi, J. et al. Disease-causing mutations in the CLRN1 gene alter normal CLRN1protein trafficking to the plasma membrane. Molecular Vision 15:1806 – 1818 (2009).
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Kim, H. S. et al. Culture, serotonin receptor polymorphism and locus of attention. The Author: (2009).
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Kolassa, I. et al. The Risk of Posttraumatic Stress Disorder After Trauma Depends on Traumatic Load and the Catechol-O-Methyltransferase Val158Met Polymorphism. Biol Psychiatry: (2009).
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Krynetskiy, E. et al. Introducing Pharmacy Students to Pharmacogenomic Analysis. American Journal of Pharmaceutical Education 73(4): (2009).
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Landa, I. et al. The Variant rs1867277 in FOXE1 Gene Confers Thyroid Cancer Susceptibility through the Recruitment of USF1/USF2 Transcription Factors. PLoS Genetics 5(9): (2009).
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Leger, P. et al. CYP2B6 Variants and Plasma Efavirenz Concentrations during Antiretroviral Therapy in Port-au-Prince, Haiti. J Infect Dis. 200(6): 955 – 964 (2009).
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Lim, K. S. et al. Determination of DNA Mutation Load in Human Tissues Using Denaturing HPLC-Based Heteroduplex Analysis. Methods Mol Biol 554: 287 – 299 (2009).
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Mackey, D. A. et al. Twins Eye Study in Tasmania (TEST): Rationale and Methodology to Recruit and Examine Twins. Twin Research and Human Genetics 12(5): 441 – 454 (2009).
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Madadi, P. et al. Pharmacogenetics of Neonatal Opioid Toxicity Following Maternal Use of Codeine During Breastfeeding: A Case–Control Study. Clinical pharmacology & Therapeutics 85(1): 31 – 35 (2009).
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Martinez, C. A. et al. Genetic association study of putative functional single nucleotide polymorphisms of genes in folate metabolism and spina bifida. Am J Obstet Gynecol 201:394.e1 – 394.e11 (2009).
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Medeiros-Domingo, A. et al. Comprehensive Open Reading Frame Mutational Analysis of the RYR2-Encoded Ryanodine Receptor/Calcium Channel in Patients Diagnosed Previously with Either Catecholaminergic Polymorphic Ventricular Tachycardia or Genotype Negative, Exercise-Induced Long QT Syndrome. J Am Coll Cardiol: 54(22): 2065 – 2074 (2009).
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Mitsouras, K. et al. Saliva as an alternative source of high yield canine genomic DNA for genotyping studies. BMC Research Note 2(219): (2009).
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Mohamed, J. A. et al. A Single-Nucleotide Polymorphism in the Gene Encoding Osteoprotegerin, an Anti-inflammatory Protein Produced in Response to Infection with Diarrheagenic Escherichia coli, Is Associated with an Increased Risk of Nonsecretory Bacterial Diarrhea in North American Travelers to Mexico. The Journal of Infectious Diseases 199: 477 – 485 (2009).
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Nishita, D. M. et al. Clinical trial participant characteristics and saliva and DNA metrics. BMC Medical Research Methodology 9(71): (2009).
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Nelson, S. S. et al. The genetics of colored sequence synesthesia: Evidence of linkage to chromosome 16q and genetic heterogeneity for the condition. Nature Precedings: (2009).
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Ollikka, P. et al. Genotyping of celiac disease-related-risk haplotypes using a closed-tube polymerase chain reaction analysis of dried blood and saliva disk samples. Analytical Biochemistry 386: 20 – 29 (2009).
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Racine, S. E. et al. The possible influence of impulsivity and dietary restraint on associations between serotonin genes and binge eating. Journal of Psychiatric Research 43: 1278 – 1286 (2009).
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Ribasés, M. et al. Case-Control Study of Six Genes Asymmetrically Expressed in the Two Cerebral Hemispheres: Association of BAIAP2 with Attention-Deficit/Hyperactivity Disorder. Biol Psychiatry: (2009).
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Rodrigues, S. M. et al. Oxytocin receptor genetic variation relates to empathy and stress reactivity in humans. PNAS Early Edition: (2009).
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Roe, B. E. et al. Risk-attitude selection bias in subject pools for experiments involving neuroimaging and blood samples. Journal of Economic Psychology 30: 181 – 189 (2009).
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Rylander-Rudqvist, T. et al. Quality and Quantity of Saliva DNA Obtained from the Self-administrated Oragene Method–A Pilot Study on the Cohort of Swedish Men. Cancer Epidemiol Biomarkers15 (9): 1742 – 1745 (2006).
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Santiago-Sim, T. et al. Sequencing of TGF-{beta} Pathway Genes in Familial Cases of Intracranial Aneurysm. Stroke; Journal of the American Heart Association 40: 1604 – 1611 (2009).
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Schacht, J. P. et al. Intermediate cannabis dependence phenotypes and the FAAH C385A variant: an exploratory analysis. Psychopharmacology 203: 511 – 517 (2009).
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Sjöholm, L. K. et al. PreproNPY Pro7 protects against depression despite exposure to environmental risk factors. Journal of Affective Disorders 118: 124 – 130 (2009).
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Szczepankiewicz, A. et al. Association of A/T polymorphism of the CHRM2 gene with bronchodilator response to ipratropium bromide in asthmatic children. Pneumonologia i Alergologia Polska 77(1): 5 – 10 (2009).
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Theusch, E. et al. Genome-wide Study of Families with Absolute Pitch Reveals Linkage to 8q24.21 and Locus Heterogeneity. The American Journal of Human Genetics 85: 112 – 119 (2009).
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Thomason, M. E. et al. BDNF genotype modulates resting functional connectivity in children. Frontiers in Human Neuroscience 3(55): 1 – 10 (2009).
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Tischfield, Max A. et al. Human TUBB3 Mutations Perturb Microtubule Dynamics, Kinesin Interactions, and Axon Guidance. Cell 140: 74 – 87 (2009).
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Toccaceli, V. et al. La Banca Biologica Del Registro Nazionale Gemelli. Not Ist Super Sanità 22(3): 3 – 7 (2009).
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Trynka, G. et al. Coeliac disease-associated risk variants in TNFAIP3 and REL implicate altered NF-KB signalling. Gut 58: 1078 – 1083 (2009).
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van de Kant, K. DG et al. Early diagnosis of asthma in young children by using non-invasive biomarkers of airway inflammation and early lung function measurements: study protocol of a case-control study. BMC Public Health 9(210): (2009).
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van der Zwaluw, C. S . et al. Interaction between dopamine D2 receptor genotype and parental rule-setting in adolescent alcohol use: evidence for a gene-parenting interaction. Molecular Psychiatry: 1 – 9 (2009).
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Viltrop, T. et al. Comparison of DNA extraction methods for multiplex PCR. Analytical Biochemistry: (2009).
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Vincent, A. L. et al. Exclusion of known corneal dystrophy genes in an autosomal dominant pedigree of a unique anterior membrane corneal dystrophy. Molecular Vision 15:1700 – 1708 (2009).
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Waugh, C. E. et al. Association Between the Catechol-O-Methyltransferase Val158Met Polymorphism and Self-Perceived Social Acceptance in Adolescent Girls. Journal of Child and Adolescent Psychopharmacology 19(4): 395 – 401 (2009).
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Wendland, J. R. et al. A Haplotype Containing Quantitative Trait Loci for SLC1A1 Gene Expression and Its Association with Obsessive-Compulsive Disorder. ARCH GEN PSYCHIATRY 66(4): 408 – 416 (2009).
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Wiener, H. W. Et al. Linkage analysis of schizophrenia in African-American families. Schizophrenia Research 109: 70 – 79 (2009).
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Wilson, M. L. et al. Maternal and fetal variants in the TGF-beta3 gene and risk of pregnancy-induced hypertension in a predominantly Latino population. Am J Obstet Gynecol 201: 295.e1 – 295.e5 (2009).
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Wright, J. T. et al. Phenotypic Variation in FAM83H-associated Amelogenesis Imperfecta. J Dent Res 88(4): 356 – 360 (2009).
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Zhang, L. et al. A Rapid and Reliable Test for BRCA1 and BRCA2 Founder Mutation Analysis in Paraffin Tissue Using Pyrosequencing. Journal of Molecular Diagnostics 11(3): 176 – 181 (2009).
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de Quervain, D.J. et al. A deletion variant of the alpha2b-adrenoceptor is related to emotional memory in Europeans and Africans. Nat Neurosci. 10(9): 1137-9 (2008).
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Graham, E.A.M. et al. Room temperature DNA preservation of soft tissue for rapid DNA extraction: an addition to the disaster victim identification investigators toolkit? Forensic Sciences Int Genetics 2(1): 29-34 (2008).
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Laios, E & Glynou K. et al. Allelic drop-out in the LDLR gene affects mutation detection in familial hypercholesterolemia. Clin Biochem. 41(1-2): 38-40 (2008).
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Gotlib, I. H. et al. HPA axis reactivity: A mechanism underlying the associations among 5-HTTLPR, stress, and depression. Bio Psychiatry 63(9): 847-51 (2008).
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Alexis, S. et al. Sexual Function in Women with Turner Syndrome. J Women's Health. 17(1): 27-33 (2008).
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Davidson, C. et al. Genes in Glucose Metabolism and Association w/ Spina Bifida. Reprod Sci. 15: 51-58 (2008).
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Burt, A. et al. Genes and Popularity: Evidence of an Evocative Gene-Environment Correlation. Psychol Sci. 19(2): 112-113 (2008).
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Everett, K. et al. Genome-wide High-Density SNP-Based Linkage Analysis of Infantile Hypertrophic Pyloric Stenosis Identifies Loci on Chromosomes 11q14-q22 and Xq23. Am J Hum Genet, 82(3): 756-762 (2008).
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Binder, E. B. et al. Association of FKBP5 Polymorphisms and Childhood Abuse with Risk of Posttraumatic Stress Disorder Symptoms in Adults. JAMA, 299(11): 1291-1305 (2008).
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Kimberling, J.W., et. al. Genetic Screening of Usher Syndrome in Children . ASHG abstract (2007).
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Hansen, T.V. et. al. Collection of blood, saliva, and buccal cell samples in a pilot study on the danish nurse cohort: comparison of the response rate and quality of genomic DNA. Cancer Epidemiol Biomarkers Prev. Oct;16(10):2072-6 (2007).
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Hannelius, U. et. al. Large-scale zygosity testing using single nucleotide polymorphisms. Twin Res Hum Genet. Aug;10(4):604-25 (2007).
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Cardy, J. O. el. al. Screening for dup7q11.23 in children with expressive language delay. Source: ASHG abstract (2007).
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Daksis,J.I. et. al. Heteropolymeric triplex-based genomic assay(r) to detect pathogens or single-nucleotide polymorphisms in human genomic samples. PLoS ONE, 2, e305. Notes: Ingeneus Research, Mississauga, Ontario, Canada (2007).
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de Quervain DJ, et. al. Nat Neurosci.A deletion variant of the alpha2b-adrenoceptor is related to emotional memory in Europeans and Africans.;10(9):1137-9. (2007).
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Duvefelt, K. el. al. Zygosity determination using DNA prepared from saliva. Karolinska University Hospital and Karolinska Insitutet. ASHG abstract (2007).
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Infante-Rivard,C., et. al. Excess Transmission of the NAD(P)H:Quinone Oxidoreductase 1 (NQO1) C609T Polymorphism in Families of Children with Acute Lymphoblastic Leukemia. Am. J. Epidemiol. 165(11):1248-54 (2007)
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Jin,Y., et. al. NALP1 in vitiligo-associated multiple autoimmune disease. N. Engl. J. Med., 356, 1216-1225. (2007).
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Ng, D.P., et. al. Saliva as a viable alternative source of human genomic DNA in genetic epidemiology. Clin. Chim. Acta, 367, 81-85 (2007).
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Robinson,W.P., et. al. Origin and outcome of pregnancies affected by androgenetic/biparental chimerism. Hum. Reprod., 22, 1114-1122 (2007).
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Rønningen,K.S., et. al. The Biobank of the Norwegian Mother and Child Cohort Study. Web site only. ISBER 2006 abstract (2007).
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Vitazka P. et. al. Saliva Suitable Specimen Alternative for DNA Genotyping Assays. AMP abstract (2007).
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Mishra B. K., et. al. Do motor control genes contribute to interindividual variability in decreased movement in patients with pain? Molecular Pain 3:20 doi:10.1186/1744-8069-3-20 (2007).
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Bellgrove et al. Dopaminergic genotype biases spatial attention in healthy children Mol Psych, 12, 786-792 (2007).
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Rogers,N.L., Cole,S., Lan,H.-C., Crossa,A., & Demerath,E.W. New saliva DNA collection method compared to buccal cell collection techniques for epidemiological studies. American Journal of Human Biology 19, 319-326 (2007).
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Amre, D.K. et al. Association between genetic variants in the IL-23R gene and early-onset Crohn's Disease: Results from a case-control and family-based study among Canadian Children. Am J Gastroenterol. 103(3): 615-20 (2007).
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Azmanov, D.N. et al. Persistence of the common Hartnup disease D173N allele in populations of European origin. Ann Hum Genet 71(6): 755-761 (2007).
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Berends, A. L. et al. STOX1 gene in pre-eclampsia and intrauterine growth restriction. BJOG 114(9): 1163-1167 (2007).
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Berteau-Pavy, F. et al. Effects of sex and APOE epsilon4 on object recognition and spatial navigation in the elderly. Neuroscience 147 (1): 6-17 (2007).
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Bondy, C. A. et al. The physical phenotype of girls and women with Turner syndrome is not X-imprinted. Hum Genet 121 (3-4): 469-474 (2007).
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Ester, A. R. et al. Apoptotic gene analyisis in idiopathic talipes equinovarus (clubfoot). Clin Orthop Relat Res 462: 32-37 (2007).
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Lachman, H. M. et al. Increase in GSK3beta gene copy number variation in bipolar disorder. Am. J. Med. Genet. B. Neuropsychiatr Genet. 144(3): 259-265 (2007).
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Lichtenstein, P. et al. The Swedish twin study of child and adolescent development: the TCHAD-study. Twin Res Hum Genet. 10(1): 67-73 (2007).
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Orr-Urtreger, A. et al. The LRRK2 G2019S mutation in Ashkenazi Jews with Parkinson disease: Is there a gender effect? Neurology 69(16): 1595-1602 (2007).
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Orr, A. et al. Mutations in the UBIAD1 gene, encoding a potential prenyltransferease, are causal for Schnyder cristalline corneal dystrophy. PLoS ONE 2(1):e685 (2007).
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Ellis, M. et al. Analysis of the 5q31–33 Locus Shows an Association between Single Nucleotide Polymorphism Variants in the IL-5 Gene and Symptomatic Infection with the Human Blood Fluke, Schistosoma japonicum. The Journal of Immuno. 179: 8366-8371 (2007).
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Pauline, L. et al. SLC40A1 c.1402GA Results in Aberrant Splicing, Ferroportin Truncation after Glycine 330, and an Autosomal Dominant Hemochromatosis Phenotype. Acta Haematol 118: 237-241 (2007).
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Stabley,D.L., et. al. Evaluation of STR-PCR and SNP-pyrosequencing for forensic and biomedical monitoring (2007).
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Ahituv, N., et. al. A PYY Q62P variant linked to human obesity. Hum. Mol. Genet. 15, 387-391 (2006).
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Evans,J.C., et. al. Germline mosaicism for a MECP2 mutation in a man with two Rett daughters. Clin. Genet., 70, 336-338 (2006).
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Lugassy, J., et al. Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis: two allelic ectodermal dysplasias caused by dominant mutations in KRT14. Am. J. Hum. Genet., 79, 724-730 (2006).
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Ng,D.P., Koh,D., Choo,S., & Chia,K.S. Saliva as a viable alternative source of human genomic DNA in genetic epidemiology. Clin. Chim. Acta 367, 81-85 (2006).
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Rylander-Rudqvist,T., Hakansson,N., Tybring,G., & Wolk,A. Quality and quantity of saliva DNA obtained from the self-administrated Oragene•DNA method--a pilot study on the cohort of Swedish men. Cancer Epidemiol. Biomarkers Prev. 15, 1742-1745 (2006).
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Self,J.E. et al. Fine mapping of the X-linked recessive congenital idiopathic nystagmus locus at Xq24-q26.3. Mol. Vis. 12, 1211-1216 (2006).
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Shaw,R.J., kufo-Tetteh,E.K., Risk,J.M., Field,J.K., & Liloglou,T. Methylation enrichment pyrosequencing: combining the specificity of MSP with validation by pyrosequencing. Nucleic Acids Res. 34, e78 (2006).
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Vastinsalo, H. et al. Two Finnish USH1B patients with three novel mutations in myosin VIIA. Mol Vis. 12: 1093-1097 (2006).
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McCready,M.E., et. al. A century later Farabee has his mutation. Hum. Genet., 117, 285-287 (2005).
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Weng,L., et. al. Lack of MEF2A mutations in coronary artery disease. J. Clin. Invest., 115, 1016-1020 (2005).
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