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Donald R. Love, Ph.D. - Publications

Affiliations: 
2014 Southeastern Baptist Theological Seminary 
Area:
Biblical Studies Religion, History of Religion
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0/238 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
Low-probability matches (unlikely to be authored by this person)
2024 Al-Maraghi A, Aamer W, Ziab M, Aliyev E, Elbashir N, Hussein S, Palaniswamy S, Anand D, Love DR, Charles A, A S Akil A, Fakhro KA. A loss-of-function AGTR1 variant in a critically-ill infant with renal tubular dysgenesis: case presentation and literature review. Bmc Nephrology. 25: 139. PMID 38649831 DOI: 10.1186/s12882-024-03569-z  0.01
2023 Mohammed I, Haris B, Al-Barazenji T, Vasudeva D, Tomei S, Al Azwani I, Dauleh H, Shehzad S, Chirayath S, Mohamadsalih G, Petrovski G, Khalifa A, Love DR, Al-Shafai M, Hussain K. Understanding the genetics of early onset obesity in a cohort of children from Qatar. The Journal of Clinical Endocrinology and Metabolism. PMID 37329217 DOI: 10.1210/clinem/dgad366  0.01
2023 Poquérusse J, Nolan M, Thorburn DR, Van Hove JLK, Friederich MW, Love DR, Taylor J, Powell CA, Minczuk M, Snell RG, Lehnert K, Glamuzina E, Jacobsen JC. Severe neonatal onset neuroregression with paroxysmal dystonia and apnoea: Expanding the phenotypic and genotypic spectrum of -related mitochondrial disease. Jimd Reports. 64: 223-232. PMID 37151360 DOI: 10.1002/jmd2.12360  0.01
2022 Glass GE, Mohammedali S, Sivakumar B, Stotland MA, Abdulkader F, Prosser DO, Love DR. Poland-Möbius syndrome: a case report implicating a novel mutation of the PLXND1 gene and literature review. Bmc Pediatrics. 22: 745. PMID 36581828 DOI: 10.1186/s12887-022-03803-3  0.01
2021 Theadom A, Rodrigues M, Ranta A, Poke G, Love D, Jones K, Ao BT, Hammond-Tooke G, Parmar P, O'Grady G, Roxburgh R. Impact and predictors of quality of life in adults diagnosed with a genetic muscle disorder: a nationwide population-based study. Quality of Life Research : An International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation. PMID 34837601 DOI: 10.1007/s11136-021-03046-2  0.01
2021 Guennoun A, Bougarn S, Khan T, Mackeh R, Rahman M, Al-Ali F, Ata M, Aamer W, Prosser D, Habib T, Chin-Smith E, Al-Darwish K, Zhang Q, Al-Shakaki A, Robay A, ... ... Love DR, et al. A Novel STK4 Mutation Impairs T Cell Immunity Through Dysregulation of Cytokine-Induced Adhesion and Chemotaxis Genes. Journal of Clinical Immunology. PMID 34427831 DOI: 10.1007/s10875-021-01115-2  0.01
2021 Acharya A, Kavus H, Dunn P, Nasir A, Folk L, Withrow K, Wentzensen IM, Ruzhnikov MRZ, Fallot C, Smol T, Rama M, Brown K, Whalen S, Ziegler A, Barth M, ... ... Love DR, et al. Delineating the genotypic and phenotypic spectrum of -related neurodevelopmental disorders. Journal of Medical Genetics. PMID 34321324 DOI: 10.1136/jmedgenet-2021-107871  0.01
2020 Casey T, Johnson C, Love D. Adult attention deficit hyperactivity disorder clinic: An interprofessional collaboration. Journal of the American Pharmacists Association : Japha. PMID 32616446 DOI: 10.1016/j.japh.2020.03.020  0.01
2020 Mohammed I, Al-Khawaga S, Bohanna D, Shabani A, Khan F, Love DR, Nawaz Z, Hussain K. Haploinsufficiency of the FOXA2 associated with a complex clinical phenotype. Molecular Genetics & Genomic Medicine. e1086. PMID 32277595 DOI: 10.1002/mgg3.1086  0.01
2020 Winbo A, Earle N, Marcondes L, Crawford J, Prosser DO, Love DR, Merriman TR, Cadzow M, Stiles R, Donoghue T, Stiles MK, Hayes I, Skinner JR. Genetic testing in Polynesian Long QT Syndrome probands reveals a lower diagnostic yield and an increased prevalence of rare variants. Heart Rhythm. PMID 32229296 DOI: 10.1016/j.hrthm.2020.03.015  0.01
2019 Brown A, Zamanpoor M, Love DR, Prosser DO. Determination of Pathogenicity of Gene Variants using the American College of Medical Genetics and Genomics and the Association for Molecular Pathology Guidelines. Sultan Qaboos University Medical Journal. 19: e324-e334. PMID 31897316 DOI: 10.18295/squmj.2019.19.04.008  0.01
2019 Lahrouchi N, Raju H, Lodder EM, Papatheodorou S, Miles C, Ware JS, Papadakis M, Tadros R, Cole D, Skinner JR, Crawford J, Love DR, Pua CJ, Soh BY, Bhalshankar JD, et al. The yield of postmortem genetic testing in sudden death cases with structural findings at autopsy. European Journal of Human Genetics : Ejhg. PMID 31534214 DOI: 10.1038/S41431-019-0500-8  0.01
2019 Raju H, Ware JS, Skinner JR, Hedley PL, Arno G, Love DR, van der Werf C, Tfelt-Hansen J, Winkel BG, Cohen MC, Li X, John S, Sharma S, Jeffery S, Wilde AAM, et al. Next-generation sequencing using microfluidic PCR enrichment for molecular autopsy. Bmc Cardiovascular Disorders. 19: 174. PMID 31337358 DOI: 10.1186/S12872-019-1154-8  0.01
2019 McKeage MJ, Tin Tin S, Khwaounjoo P, Sheath K, Dixon-McIver A, Ng D, Sullivan R, Cameron L, Shepherd P, Laking GR, Kingston N, Strauss M, Lewis C, Elwood M, Love DR. Screening for Anaplastic Lymphoma Kinase (ALK) gene rearrangements in non-small cell lung cancer (NSCLC) in New Zealand. Internal Medicine Journal. PMID 31318119 DOI: 10.1111/imj.14435  0.01
2019 Hughes P, Hassan I, Que L, Mead P, Lee JH, Love DR, Prosser DO, Cundy T. Observations on the Natural History of Camurati-Engelmann Disease. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. PMID 30690794 DOI: 10.1002/jbmr.3670  0.01
2019 Theadom A, Rodrigues M, Poke G, O'Grady G, Love D, Hammond-Tooke G, Parmar P, Baker R, Feigin V, Jones K, Te Ao B, Ranta A, Roxburgh R. A Nationwide, Population-Based Prevalence Study of Genetic Muscle Disorders. Neuroepidemiology. 52: 128-135. PMID 30661069 DOI: 10.1159/000494115  0.01
2018 Earle NJ, Crawford J, Hayes I, Rees MI, French J, Stiles MK, Waddell-Smith KE, Donoghue T, Monkley R, Neas K, Aitken A, Tse R, Love DR, Skinner JR. Development of a cardiac inherited disease service and clinical registry: A 15-year perspective. American Heart Journal. PMID 30686478 DOI: 10.1016/j.ahj.2018.11.013  0.01
2018 Gardner RJM, Crozier IG, Binfield AL, Love DR, Lehnert K, Gibson K, Lintott CJ, Snell RG, Jacobsen JC, Jones PP, Waddell-Smith KE, Kennedy MA, Skinner JR. Penetrance and expressivity of the R858H CACNA1C variant in a five-generation pedigree segregating an arrhythmogenic channelopathy. Molecular Genetics & Genomic Medicine. PMID 30345660 DOI: 10.1002/mgg3.476  0.01
2018 Jones KM, O'Grady G, Rodrigues MJ, Ranta A, Roxburgh RH, Love DR, Theadomon A. Impacts for Children Living with Genetic Muscle Disorders and their Parents - Findings from a Population-Based Study. Journal of Neuromuscular Diseases. PMID 30040738 DOI: 10.3233/JND-170287  0.01
2018 Marcondes L, Crawford J, Earle N, Smith W, Hayes I, Morrow P, Donoghue T, Graham A, Love D, Skinner JR. Long QT molecular autopsy in sudden unexplained death in the young (1-40 years old): Lessons learnt from an eight year experience in New Zealand. Plos One. 13: e0196078. PMID 29672598 DOI: 10.1371/Journal.Pone.0196078  0.01
2017 Shepherd P, Sheath KL, Tin ST, Khwaounjoo P, Aye PS, Li A, Laking GR, Kingston NJ, Lewis CA, Mark Elwood J, Love DR, McKeage MJ. Lung cancer mutation testing: a clinical retesting study of agreement between a real-time PCR and a mass spectrometry test. Oncotarget. 8: 101437-101451. PMID 29254176 DOI: 10.18632/oncotarget.21023  0.01
2017 Jacobsen JC, Whitford W, Swan B, Taylor J, Love DR, Hill R, Molyneux S, George PM, Mackay R, Robertson SP, Snell RG, Lehnert K. Compound Heterozygous Inheritance of Mutations in Coenzyme Q8A Results in Autosomal Recessive Cerebellar Ataxia and Coenzyme Q10 Deficiency in a Female Sib-Pair. Jimd Reports. PMID 29159460 DOI: 10.1007/8904_2017_73  0.01
2017 Leong IUS, Stuckey A, Belluoccio D, Fan V, Skinner JR, Prosser DO, Love DR. Massively Parallel Sequencing of Genes Implicated in Heritable Cardiac Disorders: A Strategy for a Small Diagnostic Laboratory. Medical Sciences (Basel, Switzerland). 5. PMID 29099038 DOI: 10.3390/medsci5040022  0.01
2017 Leong IUS, Dryland PA, Prosser DO, Lai SW, Graham M, Stiles M, Crawford J, Skinner JR, Love DR. Splice Site Variants in the KCNQ1 and SCN5A Genes: Transcript Analysis as a Tool in Supporting Pathogenicity. Journal of Clinical Medicine Research. 9: 709-718. PMID 28725320 DOI: 10.14740/jocmr2894w  0.01
2017 McKeage M, Elwood M, Tin Tin S, Khwaounjoo P, Aye P, Li A, Sheath K, Shepherd P, Laking G, Kingston N, Lewis C, Love D. EGFR Mutation Testing of non-squamous NSCLC: Impact and Uptake during Implementation of Testing Guidelines in a Population-Based Registry Cohort from Northern New Zealand. Targeted Oncology. PMID 28699084 DOI: 10.1007/s11523-017-0515-4  0.01
2017 Whitford W, Hawkins I, Glamuzina E, Wilson F, Marshall A, Ashton F, Love DR, Taylor J, Hill R, Lehnert K, Snell RG, Jacobsen JC. Compound heterozygous SLC19A3 mutations further refine the critical promoter region for biotin-thiamine-responsive basal ganglia disease. Cold Spring Harbor Molecular Case Studies. PMID 28696212 DOI: 10.1101/mcs.a001909  0.01
2017 Lahrouchi N, Raju H, Lodder EM, Papatheodorou E, Ware JS, Papadakis M, Tadros R, Cole D, Skinner JR, Crawford J, Love DR, Pua CJ, Soh BY, Bhalshankar JD, Govind R, et al. Utility of Post-Mortem Genetic Testing in Cases of Sudden Arrhythmic Death Syndrome. Journal of the American College of Cardiology. 69: 2134-2145. PMID 28449774 DOI: 10.1016/J.Jacc.2017.02.046  0.01
2017 Nickerson SL, Dryland PA, de Hora M, Love DR, Webster D. The development of a rapid molecular assay for severe combined immunodeficiency (SCID) using dried blood spots Pathology. 49: S31. DOI: 10.1016/J.PATHOL.2016.12.075  0.01
2016 Earle N, Crawford J, Gibson K, Love D, Hayes I, Neas K, Stiles M, Graham M, Donoghue T, Aitken A, Skinner J. Detection of sudden death syndromes in New Zealand. The New Zealand Medical Journal. 129: 67-74. PMID 27857240  0.01
2016 Nickerson SL, Prosser DO, Lai SW, Love DR. A comparison of benchtop high-throughput sequencing platforms in the diagnostic laboratory setting. Pathology. 48: S96. PMID 27773209 DOI: 10.1016/j.pathol.2015.12.271  0.01
2016 Nickerson SL, Lai SW, Tang R, Prosser DO, Love DR. A workflow for the detection and classification of variants in the BRCA1 and BRCA2 genes. Pathology. 48: S96. PMID 27773208 DOI: 10.1016/j.pathol.2015.12.272  0.01
2016 Nickerson SL, Marquis-Nicholson R, Claxton K, Ashton F, Leong IU, Prosser DO, Love JM, George AM, Taylor G, Wilson C, McKinlay Gardner RJ, Love DR. SNP analysis and whole exome sequencing: Their application in the analysis of a consanguineous pedigree segregating ataxia. Pathology. 48: S96-S97. PMID 27773207 DOI: 10.1016/j.pathol.2015.12.273  0.01
2016 Nickerson SL, Balasubramaniam S, Dryland PA, Love JM, Kava MP, Love DR, Prosser DO. Two Novel GLDC Mutations in a Neonate with Nonketotic Hyperglycinemia. Journal of Pediatric Genetics. 5: 174-80. PMID 27617160 DOI: 10.1055/s-0036-1584358  0.01
2016 Bagnall RD, Weintraub RG, Ingles J, Duflou J, Yeates L, Lam L, Davis AM, Thompson T, Connell V, Wallace J, Naylor C, Crawford J, Love DR, Hallam L, White J, et al. A Prospective Study of Sudden Cardiac Death among Children and Young Adults. The New England Journal of Medicine. 374: 2441-2452. PMID 27332903 DOI: 10.1056/NEJMoa1510687  0.01
2016 Tang R, Prosser DO, Love DR. Evaluation of Bioinformatic Programmes for the Analysis of Variants within Splice Site Consensus Regions. Advances in Bioinformatics. 2016: 5614058. PMID 27313609 DOI: 10.1155/2016/5614058  0.01
2016 Mc Cormack A, Claxton K, Ashton F, Asquith P, Atack E, Mazzaschi R, Moverley P, O'Connor R, Qorri M, Sheath K, Love DR, George AM. Microarray testing in clinical diagnosis: an analysis of 5,300 New Zealand patients. Molecular Cytogenetics. 9: 29. PMID 27034718 DOI: 10.1186/s13039-016-0237-9  0.01
2016 Ryder B, Knoll D, Love DR, Shepherd P, Love JM, Reed PW, de Hora M, Webster D, Glamuzina E, Wilson C. The natural history of elevated tetradecenoyl-L-carnitine detected by newborn screening in New Zealand: implications for very long chain acyl-CoA dehydrogenase deficiency screening and treatment. Journal of Inherited Metabolic Disease. PMID 26743058 DOI: 10.1007/s10545-015-9911-z  0.01
2016 Dryland P, Damhuis A, Rosendale D, Hughes K, Doherty E, Love D. Fragile X Syndrome Testing and the Limitations Associated with Current Maternal Cell Contamination Testing Strategies British Journal of Medicine and Medical Research. 17: 1-7. DOI: 10.9734/BJMMR/2016/28769  0.01
2016 McKeage M, Elwood J, Tin Tin S, Khwaounjoo P, Aye P, Li A, Shepherd P, Laking G, Kingston N, Lewis C, Love D. 455P Population-level impact of EGFR mutation testing in non-squamous NSCLC Annals of Oncology. 27. DOI: 10.1093/ANNONC/MDW594.019  0.01
2015 Nickerson SL, Marquis-Nicholson R, Claxton K, Ashton F, Leong IU, Prosser DO, Love JM, George AM, Taylor G, Wilson C, Gardner RJ, Love DR. SNP Analysis and Whole Exome Sequencing: Their Application in the Analysis of a Consanguineous Pedigree Segregating Ataxia. Microarrays (Basel, Switzerland). 4: 490-502. PMID 27600236 DOI: 10.3390/microarrays4040490  0.01
2015 Jacobsen JC, Glamuzina E, Taylor J, Swan B, Handisides S, Wilson C, Fietz M, van Dijk T, Appelhof B, Hill R, Marks R, Love DR, Robertson SP, Snell RG, Lehnert K. Whole Exome Sequencing Reveals Compound Heterozygosity for Ethnically Distinct PEX7 Mutations Responsible for Rhizomelic Chondrodysplasia Punctata, Type 1. Case Reports in Genetics. 2015: 454526. PMID 26587300 DOI: 10.1155/2015/454526  0.01
2015 Duffy L, Zhang L, Sheath K, Love DR, George AM. The Diagnosis of Choriocarcinoma in Molar Pregnancies: A Revised Approach in Clinical Testing. Journal of Clinical Medicine Research. 7: 961-966. PMID 26566410 DOI: 10.14740/jocmr2236w  0.01
2015 Jacobsen JC, Wilson C, Cunningham V, Glamuzina E, Prosser DO, Love DR, Burgess T, Taylor J, Swan B, Hill R, Robertson SP, Snell RG, Lehnert K. Brain dopamine-serotonin vesicular transport disease presenting as a severe infantile hypotonic parkinsonian disorder. Journal of Inherited Metabolic Disease. PMID 26497564 DOI: 10.1007/s10545-015-9897-6  0.01
2015 Earle N, Ingles J, Bagnall RD, Gray B, Crawford J, Smith W, Shelling AN, Love DR, Semsarian C, Skinner JR. NOS1AP Polymorphisms Modify QTc Interval Duration But Not Cardiac Arrest Risk in Hypertrophic Cardiomyopathy. Journal of Cardiovascular Electrophysiology. PMID 26332198 DOI: 10.1111/Jce.12827  0.01
2015 Mc Cormack A, Sharpe C, Gregersen N, Smith W, Hayes I, George AM, Love DR. 12q14 Microdeletions: Additional Case Series with Confirmation of a Macrocephaly Region. Case Reports in Genetics. 2015: 192071. PMID 26266063 DOI: 10.1155/2015/192071  0.01
2015 Turner C, Mein R, Sharpe C, Love DR. Merosin-deficient congenital muscular dystrophy: A novel homozygous mutation in the laminin-2 gene. Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia. 22: 1983-5. PMID 26249246 DOI: 10.1016/j.jocn.2015.04.016  0.01
2015 Brookes C, Lai S, Doherty E, Love DR. Predicting the Pathogenic Potential of BRCA1 and BRCA2 Gene Variants Identified in Clinical Genetic Testing. Sultan Qaboos University Medical Journal. 15: e218-25. PMID 26052455  0.01
2015 Leong IU, Stuckey A, Lai D, Skinner JR, Love DR. Assessment of the predictive accuracy of five in silico prediction tools, alone or in combination, and two metaservers to classify long QT syndrome gene mutations. Bmc Medical Genetics. 16: 34. PMID 25967940 DOI: 10.1186/s12881-015-0176-z  0.01
2015 Leong IU, Sucich J, Prosser DO, Skinner JR, Crawford JR, Higgins C, Love DR. Array comparative genomic hybridization identifies a heterozygous deletion of exon 3 of the RYR2 gene. Upsala Journal of Medical Sciences. 1-8. PMID 25835811 DOI: 10.3109/03009734.2015.1029101  0.01
2015 Earle NJ, Poppe KK, Pilbrow AP, Cameron VA, Troughton RW, Skinner JR, Love DR, Shelling AN, Whalley GA, Ellis CJ, Richards AM, Doughty RN. Genetic markers of repolarization and arrhythmic events after acute coronary syndromes. American Heart Journal. 169: 579-86.e3. PMID 25819866 DOI: 10.1016/j.ahj.2014.11.015  0.01
2015 Lai S, Brookes C, Prosser DO, Lan CC, Doherty E, Love DR. Diagnostic Screening Workflow for Mutations in the BRCA1 and BRCA2 Genes. Sultan Qaboos University Medical Journal. 15: e58-70. PMID 25685387  0.01
2015 Rodrigues M, Kidd A, Love DR, Roxburgh R. The New Zealand Neuromuscular Disease Registry: rate of diagnoses confirmed by molecular testing. Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia. 22: 434-6. PMID 25443090 DOI: 10.1016/j.jocn.2014.06.096  0.01
2015 Wu TY, Willoughby E, Hutchinson DO, Brew S, McGuinness B, Lopes R, Love DR, Roxburgh RH. Congestive myeloradiculopathy in a patient with Cowden syndrome. Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia. 22: 431-3. PMID 25304432 DOI: 10.1016/j.jocn.2014.07.023  0.01
2015 Dryland P, Hughes K, Han D, Aziz A, Zhu D, Doherty E, Love D. Myotonic Dystrophy: Accurately Scoring the Boundaries that Define Regions of Triplet Repeat Expansion Mutations British Journal of Medicine and Medical Research. 8: 724-731. DOI: 10.9734/BJMMR/2015/18303  0.01
2015 Lai SW, Lopes RM, Doherty E, Prosser DO, Tang R, Love DR. Analysis of BRCA gene missense mutations Journal of Biomedical Engineering and Informatics. 2: 91. DOI: 10.5430/JBEI.V2N1P91  0.01
2014 Mazzaschi RL, Taylor J, Robertson SP, Love DR, George AM. A turner syndrome patient carrying a mosaic distal x chromosome marker. Case Reports in Genetics. 2014: 597314. PMID 24778889 DOI: 10.1155/2014/597314  0.01
2014 Te Weehi L, Maikoo R, Mc Cormack A, Mazzaschi R, Ashton F, Zhang L, George AM, Love DR. Microduplication of 3p26.3 implicated in cognitive development. Case Reports in Genetics. 2014: 295359. PMID 24778888 DOI: 10.1155/2014/295359  0.01
2014 Skinner JR, Marquis-Nicholson R, Luangpraseuth A, Cutfield R, Crawford J, Love DR. Diabetic Dead-in-Bed Syndrome: A Possible Link to a Cardiac Ion Channelopathy. Case Reports in Medicine. 2014: 647252. PMID 24715918 DOI: 10.1155/2014/647252  0.01
2014 Mc Cormack A, Taylor J, Te Weehi L, Love DR, George AM. A case of 17q21.31 microduplication and 7q31.33 microdeletion, associated with developmental delay, microcephaly, and mild dysmorphic features. Case Reports in Genetics. 2014: 658570. PMID 24649381 DOI: 10.1155/2014/658570  0.01
2014 Glengarry JM, Crawford J, Morrow PL, Stables SR, Love DR, Skinner JR. Long QT molecular autopsy in sudden infant death syndrome. Archives of Disease in Childhood. 99: 635-40. PMID 24596401 DOI: 10.1136/archdischild-2013-305331  0.01
2014 Marquis-Nicholson R, Prosser DO, Love JM, Zhang L, Hayes I, George AM, Crawford JR, Skinner JR, Love DR. Array comparative genomic hybridization identifies a heterozygous deletion of the entire KCNJ2 gene as a cause of sudden cardiac death. Circulation. Cardiovascular Genetics. 7: 17-22. PMID 24395924 DOI: 10.1161/CIRCGENETICS.113.000415  0.01
2014 Skinner JR, Love DR. The left and right atria finally express themselves. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 11: 272-3. PMID 24239843 DOI: 10.1016/j.hrthm.2013.11.010  0.01
2014 Earle N, Yeo Han D, Pilbrow A, Crawford J, Smith W, Shelling AN, Cameron V, Love DR, Skinner JR. Single nucleotide polymorphisms in arrhythmia genes modify the risk of cardiac events and sudden death in long QT syndrome. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 11: 76-82. PMID 24096169 DOI: 10.1016/J.Hrthm.2013.10.005  0.01
2014 Love JM, Prosser D, Love DR, Chintakindi KP, Dalal AB, Aggarwal S. A novel glycine decarboxylase gene mutation in an Indian family with nonketotic hyperglycinemia. Journal of Child Neurology. 29: 122-7. PMID 23349517 DOI: 10.1177/0883073812471432  0.01
2014 Leong I, Skinner J, Love D. Application of Massively Parallel Sequencing in the Clinical Diagnostic Testing of Inherited Cardiac Conditions Medical Sciences. 2: 98-126. DOI: 10.3390/MEDSCI2020098  0.01
2014 Marcondes L, Crawford J, Earle N, Smith W, Donoghue T, Love D, Graham M, Morrow P, Skinner J. Long QT gene testing in autopsy-negative sudden death in the young: Influence of age and gender on diagnostic yield Heart Lung and Circulation. 23. DOI: 10.1016/J.Hlc.2014.07.035  0.01
2014 Earle N, Smith W, Crawford J, Love D, Hayes I, Graham M, Donoghue T, Hood M, Stiles M, Skinner J. The prevalence of emerging genotypic risk factors in patients with long QT syndrome Heart Lung and Circulation. 23. DOI: 10.1016/J.Hlc.2014.07.024  0.01
2014 Earle N, Poppe K, Cameron V, Pilbrow A, Troughton R, Skinner J, Love D, Shelling A, Richards M, Doughty R. Risk of sudden cardiac death following acute coronary syndromes: Interplay of single nucleotide polymorphisms and the presence of heart failure Heart, Lung and Circulation. 23: e9. DOI: 10.1016/J.HLC.2014.07.023  0.01
2014 Skinner J, Crawford J, Waddell-Smith K, Earle N, Donoghue T, Graham M, Hayes I, Stiles M, Smith W, Love D. Development of the New Zealand cardiac inherited disease registry Heart Lung and Circulation. 23. DOI: 10.1016/J.Hlc.2014.07.010  0.01
2013 Marquis-Nicholson R, Prosser D, Love JM, Love DR. Gene Dosage Analysis in a Clinical Environment: Gene-Targeted Microarrays as the Platform-of-Choice. Microarrays (Basel, Switzerland). 2: 51-62. PMID 27605180 DOI: 10.3390/microarrays2020051  0.01
2013 Leong IU, Skinner JR, Shelling AN, Love DR. Expression of a Mutant kcnj2 Gene Transcript in Zebrafish. Isrn Molecular Biology. 2013: 324839. PMID 27335675 DOI: 10.1155/2013/324839  0.01
2013 Dryland PA, Doherty E, Love JM, Love DR. Simple Repeat-Primed PCR Analysis of the Myotonic Dystrophy Type 1 Gene in a Clinical Diagnostics Environment. Journal of Neurodegenerative Diseases. 2013: 857564. PMID 26317000 DOI: 10.1155/2013/857564  0.01
2013 Wheeler BJ, Patterson N, Love DR, Prosser D, Tomlinson P, Taylor BJ, Manning P. Frequency and genetic spectrum of maturity-onset diabetes of the young (MODY) in southern New Zealand. Journal of Diabetes and Metabolic Disorders. 12: 46. PMID 24355479 DOI: 10.1186/2251-6581-12-46  0.01
2013 Brookes C, Prosser DO, Love JM, Gardner RJ, Love DR. Diagnostic genetics at a distance: von hippel-lindau disease and a novel mutation. Genetics Research International. 2013: 189196. PMID 24062953 DOI: 10.1155/2013/189196  0.01
2013 Sheath KL, Mazzaschi RL, Aftimos S, Gregersen NE, George AM, Love DR. Clinical Outcomes and Counselling Issues regarding Partial Trisomy of Terminal Xp in a Child with Developmental Delay. Sultan Qaboos University Medical Journal. 13: 311-7. PMID 23862040  0.01
2013 Mazzaschi RL, Ashton F, Aftimos S, George AM, Love DR. Implications of a Chr7q21.11 Microdeletion and the Role of the PCLO Gene in Developmental Delay. Sultan Qaboos University Medical Journal. 13: 306-10. PMID 23862039  0.01
2013 Mc Cormack A, Taylor J, Gregersen N, George AM, Love DR. Delineation of 2q32q35 deletion phenotypes: two apparent "proximal" and "distal" syndromes. Case Reports in Genetics. 2013: 823451. PMID 23840981 DOI: 10.1155/2013/823451  0.01
2013 Sheath KL, Duffy L, Asquith P, Love DR, George AM. Bacterial artificial chromosomes (BACs)-on-Beadsâ„¢ as a diagnostic platform for the rapid aneuploidy screening of products of conception. Molecular Medicine Reports. 8: 650-4. PMID 23764829 DOI: 10.3892/mmr.2013.1519  0.01
2013 Marquis-Nicholson R, Aftimos S, Love DR. Molecular Analysis of a Case of Thanatophoric Dysplasia Reveals Two de novo FGFR3 Missense Mutations located in cis. Sultan Qaboos University Medical Journal. 13: 80-7. PMID 23573386  0.01
2013 Marquis-Nicholson R, Doherty E, Love JM, Lan CC, George AM, Thrush A, Love DR. Array-based Identification of Copy Number Changes in a Diagnostic Setting: Simultaneous gene-focused and low resolution whole human genome analysis. Sultan Qaboos University Medical Journal. 13: 69-79. PMID 23573385  0.01
2013 Elston MS, Meyer-Rochow GY, Prosser D, Love DR, Conaglen JV. Novel mutation in the TMEM127 gene associated with phaeochromocytoma. Internal Medicine Journal. 43: 449-51. PMID 23551308 DOI: 10.1111/imj.12088  0.01
2013 Doherty E, O'Connor R, Zhang A, Lim C, Love JM, Ashton F, Claxton K, Gregersen N, George AM, Love DR. Developmental delay referrals and the roles of Fragile X testing and molecular karyotyping: a New Zealand perspective. Molecular Medicine Reports. 7: 1710-4. PMID 23525284 DOI: 10.3892/mmr.2013.1386  0.01
2013 Marquis-Nicholson R, Lai D, Lan CC, Love JM, Love DR. A Streamlined Protocol for Molecular Testing of the DMD Gene within a Diagnostic Laboratory: A Combination of Array Comparative Genomic Hybridization and Bidirectional Sequence Analysis. Isrn Neurology. 2013: 908317. PMID 23476807 DOI: 10.1155/2013/908317  0.01
2013 Boudry-Labis E, Demeer B, Le Caignec C, Isidor B, Mathieu-Dramard M, Plessis G, George AM, Taylor J, Aftimos S, Wiemer-Kruel A, Kohlhase J, Annerén G, Firth H, Simonic I, Vermeesch J, ... ... Love DR, et al. A novel microdeletion syndrome at 9q21.13 characterised by mental retardation, speech delay, epilepsy and characteristic facial features. European Journal of Medical Genetics. 56: 163-70. PMID 23279911 DOI: 10.1016/j.ejmg.2012.12.006  0.01
2013 Roxburgh RH, Marquis-Nicholson R, Ashton F, George AM, Lea RA, Eccles D, Mossman S, Bird T, van Gassen KL, Kamsteeg EJ, Love DR. The p.Ala510Val mutation in the SPG7 (paraplegin) gene is the most common mutation causing adult onset neurogenetic disease in patients of British ancestry. Journal of Neurology. 260: 1286-94. PMID 23269439 DOI: 10.1007/S00415-012-6792-Z  0.01
2013 Earle N, Crawford J, Smith W, Hayes I, Shelling A, Hood M, Stiles M, Maxwell F, Heaven D, Love DR, Skinner JR. Community detection of long QT syndrome with a clinical registry: an alternative to ECG screening programs? Heart Rhythm : the Official Journal of the Heart Rhythm Society. 10: 233-8. PMID 23123674 DOI: 10.1016/J.Hrthm.2012.10.043  0.01
2013 McKeage MJ, Shepherd P, Yozu M, Love DR. Tumour mutation profiling with high-throughput multiplexed genotyping: A review of its use for guiding targeted cancer therapy Current Cancer Therapy Reviews. 9: 236-244. DOI: 10.2174/157339470904140418093822  0.01
2013 Patterson N, Taylor B, Dainty G, Prosser D, Tomlinson P, Love D, Wheeler B. Spectrum of MODY in the south of New Zealand – including two novel mutations International Journal of Pediatric Endocrinology. 2013. DOI: 10.1186/1687-9856-2013-S1-P39  0.01
2013 Marquis-Nicholson R, Roxburgh RH, Ashton F, Love DR. The p.Ala510Val variant in the SPG7 gene: re-assessing the pathogenic significance of a ‘benign’ polymorphism Pathology. 45: S30. DOI: 10.1097/01.PAT.0000426796.02505.17  0.01
2012 Lan CC, Love DR. Molecular Characterisation of Bacterial Community Structure along the Intestinal Tract of Zebrafish (Danio rerio): A Pilot Study. Isrn Microbiology. 2012: 590385. PMID 23724326 DOI: 10.5402/2012/590385  0.01
2012 Singh S, Ashton F, Marquis-Nicholson R, Love JM, Lan CC, Aftimos S, George AM, Love DR. A novel 2.3 mb microduplication of 9q34.3 inserted into 19q13.4 in a patient with learning disabilities. Case Reports in Pediatrics. 2012: 459602. PMID 23198235 DOI: 10.1155/2012/459602  0.01
2012 Sims K, Mazzaschi RL, Payne E, Hayes I, Love DR, George AM. A rare chromosome 3 imbalance and its clinical implications. Case Reports in Pediatrics. 2012: 846564. PMID 23097735 DOI: 10.1155/2012/846564  0.01
2012 Al-Murrani A, Ashton F, Aftimos S, George AM, Love DR. Amino-Terminal Microdeletion within the CNTNAP2 Gene Associated with Variable Expressivity of Speech Delay. Case Reports in Genetics. 2012: 172408. PMID 23074684 DOI: 10.1155/2012/172408  0.01
2012 George AM, Taylor J, Love DR. Microdeletions in 16p11.2 and 13q31.3 associated with developmental delay and generalized overgrowth. Genetics and Molecular Research : Gmr. 11: 3133-7. PMID 23007991 DOI: 10.4238/2012.September.3.1  0.01
2012 Rodrigues M, Hammond-Tooke G, Kidd A, Love D, Patel R, Dawkins H, Bellgard M, Roxburgh R. The New Zealand Neuromuscular Disease Registry. Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia. 19: 1749-50. PMID 22999565 DOI: 10.1016/j.jocn.2012.04.008  0.01
2012 Lai D, Love DR. Automation of a primer design and evaluation pipeline for subsequent sequencing of the coding regions of all human Refseq genes. Bioinformation. 8: 365-8. PMID 22570517 DOI: 10.6026/97320630008365  0.01
2012 Leong IU, Lan CC, Skinner JR, Shelling AN, Love DR. In vivo testing of microRNA-mediated gene knockdown in zebrafish. Journal of Biomedicine & Biotechnology. 2012: 350352. PMID 22500088 DOI: 10.1155/2012/350352  0.01
2012 Lan CC, Blake D, Henry S, Love DR. Fluorescent function-spacer-lipid construct labelling allows for real-time in vivo imaging of cell migration and behaviour in zebrafish (Danio rerio). Journal of Fluorescence. 22: 1055-63. PMID 22434405 DOI: 10.1007/s10895-012-1043-3  0.01
2012 Lai D, Lan CC, Leong IU, Love DR. Zebrafish dystrophin and utrophin genes: dissecting transcriptional expression during embryonic development. International Journal of Molecular Medicine. 29: 338-48. PMID 22200618 DOI: 10.3892/ijmm.2011.865  0.01
2012 Edmunds SJ, Roy NC, Davy M, Cooney JM, Barnett MP, Zhu S, Park Z, Love DR, Laing WA. Effects of kiwifruit extracts on colonic gene and protein expression levels in IL-10 gene-deficient mice. The British Journal of Nutrition. 108: 113-29. PMID 22152591 DOI: 10.1017/S0007114511005241  0.01
2012 Jain R, von Hurst PR, Stonehouse W, Love DR, Higgins CM, Coad J. Association of vitamin D receptor gene polymorphisms with insulin resistance and response to vitamin D. Metabolism: Clinical and Experimental. 61: 293-301. PMID 21871642 DOI: 10.1016/j.metabol.2011.06.018  0.01
2012 Webb SE, Cheung CC, Chan CM, Love DR, Miller AL. Application of complementary luminescent and fluorescent imaging techniques to visualize nuclear and cytoplasmic Ca²⁺ signalling during the in vivo differentiation of slow muscle cells in zebrafish embryos under normal and dystrophic conditions. Clinical and Experimental Pharmacology & Physiology. 39: 78-86. PMID 21824171 DOI: 10.1111/j.1440-1681.2011.05582.x  0.01
2012 George AM, Love DR, Hayes I, Tsang B. Recurrent transmission of a 17q12 microdeletion and a variable clinical spectrum Molecular Syndromology. 2: 72-75. DOI: 10.1159/000335344  0.01
2012 Roxburgh RH, Marquis-Nicholson R, Hutchinson DO, Waddell LB, Clarke NF, North KN, Love DR. G.P.46 Screening for deletion and duplication mutations in genes implicated in LGMD Neuromuscular Disorders. 22: 833. DOI: 10.1016/J.Nmd.2012.06.105  0.01
2011 O'Connor R, Al-Murrani A, Aftimos S, Asquith P, Mazzaschi R, Eyrolle-Guignot D, George AM, Love DR. Pure duplication of the distal long arm of chromosome 15 with ebstein anomaly and clavicular anomaly. Case Reports in Genetics. 2011: 898706. PMID 23074681 DOI: 10.1155/2011/898706  0.01
2011 Mazzaschi RL, Love DR, Hayes I, George A. Inheritance of a Ring Chromosome 21 in a Couple Undergoing In Vitro Fertilization (IVF): A Case Report. Case Reports in Genetics. 2011: 158086. PMID 23074672 DOI: 10.1155/2011/158086  0.01
2011 Johnson RA, Hellens RP, Love DR. A transient assay for recombination demonstrates that Arabidopsis SNM1 and XRCC3 enhance non-homologous recombination. Genetics and Molecular Research : Gmr. 10: 2104-32. PMID 21968679 DOI: 10.4238/vol10-3gmr1347  0.01
2011 Lan CC, Leong IUS, Lai D, Love DR. Disease Modeling by Gene Targeting Using MicroRNAs Methods in Cell Biology. 105: 419-436. PMID 21951541 DOI: 10.1016/B978-0-12-381320-6.00018-7  0.01
2011 Leong IU, Lai D, Lan CC, Johnson R, Love DR, Johnson R, Love DR. Targeted mutagenesis of zebrafish: use of zinc finger nucleases. Birth Defects Research. Part C, Embryo Today : Reviews. 93: 249-55. PMID 21932433 DOI: 10.1002/bdrc.20213  0.01
2011 Singh S, Aftimos S, George A, Love DR. Interstitial deletion of 10q23.1 and confirmation of three 10qdel syndromes Singapore Medical Journal. 52. PMID 21808946  0.01
2011 Marquis-Nicholson R, Aftimos S, Ashton F, Love JM, Stone P, McFarlane J, George AM, Love DR. Pseudotrisomy 13 syndrome: use of homozygosity mapping to target candidate genes. Gene. 486: 37-40. PMID 21756987 DOI: 10.1016/j.gene.2011.06.028  0.01
2011 George A, Marquis-Nicholson R, Zhang LT, Love JM, Ashton F, Aftimos S, Hayes I, Williams LC, Love DR. Chromosome microarray analysis in a clinical environment: New perspective and new challenge British Journal of Biomedical Science. 68: 100-108. PMID 21706924 DOI: 10.1080/09674845.2011.11730334  0.01
2011 Edmunds SJ, Roy NC, Love DR, Laing WA. Kiwifruit extracts inhibit cytokine production by lipopolysaccharide-activated macrophages, and intestinal epithelial cells isolated from IL10 gene deficient mice. Cellular Immunology. 270: 70-9. PMID 21600571 DOI: 10.1016/j.cellimm.2011.04.004  0.01
2011 Cheung CY, Webb SE, Love DR, Miller AL. Visualization, characterization and modulation of calcium signaling during the development of slow muscle cells in intact zebrafish embryos. The International Journal of Developmental Biology. 55: 153-74. PMID 21553383 DOI: 10.1387/ijdb.103160cc  0.01
2011 Kim DD, Croxson MS, Cranshaw IM, Evans JL, Marquis-Nicholson R, Love DR. Indolent medullary thyroid cancer with a RET proto-oncogene Cys618Phe mutation presenting as sporadic unilateral pheochromocytoma in a 55-year-old Korean woman. Thyroid : Official Journal of the American Thyroid Association. 21: 325-6. PMID 21254918 DOI: 10.1089/thy.2010.0310  0.01
2011 Glamuzina E, Marquis-Nicholson R, Knoll D, Love DR, Wilson C. Citrullinaemia type I: a common mutation in the Pacific Island population. Journal of Paediatrics and Child Health. 47: 262-5. PMID 21244552 DOI: 10.1111/j.1440-1754.2010.01948.x  0.01
2011 Rice KS, Dickson G, Lane M, Crawford J, Chung SK, Rees MI, Shelling AN, Love DR, Skinner JR. Elevated serum gastrin levels in Jervell and Lange-Nielsen syndrome: a marker of severe KCNQ1 dysfunction? Heart Rhythm : the Official Journal of the Heart Rhythm Society. 8: 551-4. PMID 21118729 DOI: 10.1016/j.hrthm.2010.11.039  0.01
2011 Skinner JR, Crawford J, Smith W, Aitken A, Heaven D, Evans CA, Hayes I, Neas KR, Stables S, Koelmeyer T, Denmark L, Vuletic J, Maxwell F, White K, Yang T, ... ... Love DR, et al. Prospective, population-based long QT molecular autopsy study of postmortem negative sudden death in 1 to 40 year olds. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 8: 412-9. PMID 21070882 DOI: 10.1016/J.Hrthm.2010.11.016  0.01
2011 East EW, Love DR. Value-added analysis of the construction submittal process Automation in Construction. 20: 1070-1078. DOI: 10.1016/j.autcon.2011.04.008  0.01
2010 Ashton F, O'Connor R, Love JM, Doherty E, Aftimos S, George A, Love DR. Molecular characterisation of a der(Y)t(Xp;Yp) with Xp functional disomy and sex reversal Genetics and Molecular Research : Gmr. 9: 1815-1823. PMID 20845307 DOI: 10.4238/vol9-3gmr896  0.01
2010 Marquis-Nicholson R, Glamuzina E, Prosser D, Wilson C, Love DR. Citrullinemia type I: molecular screening of the ASS1 gene by exonic sequencing and targeted mutation analysis Genetics and Molecular Research : Gmr. 9: 1483-1489. PMID 20690080 DOI: 10.4238/vol9-3gmr834  0.01
2010 Marquis-Nicholson R, Aftimos S, Hayes I, George A, Love DR. Array comparative genomic hybridisation: a new tool in the diagnostic genetic armoury. The New Zealand Medical Journal. 123: 50-61. PMID 20651866  0.01
2010 Ameratunga R, Woon ST, Neas K, Love DR. The clinical utility of molecular diagnostic testing for primary immune deficiency disorders: a case based review. Allergy, Asthma, and Clinical Immunology : Official Journal of the Canadian Society of Allergy and Clinical Immunology. 6: 12. PMID 20529312 DOI: 10.1186/1710-1492-6-12  0.01
2010 Leong IU, Skinner JR, Shelling AN, Love DR. Identification and expression analysis of kcnh2 genes in the zebrafish. Biochemical and Biophysical Research Communications. 396: 817-24. PMID 20438705 DOI: 10.1016/j.bbrc.2010.04.157  0.01
2010 Leong IUS, Skinner JR, Shelling AN, Love DR. Zebrafish as a model for long QT syndrome: The evidence and the means of manipulating zebrafish gene expression Acta Physiologica. 199: 257-276. PMID 20331541 DOI: 10.1111/j.1748-1716.2010.02111.x  0.01
2010 Gladding PA, Evans CA, Crawford J, Chung SK, Vaughan A, Webster D, Neas K, Love DR, Rees MI, Shelling AN, Skinner JR. Posthumous diagnosis of long QT syndrome from neonatal screening cards. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 7: 481-6. PMID 20167303 DOI: 10.1016/j.hrthm.2009.12.023  0.01
2010 Skinner JR, Love DR. The SCN5A gene in Brugada syndrome: mutations, variants, missense and nonsense. What's a clinician to do? Heart Rhythm : the Official Journal of the Heart Rhythm Society. 7: 50-1. PMID 20129285 DOI: 10.1016/j.hrthm.2009.10.019  0.01
2010 Andresen JH, Aftimos S, Doherty E, Love DR, Battin M. 13q33.2 deletion: A rare cause of ambiguous genitalia in a male newborn with growth restriction Acta Paediatrica, International Journal of Paediatrics. 99: 784-786. PMID 20105145 DOI: 10.1111/j.1651-2227.2010.01683.x  0.01
2010 Aftimos S, Asquith P, Ashton F, Vasilevski O, Love DR. Distal 5q deletion with associated parietal foramina. Clinical Dysmorphology. 19: 43-7. PMID 19952731 DOI: 10.1097/MCD.0b013e3283345596  0.01
2010 Ferguson LR, Baker PI, Love DR. Application of Nutrigenomics in Gastrointestinal Health Genomics, Proteomics, and Metabolomics in Nutraceuticals and Functional Foods. 83-94. DOI: 10.1002/9780813821474.ch8  0.01
2009 Lan CC, Tang R, Un San Leong I, Love DR. Quantitative real-time RT-PCR (qRT-PCR) of zebrafish transcripts: optimization of RNA extraction, quality control considerations, and data analysis. Cold Spring Harbor Protocols. 2009: pdb.prot5314. PMID 20147059 DOI: 10.1101/pdb.prot5314  0.01
2009 Baker PI, Love DR, Ferguson LR. Role of gut microbiota in Crohn's disease. Expert Review of Gastroenterology & Hepatology. 3: 535-46. PMID 19817674 DOI: 10.1586/egh.09.47  0.01
2009 Khadilkar SV, Singh RK, Hegde M, Urtizberea A, Love DR, Chong B. Spectrum of mutations in sarcoglycan genes in the Mumbai region of western India: high prevalence of 525del T. Neurology India. 57: 406-10. PMID 19770540 DOI: 10.4103/0028-3886.55603  0.01
2009 Ramachandran A, Marshall ES, Love DR, Baguley BC, Shelling AN. Activin is a potent growth suppressor of epithelial ovarian cancer cells. Cancer Letters. 285: 157-65. PMID 19493612 DOI: 10.1016/j.canlet.2009.05.010  0.01
2009 Tan TY, Aftimos S, Worgan L, Susman R, Wilson M, Ghedia S, Kirk EP, Love D, Ronan A, Darmanian A, Slavotinek A, Hogue J, Moeschler JB, Ozmore J, Widmer R, et al. Phenotypic expansion and further characterisation of the 17q21.31 microdeletion syndrome. Journal of Medical Genetics. 46: 480-9. PMID 19447831 DOI: 10.1136/jmg.2008.065391  0.01
2009 Skinner J, Crawford J, Vaughan A, Gladding P, Eddy C, Love D, Rees M, Shelling A. Posthumous Diagnosis of Long QT Syndrome from the Neonatal Screening Card Heart, Lung and Circulation. 18: S82. DOI: 10.1016/J.HLC.2009.05.183  0.01
2009 Wu E, Al-Murrani A, Doherty E, Aftimos S, George A, Love DR. Chimerism detected in fraternal twins using ABI AmpFlSTR® Identifiler Forensic Science International: Genetics Supplement Series. 2: 226-227. DOI: 10.1016/j.fsigss.2009.08.144  0.01
2008 Eddy CA, MacCormick JM, Chung SK, Crawford JR, Love DR, Rees MI, Skinner JR, Shelling AN. Identification of large gene deletions and duplications in KCNQ1 and KCNH2 in patients with long QT syndrome. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 5: 1275-81. PMID 18774102 DOI: 10.1016/j.hrthm.2008.05.033  0.01
2008 Ramachandran A, Black MA, Shelling AN, Love DR. Microarrays--analysis of signaling pathways. Methods in Molecular Medicine. 141: 115-30. PMID 18453087  0.01
2008 Dryland PA, Love DR, Walker MF, Dommels Y, Butts C, Rowan D, Roy NC, Helsby N, Browning BL, Zhu S, Copp BR, Ferguson LR. Allantoin as A Biomarker of Inflammation in an Inflammatory Bowel Disease Mouse Model: NMR Analysis of Urine The Open Bioactive Compounds Journal. 1: 1-6. DOI: 10.2174/1874847300801010001  0.01
2008 Stapleton PM, Lai D, Millar CD, Wu E, Andres M, Love DR. Discovery of three related females who type XY at the amelogenin locus Forensic Science International: Genetics Supplement Series. 1: 577-579. DOI: 10.1016/j.fsigss.2007.08.017  0.01
2007 Lan CC, Laurenson S, Copp BR, Cattin PM, Love DR. Whole organism approaches to chemical genomics: the promising role of zebrafish (Danio rerio). Expert Opinion On Drug Discovery. 2: 1389-401. PMID 23484534 DOI: 10.1517/17460441.2.10.1389  0.01
2007 Tang R, Dodd A, Lai D, McNabb WC, Love DR. Validation of zebrafish (Danio rerio) reference genes for quantitative real-time RT-PCR normalization. Acta Biochimica Et Biophysica Sinica. 39: 384-90. PMID 17492136 DOI: 10.1111/j.1745-7270.2007.00283.x  0.01
2007 Love DR, Lan CC, Dodd A, Shelling AN, McNabb WC, Ferguson LR. Modeling inflammatory bowel disease: the zebrafish as a way forward. Expert Review of Molecular Diagnostics. 7: 177-93. PMID 17331065 DOI: 10.1586/14737159.7.2.177  0.01
2006 Dodd A, Greenwood DR, Miller AL, Webb SE, Chambers SP, Copp BR, Love DR. Zebrafish: at the nexus of functional and chemical genomics. Biotechnology & Genetic Engineering Reviews. 22: 77-99. PMID 18476327 DOI: 10.1080/02648725.2006.10648066  0.01
2004 Pichler FB, Dodd A, Love DR. Global gene expression analysis in the zebrafish: the challenge and the promise. Drug Discovery Today. Technologies. 1: 79-84. PMID 24981375 DOI: 10.1016/j.ddtec.2004.06.005  0.01
2004 Pichler FB, Black MA, Williams LC, Love DR. Design, Normalization, and Analysis of Spotted Microarray Data Methods in Cell Biology. 77: 521-543. PMID 15602930 DOI: 10.1016/S0091-679X(04)77028-4  0.01
2004 Dodd A, Chambers SP, Nielsen PE, Love DR. Modeling human disease by gene targeting. Methods in Cell Biology. 76: 593-612. PMID 15602894 DOI: 10.1016/S0091-679X(04)76027-6  0.01
2004 Love DR, Pichler FB, Dodd A, Copp BR, Greenwood DR. Technology for high-throughput screens: the present and future using zebrafish. Current Opinion in Biotechnology. 15: 564-71. PMID 15560983 DOI: 10.1016/J.Copbio.2004.09.004  0.01
2004 Hedge MR, Wu F, Chong B, Chin ELH, Hutchinson DO, Richards CS, Khadilkar S, Love DR. Limb girdle muscular dystrophy: Use of dHPLC and direct sequencing to detect sarcoglycan gene mutations in a New Zealand cohort [2] Clinical Genetics. 65: 55-60. PMID 15032976 DOI: 10.1111/J.2004.00193.X  0.01
2004 Dodd A, Chambers SP, Love DR. Short interfering RNA-mediated gene targeting in the zebrafish. Febs Letters. 561: 89-93. PMID 15013756 DOI: 10.1016/S0014-5793(04)00129-2  0.01
2003 Chong B, Hegde M, Fawkner M, Simonet S, Cassinelli H, Coker M, Kanis J, Seidel J, Tau C, Tüysüz B, Yüksel B, Love D. Idiopathic hyperphosphatasia and TNFRSF11B mutations: relationships between phenotype and genotype. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 18: 2095-104. PMID 14672344 DOI: 10.1359/jbmr.2003.18.12.2095  0.01
2003 Pichler FB, Laurenson S, Williams LC, Dodd A, Copp BR, Love DR. Chemical discovery and global gene expression analysis in zebrafish. Nature Biotechnology. 21: 879-83. PMID 12894204 DOI: 10.1038/Nbt852  0.01
2003 Chambers SP, Anderson LV, Maguire GM, Dodd A, Love DR. Sarcoglycans of the zebrafish: orthology and localization to the sarcolemma and myosepta of muscle. Biochemical and Biophysical Research Communications. 303: 488-95. PMID 12659844 DOI: 10.1016/S0006-291X(03)00355-3  0.01
2003 West PM, Love DR, Stapleton PM, Winship IM. Paternal uniparental disomy in monozygotic twins discordant for hemihypertrophy. Journal of Medical Genetics. 40: 223-6. PMID 12624145 DOI: 10.1136/jmg.40.3.223  0.01
2002 Cundy T, Hegde M, Naot D, Chong B, King A, Wallace R, Mulley J, Love DR, Seidel J, Fawkner M, Banovic T, Callon KE, Grey AB, Reid IR, Middleton-Hardie CA, et al. A mutation in the gene TNFRSF11B encoding osteoprotegerin causes an idiopathic hyperphosphatasia phenotype. Human Molecular Genetics. 11: 2119-27. PMID 12189164 DOI: 10.1093/Hmg/11.18.2119  0.01
2002 Wong J, Love DR, Kyle C, Daniels A, White M, Stewart AW, Schnell AH, Elston RC, Holdaway IM, Mountjoy KG. Melanocortin-3 receptor gene variants in a Maori kindred with obesity and early onset type 2 diabetes. Diabetes Research and Clinical Practice. 58: 61-71. PMID 12161058 DOI: 10.1016/S0168-8227(02)00126-2  0.01
2001 Wu G, Richards CS, Wu W, Hegde M, Fawkner M, Chong B, Love D, Su LK, Lynch P, Snow K. Detection of sequence variations in the adenomatous polyposis coli (APC) gene using denaturing high-performance liquid chromatography Genetic Testing. 5: 281-290. PMID 11960572 DOI: 10.1089/109065701753617408  0.01
2001 Hedge MR, Chong B, Stevenson C, Laing NG, Khadilkar S, Love DR. Clinical & genetic analysis of four patients with distal upper limb spinal muscular atrophy Indian Journal of Medical Research. 114: 141-147. PMID 11921836  0.01
2001 Hegde MR, Chong B, Fawkner M, Lambiris N, Peters H, Kenneson A, Warren ST, Love DR, McGaughran J. Microdeletion in the FMR-1 gene: An apparent null allele using routine clinical PCR amplification [5] Journal of Medical Genetics. 38: 624-629. PMID 11565550 DOI: 10.1136/Jmg.38.9.624  0.01
2001 Hegde MR, Fawkner M, Chong B, McGaughran J, Gilbert D, Love DR. Compound heterozygosity at the FMR1 gene Genetic Testing. 5: 135-138. PMID 11551100 DOI: 10.1089/109065701753145600  0.01
2001 Francis-Thickpenny KM, Richardson DM, van Ee CC, Love DR, Winship IM, Baguley BC, Chenevix-Trench G, Shelling AN. Analysis of the TGF beta functional pathway in epithelial ovarian carcinoma. British Journal of Cancer. 85: 687-91. PMID 11531253 DOI: 10.1054/bjoc.2001.1950  0.01
2001 Chambers SP, Dodd A, Overall R, Sirey T, Lam LT, Morris GE, Love DR. Dystrophin in adult zebrafish muscle Biochemical and Biophysical Research Communications. 286: 478-483. PMID 11511083 DOI: 10.1006/Bbrc.2001.5424  0.01
2001 Roeder AD, Marshall RK, Mitchelson AJ, Visagathilagar T, Ritchie PA, Love DR, Pakai TJ, McPartlan HC, Murray ND, Robinson NA, Kerry KR, Lambert DM. Gene flow on the ice: genetic differentiation among Adélie penguin colonies around Antarctica. Molecular Ecology. 10: 1645-56. PMID 11472533 DOI: 10.1046/j.0962-1083.2001.01312.x  0.01
2001 Shelling AN, Burton KA, Chand AL, van Ee CC, France JT, Farquhar CM, Milsom SR, Love DR, Gersak K, Aittomäki K, Winship IM. Inhibin: A Candidate Gene for Premature Ovarian Failure Obstetric and Gynecologic Survey. 56: 279-280. DOI: 10.1097/00006254-200105000-00019  0.01
2000 Shelling AN, Burton KA, Chand AL, van Ee CC, France JT, Farquhar CM, Milsom SR, Love DR, Gersak K, Aittomäki K, Winship IM. Inhibin: a candidate gene for premature ovarian failure. Human Reproduction (Oxford, England). 15: 2644-9. PMID 11098038 DOI: 10.1093/HUMREP/15.12.2644  0.01
2000 Hegde MR, Chong B, Fawkner MJ, Leary J, Shelling AN, Culling B, Winship I, Love DR. Hierarchical mutation screening protocol for the BRCA1 gene. Human Mutation. 16: 422-30. PMID 11058900 DOI: 10.1002/1098-1004(200011)16:5<422::AID-HUMU7>3.0.CO;2-3  0.01
2000 Dodd A, Curtis PM, Williams LC, Love DR. Zebrafish: Bridging the gap between development and disease Human Molecular Genetics. 9: 2443-2449. PMID 11005800 DOI: 10.1093/HMG/9.16.2443  0.01
2000 Williams LC, Hegde MR, Nagappan R, Faull RL, Giles J, Winship I, Snow K, Love DR. Null alleles at the Huntington disease locus: implications for diagnostics and CAG repeat instability. Genetic Testing. 4: 55-60. PMID 10794362 DOI: 10.1089/109065700316480  0.01
2000 Clements L, Manilal S, Love DR, Morris GE. Direct interaction between emerin and lamin A Biochemical and Biophysical Research Communications. 267: 709-714. PMID 10673356 DOI: 10.1006/bbrc.1999.2023  0.01
1999 Williams LC, Hedge MR, Herrera G, Stapleton PM, Love DR. Comparative semi-automated analysis of (CAG) repeats in the Huntington disease gene: Use of internal standards Molecular and Cellular Probes. 13: 283-289. PMID 10441201 DOI: 10.1006/mcpr.1999.0248  0.01
1999 Manilal S, Sewry CA, Pereboev A, Thi Man N, Gobbi P, Hawkes S, Love DR, Morris GE. Distribution of emerin and lamins in the heart and implications for Emery-Dreifuss muscular dystrophy Human Molecular Genetics. 8: 353-359. PMID 9949197 DOI: 10.1093/hmg/8.2.353  0.01
1998 Butterworth NJ, Williams L, Bullock JY, Love DR, Faull RL, Dragunow M. Trinucleotide (CAG) repeat length is positively correlated with the degree of DNA fragmentation in Huntington's disease striatum. Neuroscience. 87: 49-53. PMID 9722140 DOI: 10.1016/S0306-4522(98)00129-8  0.01
1998 Czuchwicki A, Plummer JL, Love DR, Owen H, Ilsley AH. Influence of premedication with diazepam or morphine on the induction dose of eltanolone Acta Anaesthesiologica Scandinavica. 42: 527-531. PMID 9605367  0.01
1997 Dodd A, Rowland SA, Hawkes SLJ, Kennedy MA, Love DR. Mutations in the adrenoleukodystrophy gene Human Mutation. 9: 500-511. PMID 9195223 DOI: 10.1002/(SICI)1098-1004(1997)9:6<500::AID-HUMU2>3.0.CO;2-5  0.01
1996 Passos-Bueno MR, Moreira ES, Marie SK, Bashir R, Vasquez L, Love DR, Vainzof M, Iughetti P, Oliveira JR, Bakker E, Strachan T, Bushby K, Zatz M. Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 Brazilian families. Journal of Medical Genetics. 33: 97-102. PMID 8929943 DOI: 10.1136/jmg.33.2.97  0.01
1996 Love DR, Owen H, Ilsley AH, Plummer JL, Hawkins RM, Morrison A. A comparison of variable-dose patient-controlled analgesia with fixed- dose patient-controlled analgesia Anesthesia and Analgesia. 83: 1060-1064. PMID 8895286 DOI: 10.1097/00000539-199611000-00028  0.01
1996 Kennedy MA, Rowland SA, Miller AL, Morris CM, Neville LA, Dodd A, Fifield WJ, Love DR. Structure and location of the murine adrenoleukodystrophy gene Genomics. 32: 395-400. PMID 8838803 DOI: 10.1006/geno.1996.0134  0.01
1996 Rowland SA, Dodd A, Roche AL, Manilal S, Kennedy MA, Becroft DMO, Tonkin S, Chapman C, Love DR. DNA-based diagnostics for adrenoleukodystrophy in a large New Zealand family New Zealand Medical Journal. 109: 312-315. PMID 8816721  0.01
1996 Norris PJ, Waldvogel HJ, Faull RL, Love DR, Emson PC. Decreased neuronal nitric oxide synthase messenger RNA and somatostatin messenger RNA in the striatum of Huntington's disease. Neuroscience. 72: 1037-47. PMID 8735228 DOI: 10.1016/0306-4522(95)00596-X  0.01
1996 Augood SJ, Faull RL, Love DR, Emson PC. Reduction in enkephalin and substance P messenger RNA in the striatum of early grade Huntington's disease: a detailed cellular in situ hybridization study. Neuroscience. 72: 1023-36. PMID 8735227 DOI: 10.1016/0306-4522(95)00595-1  0.01
1996 Whitefield JE, Williams L, Snow K, Dixon J, Winship I, Stapleton PM, Faull RM, Love DR. Molecular analysis of the Huntington's disease gene in New Zealand. The New Zealand Medical Journal. 109: 27-30. PMID 8606810  0.01
1995 King SC, Roche AL, Passos-Bueno MR, Takata R, Zatz M, Cockburn DJ, Seller A, Stapleton PM, Love DR. Molecular characterization of further dystrophin gene microsatellites. Molecular and Cellular Probes. 9: 361-70. PMID 8569778 DOI: 10.1016/S0890-8508(95)91700-4  0.01
1995 Laing NG, Wilton SD, Akkari PA, Dorosz S, Boundy K, Kneebone C, Blumbergs P, White S, Watkins H, Love DR. A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy. Nature Genetics. 9: 75-9. PMID 7704029 DOI: 10.1038/ng0195-75  0.01
1994 King SC, Stapleton PM, Walker AP, Love DR. Two dinucleotide repeat polymorphisms at the DMD locus Human Molecular Genetics. 3: 523. PMID 8012374 DOI: 10.1093/hmg/3.3.523  0.01
1994 Tunnacliffe A, Jackson MS, Gardner E, Love DR, Moore JK, Mole SE, Mulligan LM, Graham A, Finocchiaro G, Orstavik S. A multiple interval physical map of the pericentromeric region of human chromosome 10. Human Genetics. 93: 313-8. PMID 7907314 DOI: 10.1007/BF00212029  0.01
1993 Love DR, Gardner E, Ponder BAJ. A polymorphic dinucleotide repeat at the D10S141 locus Human Molecular Genetics. 2: 491. PMID 8504318 DOI: 10.1093/hmg/2.4.491  0.01
1993 Love DR, Byth BC, Tinsley JM, Blake DJ, Davies KE. Dystrophin and dystrophin-related proteins: a review of protein and RNA studies. Neuromuscular Disorders : Nmd. 3: 5-21. PMID 8329888 DOI: 10.1016/0960-8966(93)90037-K  0.01
1993 Le TT, Nguyen TM, Love DR, Helliwell TR, Davies KE, Morris GE. Monoclonal antibodies against the muscle-specific N-terminus of dystrophin: characterization of dystrophin in a muscular dystrophy patient with a frameshift deletion of exons 3-7. American Journal of Human Genetics. 53: 131-9. PMID 8317478  0.01
1993 Mulligan LM, Kwok JB, Healey CS, Elsdon MJ, Eng C, Gardner E, Love DR, Mole SE, Moore JK, Papi L. Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A. Nature. 363: 458-60. PMID 8099202 DOI: 10.1038/363458A0  0.01
1993 Gardner E, Papi L, Easton DF, Cummings T, Jackson CE, Kaplan M, Love DR, Mole SE, Moore JK, Mulligan LM. Genetic linkage studies map the multiple endocrine neoplasia type 2 loci to a small interval on chromosome 10q11.2. Human Molecular Genetics. 2: 241-6. PMID 8098977 DOI: 10.1093/Hmg/2.3.241  0.01
1993 Love D, Gardner E, Ponder B. A polymorphic dinucleotide repeat at the ZNF22 locus Human Molecular Genetics. 2: 491-491. DOI: 10.1093/HMG/2.4.491-A  0.01
1992 Dunckley MG, Love DR, Davies KE, Walsh FS, Morris GE, Dickson G. Retroviral-mediated transfer of a dystrophin minigene into mdx mouse myoblasts in vitro. Febs Letters. 296: 128-34. PMID 1733767 DOI: 10.1016/0014-5793(92)80363-L  0.01
1992 Tinsley JM, Blake DJ, Roche A, Fairbrother U, Riss J, Byth BC, Knight AE, Kendrick-Jones J, Suthers GK, Love DR. Primary structure of dystrophin-related protein. Nature. 360: 591-3. PMID 1461283 DOI: 10.1038/360591A0  0.01
1992 Byth BC, Love DR, Murray JC, Davies KE. Localization of two new DNA markers on the linkage map of human chromosome 6q. Cytogenetics and Cell Genetics. 60: 216-8. PMID 1354595 DOI: 10.1159/000133342  0.01
1992 Walker AP, Chelly J, Love DR, Brush YI, Récan D, Chaussain JL, Oley CA, Connor JM, Yates J, Price DA, Super M, Bottani A, Steinman B, Kaplan JC, Davies KE, et al. A YAC contig in Xp21 containing the adrenal hypoplasia congenita and glycerol kinase deficiency genes Human Molecular Genetics. 1: 579-585. PMID 1301166 DOI: 10.1093/Hmg/1.8.579  0.01
1992 Blake DJ, Love DR, Tinsley J, Morris GE, Turley H, Gatter K, Dickson G, Edwards YH, Davies KE. Characterization of a 4.8kb transcript from the Duchenne muscular dystrophy locus expressed in Schwannoma cells. Human Molecular Genetics. 1: 103-9. PMID 1301145 DOI: 10.1093/hmg/1.2.103  0.01
1992 Wells DJ, Wells KE, Walsh FS, Davies KE, Goldspink G, Love DR, Chan-Thomas P, Dunckley MG, Piper T, Dickson G. Human dystrophin expression corrects the myopathic phenotype in transgenic mdx mice. Human Molecular Genetics. 1: 35-40. PMID 1301134 DOI: 10.1093/Hmg/1.1.35  0.01
1992 Habets GGM, Kammen RAvd, Serikawa T, Yamada J, Kubota S, Nakai Y, Kuro-o M, Kohno S, Sola L, Rossi A, Iaselli V, Rasch E, Monaco P, Rossi AR, Rasch EM, ... ... Love DR, et al. Subject Index Vol. 60, 1992 Cytogenetic and Genome Research. 60: 276-276. DOI: 10.1159/000133357  0.01
1992 Love DR, Hunter MN. Expansions in series of legendre functions Proceedings of the London Mathematical Society. 579-601. DOI: 10.1112/plms/s3-64.3.579  0.01
1991 Love DR, England SB, Speer A, Marsden RF, Bloomfield JF, Roche AL, Cross GS, Mountford RC, Smith TJ, Davies KE. Sequences of junction fragments in the deletion-prone region of the dystrophin gene. Genomics. 10: 57-67. PMID 2045110 DOI: 10.1016/0888-7543(91)90484-V  0.01
1991 Luthi E, Bhana Jasmat N, Grayling RA, Love DR, Bergquist PL. Cloning, sequence analysis, and expression in Escherichia coli of a gene coding for a β-mannanase from the extremely thermophilic bacterium 'Caldocellum saccharolyticum' Applied and Environmental Microbiology. 57: 694-700. PMID 2039230 DOI: 10.1128/aem.57.3.694-700.1991  0.01
1991 Love DR, Morris GE, Ellis JM, Fairbrother U, Marsden RF, Bloomfield JF, Edwards YH, Slater CP, Parry DJ, Davies KE. Tissue distribution of the dystrophin-related gene product and expression in the mdx and dy mouse. Proceedings of the National Academy of Sciences of the United States of America. 88: 3243-7. PMID 2014247 DOI: 10.1073/Pnas.88.8.3243  0.01
1991 Passos-Bueno MR, Terwilliger J, Ott J, Vainzof M, Love DR, Davies KE, Zatz M. Linkage analysis in families with autosomal recessive limb-girdle muscular dystrophy (LGMD) and 6q probes flanking the dystrophin-related sequence. American Journal of Medical Genetics. 38: 140-6. PMID 2012126 DOI: 10.1002/Ajmg.1320380130  0.01
1991 Dickson G, Love DR, Davies KE, Wells KE, Piper TA, Walsh FS. Human dystrophin gene transfer: production and expression of a functional recombinant DNA-based gene. Human Genetics. 88: 53-8. PMID 1959926 DOI: 10.1007/Bf00204929  0.01
1991 Passos-Bueno MR, Byth B, Love D, Terwilliger J, Ott J, Rapaport D, Vainzof M, Zatz M, Davies KE. Exclusion of the gene responsible for facioscapulohumeral muscular dystrophy (FSH) at 6q23-q27. Journal of the Neurological Sciences. 102: 206-8. PMID 1883411 DOI: 10.1016/0022-510X(91)90070-N  0.01
1991 Acsadi G, Dickson G, Love DR, Jani A, Walsh FS, Gurusinghe A, Wolff JA, Davies KE. Human dystrophin expression in mdx mice after intramuscular injection of DNA constructs. Nature. 352: 815-8. PMID 1881437 DOI: 10.1038/352815A0  0.01
1991 Rapaport D, Passos-Bueno MR, Brandão L, Love D, Vainzof M, Zatz M. Apparent association of mental retardation and specific patterns of deletions screened with probes cf56a and cf23a in Duchenne muscular dystrophy. American Journal of Medical Genetics. 39: 437-41. PMID 1877622 DOI: 10.1002/ajmg.1320390414  0.01
1991 Love DR, Flint TJ, Genet SA, Middleton-Price HR, Davies KE. Becker muscular dystrophy patient with a large intragenic dystrophin deletion: implications for functional minigenes and gene therapy. Journal of Medical Genetics. 28: 860-4. PMID 1757963 DOI: 10.1136/Jmg.28.12.860  0.01
1991 Nguyen TM, Ellis JM, Love DR, Davies KE, Gatter KC, Dickson G, Morris GE. Localization of the DMDL gene-encoded dystrophin-related protein using a panel of nineteen monoclonal antibodies: presence at neuromuscular junctions, in the sarcolemma of dystrophic skeletal muscle, in vascular and other smooth muscles, and in proliferating brain cell lines. The Journal of Cell Biology. 115: 1695-700. PMID 1757469 DOI: 10.1083/Jcb.115.6.1695  0.01
1991 Byth BC, Love DR, Passos-Bueno MR, Davies KE. A new DNA marker, D6S129, identifies a HindIII polymorphism on chromosome 6q. Nucleic Acids Research. 19: 4310. PMID 1678512 DOI: 10.1093/nar/19.15.4310-a  0.01
1990 England SB, Nicholson LVB, Johnson MA, Forrest SM, Love DR, Zubrzycka-Gaarn EE, Bulman DE, Harris JB, Davies KE. Very mild muscular dystrophy associated with the deletion of 46% of dystrophin Nature. 343: 180-182. PMID 2404210 DOI: 10.1038/343180A0  0.01
1990 Love DR, Flint TJ, Marsden RF, Bloomfield JF, Daniels RJ, Forrest SM, Gabrielli O, Giorgi P, Novelli G, Davies KE. Characterization of deletions in the dystrophin gene giving mild phenotypes American Journal of Medical Genetics. 37: 136-142. PMID 2240031 DOI: 10.1002/ajmg.1320370132  0.01
1990 Buckle VJ, Guenet JL, Simon-Chazottes D, Love DR, Davies KE. Localisation of a dystrophin-related autosomal gene to 6q24 in man, and to mouse chromosome 10 in the region of the dystrophia muscularis (dy) locus Human Genetics. 85: 324-326. PMID 2203673 DOI: 10.1007/BF00206755  0.01
1990 Passos-Bueno MR, Rapaport D, Love D, Flint T, Bortolini ER, Zatz M, Davies KE. Screening of deletions in the dystrophin gene with the cDNA probes Cf23a, Cf56a, and Cf115. Journal of Medical Genetics. 27: 145-50. PMID 2182872 DOI: 10.1136/jmg.27.3.145  0.01
1990 Saul DJ, Williams LC, Grayling RA, Chamley LW, Love DR, Bergquist PL. celB, a gene coding for a bifunctional cellulase from the extreme thermophile 'Caldocellum saccharolyticum' Applied and Environmental Microbiology. 56: 3117-3124. PMID 2126700 DOI: 10.1128/aem.56.10.3117-3124.1990  0.01
1990 Luthi E, Love DR, McAnulty J, Wallace C, Caughey PA, Saul D, Bergquist PL. Cloning, sequence analysis, and expression of genes encoding Xylan-degrading enzymes from the thermophile 'Caldocellum saccharolyticum' Applied and Environmental Microbiology. 56: 1017-1024. PMID 2111111 DOI: 10.1128/AEM.56.4.1017-1024.1990  0.01
1990 Love DR, Bloomfield JF, Kenwrick SJ, Yates JRW, Davies KE. Physical mapping distal to the DMD locus Genomics. 8: 106-112. PMID 2081587 DOI: 10.1016/0888-7543(90)90231-I  0.01
1990 Man Nt, Cartwright AJ, Morris GE, Love DR, Bloomfield JF, Davies KE. Monoclonal antibodies against defined regions of the muscular dystrophy protein, dystrophin Febs Letters. 262: 237-240. PMID 1692289 DOI: 10.1016/0014-5793(90)80199-S  0.01
1989 Saul DJ, Williams LC, Love DR, Chamley LW, Bergquist PL. Nucleotide sequence of a gene from Caldocellum saccharolyticum encoding for exocellulase and endocellulase activity Nucleic Acids Research. 17: 439. PMID 2789517 DOI: 10.1093/nar/17.1.439  0.01
1989 Speer A, Rosenthal A, Billwitz H, Hanke R, Forrest SM, Love D, Davies KE, Coutelle C. DNA amplification of a further exon of Duchenne muscular dystrophy locus increase possibilities for deletion screening. Nucleic Acids Research. 17: 4892. PMID 2783234 DOI: 10.1093/nar/17.12.4892  0.01
1989 Love DR, Forrest SM, Smith TJ, England S, Flint T, Davies KE, Speer A. Molecular analysis of duschenne and becker muscular dystrophies British Medical Bulletin. 45: 659-680. PMID 2688822 DOI: 10.1093/OXFORDJOURNALS.BMB.A072351  0.01
1989 Love DR, Davies KE. Duchenne muscular dystrophy: The gene and the protein Molecular Biology and Medicine. 6: 7-17. PMID 2666821  0.01
1989 Love DR, Hill DF, Dickson G, Spurr NK, Byth BC, Marsden RF, Walsh FS, Edwards YH, Davies KE. An autosomal transcript in skeletal muscle with homology to dystrophin. Nature. 339: 55-8. PMID 2541343 DOI: 10.1038/339055A0  0.01
1989 Speer A, Rosenthal A, Billwitz H, Hanke R, Forrest S, Love D, Davies K, Love D. DNA amplification of a further eion of Duchenne mnscular dystrophy locus increase possibilities for deletion screening Nucleic Acids Research. 17: 6774-6774. DOI: 10.1093/nar/17.16.6774-a  0.01
1988 Dickson G, Pizzey JA, Elsom VE, Love D, Davies KE, Walsh FS. Distinct dystrophin mRNA species are expressed in embryonic and adult mouse skeletal muscle. Febs Letters. 242: 47-52. PMID 3060377 DOI: 10.1016/0014-5793(88)80982-7  0.01
1988 Love DR, Fisher R, Bergquist PL. Sequence structure and expression of a cloned β-glucosidase gene from an extreme thermophile Mgg Molecular &Amp; General Genetics. 213: 84-92. PMID 2851713 DOI: 10.1007/BF00333402  0.01
1987 Croft JE, Love DR, Bergquist PL. Expression of leucine genes from an extremely thermophilic bacterium in Escherichia coli Mgg Molecular &Amp; General Genetics. 210: 490-497. PMID 3323845 DOI: 10.1007/BF00327202  0.01
1987 Bergquist PL, Love DR, Croft JE, Streiff MB, Daniel RM, Morgan WH. Genetics and potential biotechnological applications of thermophilic and extremely thermophilic microorganisms Biotechnology and Genetic Engineering Reviews. 5: 199-244. PMID 3314899 DOI: 10.1080/02648725.1987.10647838  0.01
1987 Love DR, Streiff MB. Molecular cloning of a β-glucosidase gene from an extremely thermophilic anaerobe in E couand B. Subtilis Bio/Technology. 5: 384-387. DOI: 10.1038/nbt0487-384  0.01
1984 Lyon A, Love DR. Terminal care: the role of the general practitioner hospital Journal of the Royal College of General Practitioners. 34: 331-333. PMID 6747936  0.01
1972 Brown JJ, Lever AF, Morton JJ, Fraser R, Love DR, Robertson JIS. RAISED PLASMA ANGIOTENSIN II AND ALDOSTERONE DURING DIETARY SODIUM RESTRICTION IN MAN The Lancet. 300: 1106-1107. PMID 4117201 DOI: 10.1016/S0140-6736(72)92714-6  0.01
1972 Brown JJ, Fraser R, Love DR, Ferriss JB, Lever AF, Robertson JIS, Wilson A. APPARENTLY ISOLATED EXCESS DEOXYCORTICOSTERONE IN HYPERTENSION. A Variant of the Mineralocorticoid-excess Syndrome The Lancet. 300: 243-247. PMID 4114505 DOI: 10.1016/S0140-6736(72)91685-6  0.01
1971 Love DR, Brown JJ, Fraser R, Lever AF, Robertson JI, Timbury GC, Thomson S, Tree M. An unusual case of self-induced electrolyte depletion Gut. 12: 284-290. PMID 5574799  0.01
1971 Johnson RH, McLellan DL, Love DR. Orthostatic hypotension and the Holmes-Adie syndrome. A study of two patients with afferent baroreceptor block Journal of Neurology Neurosurgery and Psychiatry. 34: 562-570. PMID 5122384  0.01
1971 Love DR, Brown JJ, Chinn RH, Johnson RH, Lever AF, Park DM, Robertson JI. Plasma renin in idiopathic orthostatic hypotension: differential response in subjects with probable afferent and efferent autonomic failure Clinical Science. 41: 289-299. PMID 4328988  0.01
1968 Love DR. The chicken or the egg New Mexico Dental Journal. 18: 27-31. PMID 5241094  0.01
1961 Phillips RW, Love DR. The Effect of Certain Additive Agents on the Physical Properties of Zinc Oxide-Eugenol Mixtures Journal of Dental Research. 40: 294-303. DOI: 10.1177/00220345610400021201  0.01
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