| Year |
Citation |
Score |
| 2016 |
Alles SR, Bandet MV, Eppler K, Noh MC, Winship IR, Baker G, Ballanyi K, Smith PA. Acute anti-allodynic action of gabapentin in dorsal horn and primary somatosensory cortex: Correlation of behavioural and physiological data. Neuropharmacology. PMID 27856391 DOI: 10.1016/J.Neuropharm.2016.11.011 |
0.663 |
|
| 2006 |
Winship IR, Pakan JM, Todd KG, Wong-Wylie DR. A comparison of ventral tegmental neurons projecting to optic flow regions of the inferior olive vs. the hippocampal formation. Neuroscience. 141: 463-73. PMID 16698184 DOI: 10.1016/j.neuroscience.2006.03.057 |
0.742 |
|
| 2006 |
Winship IR, Wylie DR. Receptive-field structure of optic flow responsive Purkinje cells in the vestibulocerebellum of pigeons. Visual Neuroscience. 23: 115-26. PMID 16597355 DOI: 10.1017/S0952523806231109 |
0.614 |
|
| 2006 |
Winship IR, Crowder NA, Wylie DR. Quantitative reassessment of speed tuning in the accessory optic system and pretectum of pigeons. Journal of Neurophysiology. 95: 546-51. PMID 16192326 DOI: 10.1152/jn.00921.2005 |
0.695 |
|
| 2005 |
Wylie DR, Ogilvie CJ, Crowder NA, Barkley RR, Winship IR. Telencephalic projections to the nucleus of the basal optic root and pretectal nucleus lentiformis mesencephali in pigeons. Visual Neuroscience. 22: 237-47. PMID 15935115 DOI: 10.1017/S0952523805221090 |
0.748 |
|
| 2005 |
Pakan JM, Todd KG, Nguyen AP, Winship IR, Hurd PL, Jantzie LL, Wylie DR. Inferior olivary neurons innervate multiple zones of the flocculus in pigeons (Columba livia). The Journal of Comparative Neurology. 486: 159-68. PMID 15844212 DOI: 10.1002/Cne.20523 |
0.755 |
|
| 2005 |
Winship IR, Hurd PL, Wylie DR. Spatiotemporal tuning of optic flow inputs to the vestibulocerebellum in pigeons: differences between mossy and climbing fiber pathways. Journal of Neurophysiology. 93: 1266-77. PMID 15483061 DOI: 10.1152/Jn.00815.2004 |
0.593 |
|
| 2004 |
Nguyen AP, Spetch ML, Crowder NA, Winship IR, Hurd PL, Wylie DR. A dissociation of motion and spatial-pattern vision in the avian telencephalon: implications for the evolution of "visual streams". The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 24: 4962-70. PMID 15163688 DOI: 10.1523/Jneurosci.0146-04.2004 |
0.679 |
|
| 2003 |
Wylie DR, Brown MR, Winship IR, Crowder NA, Todd KG. Zonal organization of the vestibulocerebellum in pigeons (Columba livia): III. Projections of the translation zones of the ventral uvula and nodulus. The Journal of Comparative Neurology. 465: 179-94. PMID 12949780 DOI: 10.1002/cne.10857 |
0.733 |
|
| 2003 |
Wylie DR, Brown MR, Barkley RR, Winship IR, Crowder NA, Todd KG. Zonal organization of the vestibulocerebellum in pigeons (Columba livia): II. Projections of the rotation zones of the flocculus. The Journal of Comparative Neurology. 456: 140-53. PMID 12509871 DOI: 10.1002/cne.10508 |
0.75 |
|
| 2003 |
Winship IR, Wylie DR. Zonal organization of the vestibulocerebellum in pigeons (Columba livia): I. Climbing fiber input to the flocculus. The Journal of Comparative Neurology. 456: 127-39. PMID 12509870 DOI: 10.1002/cne.10507 |
0.66 |
|
| 2001 |
Winship IR, Wylie DR. Responses of neurons in the medial column of the inferior olive in pigeons to translational and rotational optic flowfields. Experimental Brain Research. 141: 63-78. PMID 11685411 DOI: 10.1007/s002210100845 |
0.639 |
|
| 2000 |
Crowder NA, Winship IR, Wylie DR. Topographic organization of inferior olive cells projecting to translational zones in the vestibulocerebellum of pigeons. The Journal of Comparative Neurology. 419: 87-95. PMID 10717641 DOI: 10.1002/(SICI)1096-9861(20000327)419:1<87::AID-CNE5>3.0.CO;2-W |
0.723 |
|
| 1999 |
Wylie DR, Winship IR, Glover RG. Projections from the medial column of the inferior olive to different classes of rotation-sensitive Purkinje cells in the flocculus of pigeons. Neuroscience Letters. 268: 97-100. PMID 10400087 DOI: 10.1016/S0304-3940(99)00390-0 |
0.638 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2019 |
Catuneanu A, Paylor JW, Winship I, Colbourne F, Kerr BJ. Sex differences in central nervous system plasticity and pain in experimental autoimmune encephalomyelitis. Pain. PMID 30649100 DOI: 10.1097/j.pain.0000000000001483 |
0.236 |
|
| 2016 |
Potter LE, Paylor JW, Suh JS, Tenorio G, Caliaperumal J, Colbourne F, Baker G, Winship I, Kerr BJ. Altered excitatory-inhibitory balance within somatosensory cortex is associated with enhanced plasticity and pain sensitivity in a mouse model of multiple sclerosis. Journal of Neuroinflammation. 13: 142. PMID 27282914 DOI: 10.1186/S12974-016-0609-4 |
0.234 |
|
| 2015 |
Benson C, Paylor JW, Tenorio G, Winship I, Baker G, Kerr BJ. Voluntary wheel running delays disease onset and reduces pain hypersensitivity in early experimental autoimmune encephalomyelitis (EAE). Experimental Neurology. 271: 279-290. PMID 26033473 DOI: 10.1016/J.Expneurol.2015.05.017 |
0.233 |
|
| 2008 |
Winship IR, Murphy TH. In vivo calcium imaging reveals functional rewiring of single somatosensory neurons after stroke. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 28: 6592-606. PMID 18579732 DOI: 10.1523/Jneurosci.0622-08.2008 |
0.226 |
|
| 2021 |
Bandet MV, Dong B, Winship IR. Distinct patterns of activity in individual cortical neurons and local networks in primary somatosensory cortex of mice evoked by square-wave mechanical limb stimulation. Plos One. 16: e0236684. PMID 33914738 DOI: 10.1371/journal.pone.0236684 |
0.224 |
|
| 2009 |
Winship IR, Murphy TH. Remapping the somatosensory cortex after stroke: insight from imaging the synapse to network. The Neuroscientist : a Review Journal Bringing Neurobiology, Neurology and Psychiatry. 15: 507-24. PMID 19622841 DOI: 10.1177/1073858409333076 |
0.224 |
|
| 2015 |
Daude N, Gapeshina H, Dong B, Winship I, Westaway D. Neuroprotective properties of the PrP-like Shadoo glycoprotein assessed in the middle cerebral artery occlusion model of ischemia. Prion. 0. PMID 26516793 DOI: 10.1080/19336896.2015.1105432 |
0.219 |
|
| 2007 |
Winship IR, Plaa N, Murphy TH. Rapid astrocyte calcium signals correlate with neuronal activity and onset of the hemodynamic response in vivo. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 27: 6268-72. PMID 17554000 DOI: 10.1523/Jneurosci.4801-06.2007 |
0.205 |
|
| 2018 |
Wiersma AM, Winship IR. Use of Dextran-based Anterograde Cortical Tracers to Assess the Integrity of the Cortical Spinal Tract. Bio-Protocol. 8: e2862. PMID 34285978 DOI: 10.21769/BioProtoc.2862 |
0.193 |
|
| 2023 |
Gupta SJ, Churchward MA, Todd KG, Winship IR. Pleiotrophin Signals Through ALK Receptor to Enhance the Growth of Neurons in the Presence of Inhibitory Chondroitin Sulfate Proteoglycans. Neuroscience Insights. 18: 26331055231186993. PMID 37465214 DOI: 10.1177/26331055231186993 |
0.188 |
|
| 2020 |
Anderson MD, Paylor JW, Scott GA, Greba Q, Winship IR, Howland JG. ChABC infusions into medial prefrontal cortex, but not posterior parietal cortex, improve the performance of rats tested on a novel, challenging delay in the touchscreen TUNL task. Learning & Memory (Cold Spring Harbor, N.Y.). 27: 222-235. PMID 32414940 DOI: 10.1101/Lm.050245.119 |
0.187 |
|
| 2018 |
Paylor JW, Wendlandt E, Freeman TS, Greba Q, Marks WN, Howland JG, Winship IR. Impaired Cognitive Function after Perineuronal Net Degradation in the Medial Prefrontal Cortex. Eneuro. 5. PMID 30627657 DOI: 10.1523/ENEURO.0253-18.2018 |
0.186 |
|
| 2017 |
Li Y, Lucas-Osma AM, Black S, Bandet MV, Stephens MJ, Vavrek R, Sanelli L, Fenrich KK, Di Narzo AF, Dracheva S, Winship IR, Fouad K, Bennett DJ. Pericytes impair capillary blood flow and motor function after chronic spinal cord injury. Nature Medicine. PMID 28459438 DOI: 10.1038/Nm.4331 |
0.161 |
|
| 1986 |
Hare CE, Winship IR. Using standard software for small-scale library projects: Experience at Newcastle upon Tyne Polytechnic with WordStar and dBase II Program. 20: 62-70. DOI: 10.1108/eb046926 |
0.15 |
|
| 2010 |
Kohonen-Corish MR, Al-Aama JY, Auerbach AD, Axton M, Barash CI, Bernstein I, Béroud C, Burn J, Cunningham F, Cutting GR, den Dunnen JT, Greenblatt MS, Kaput J, Katz M, Lindblom A, ... ... Winship I, et al. How to catch all those mutations--the report of the third Human Variome Project Meeting, UNESCO Paris, May 2010. Human Mutation. 31: 1374-81. PMID 20960468 DOI: 10.1002/Humu.21379 |
0.137 |
|
| 2009 |
Brown CE, Aminoltejari K, Erb H, Winship IR, Murphy TH. In vivo voltage-sensitive dye imaging in adult mice reveals that somatosensory maps lost to stroke are replaced over weeks by new structural and functional circuits with prolonged modes of activation within both the peri-infarct zone and distant sites. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 1719-34. PMID 19211879 DOI: 10.1523/Jneurosci.4249-08.2009 |
0.137 |
|
| 1984 |
Winship I, Gericke G, Beighton P. X-linked inheritance of ocular albinism with late-onset sensorineural deafness. American Journal of Medical Genetics. 19: 797-803. PMID 6542750 DOI: 10.1002/ajmg.1320190421 |
0.134 |
|
| 2024 |
Bandet MV, Winship IR. Aberrant cortical activity, functional connectivity, and neural assembly architecture after photothrombotic stroke in mice. Elife. 12. PMID 38687189 DOI: 10.7554/eLife.90080 |
0.12 |
|
| 1993 |
Winship IM, Babaya M, Ramesar RS. X-linked ocular albinism and sensorineural deafness: linkage to Xp22.3. Genomics. 18: 444-5. PMID 8288253 DOI: 10.1006/geno.1993.1495 |
0.111 |
|
| 2014 |
Li Y, Li L, Stephens MJ, Zenner D, Murray KC, Winship IR, Vavrek R, Baker GB, Fouad K, Bennett DJ. Synthesis, transport, and metabolism of serotonin formed from exogenously applied 5-HTP after spinal cord injury in rats. Journal of Neurophysiology. 111: 145-63. PMID 24068759 DOI: 10.1152/Jn.00508.2013 |
0.108 |
|
| 2016 |
Weilinger NL, Lohman AW, Rakai BD, Ma EM, Bialecki J, Maslieieva V, Rilea T, Bandet MV, Ikuta NT, Scott L, Colicos MA, Teskey GC, Winship IR, Thompson RJ. Metabotropic NMDA receptor signaling couples Src family kinases to pannexin-1 during excitotoxicity. Nature Neuroscience. PMID 26854804 DOI: 10.1038/Nn.4236 |
0.104 |
|
| 2018 |
Wiersma A, Winship I. In vivo Use of Dextran-based Anterograde Cortical Tracers to Assess the Integrity of the Cortical Spinal Tract Bio-Protocol. 8. DOI: 10.21769/bioprotoc.2862 |
0.098 |
|
| 2018 |
Wiersma A, Winship I. In vivo Use of Dextran-based Anterograde Cortical Tracers to Assess the Integrity of the Cortical Spinal Tract Bio-Protocol. 8. DOI: 10.21769/bioprotoc.2463 |
0.098 |
|
| 2013 |
Lai AY, Dibal CD, Armitage GA, Winship IR, Todd KG. Distinct activation profiles in microglia of different ages: a systematic study in isolated embryonic to aged microglial cultures. Neuroscience. 254: 185-95. PMID 24042036 DOI: 10.1016/j.neuroscience.2013.09.010 |
0.096 |
|
| 2015 |
Thorburn KC, Paylor JW, Webber CA, Winship IR, Kerr BJ. Facial hypersensitivity and trigeminal pathology in mice with experimental autoimmune encephalomyelitis (EAE). Pain. PMID 26545087 DOI: 10.1097/j.pain.0000000000000409 |
0.096 |
|
| 2012 |
Ly L, Winship I. X-linked recessive polyfibromatosis manifesting with spontaneous keloid scars and Dupuytren's contracture. The Australasian Journal of Dermatology. 53: 148-50. PMID 22571568 DOI: 10.1111/j.1440-0960.2011.00740.x |
0.091 |
|
| 2014 |
Winship IR. Laser speckle contrast imaging to measure changes in cerebral blood flow. Methods in Molecular Biology (Clifton, N.J.). 1135: 223-35. PMID 24510868 DOI: 10.1007/978-1-4939-0320-7_19 |
0.089 |
|
| 2018 |
MacKay MB, Paylor JW, Wong JTF, Winship IR, Baker GB, Dursun SM. Multidimensional Connectomics and Treatment-Resistant Schizophrenia: Linking Phenotypic Circuits to Targeted Therapeutics. Frontiers in Psychiatry. 9: 537. PMID 30425662 DOI: 10.3389/fpsyt.2018.00537 |
0.088 |
|
| 2015 |
Duong BT, Savarirayan R, Winship I. Incidental diagnosis of HLRCC following investigation for Asperger Syndrome: actionable and actioned. Familial Cancer. PMID 26275867 DOI: 10.1007/s10689-015-9829-5 |
0.084 |
|
| 2016 |
Paylor JW, Lins BR, Greba Q, Moen N, de Moraes RS, Howland JG, Winship IR. Developmental disruption of perineuronal nets in the medial prefrontal cortex after maternal immune activation. Scientific Reports. 6: 37580. PMID 27876866 DOI: 10.1038/srep37580 |
0.083 |
|
| 2021 |
Abbasi-Habashi S, Jickling GC, Winship IR. Immune Modulation as a Key Mechanism for the Protective Effects of Remote Ischemic Conditioning After Stroke. Frontiers in Neurology. 12: 746486. PMID 34956045 DOI: 10.3389/fneur.2021.746486 |
0.083 |
|
| 2003 |
George AM, Oei P, Winship I. False-positive diagnosis of trisomy 21 using fluorescence in situ hybridisation (FISH) on uncultured amniotic fluid cells. Prenatal Diagnosis. 23: 302-5. PMID 12673634 DOI: 10.1002/pd.587 |
0.08 |
|
| 1993 |
Bruce A, Winship I. Radial ray defect and Robin sequence: a new syndrome? Clinical Dysmorphology. 2: 241-4. PMID 8287187 |
0.076 |
|
| 2020 |
Parray A, Ma Y, Alam M, Akhtar N, Salam A, Mir F, Qadri S, Sajitha VP, Priyanka J, Kamran S, Winship IR, Shuaib A. An increase in AMPK/e-NOS signaling and attenuation of MMP-9 may contribute to remote ischemic perconditioning associated neuroprotection in rat model of focal ischemia. Brain Research. 146860. PMID 32353433 DOI: 10.1016/J.Brainres.2020.146860 |
0.074 |
|
| 1999 |
Bassi MT, Ramesar RS, Caciotti B, Winship IM, De Grandi A, Riboni M, Townes PL, Beighton P, Ballabio A, Borsani G. X-linked late-onset sensorineural deafness caused by a deletion involving OA1 and a novel gene containing WD-40 repeats. American Journal of Human Genetics. 64: 1604-16. PMID 10330347 DOI: 10.1086/302408 |
0.074 |
|
| 2020 |
Kalisvaart ACJ, Wilkinson CM, Gu S, Kung TFC, Yager J, Winship IR, van Landeghem FKH, Colbourne F. An update to the Monro-Kellie doctrine to reflect tissue compliance after severe ischemic and hemorrhagic stroke. Scientific Reports. 10: 22013. PMID 33328490 DOI: 10.1038/s41598-020-78880-4 |
0.073 |
|
| 2014 |
Winship IR, Armitage GA, Ramakrishnan G, Dong B, Todd KG, Shuaib A. Augmenting collateral blood flow during ischemic stroke via transient aortic occlusion. Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism. 34: 61-71. PMID 24045399 DOI: 10.1038/jcbfm.2013.162 |
0.072 |
|
| 2014 |
Baskar Jesudasan SJ, Todd KG, Winship IR. Reduced inflammatory phenotype in microglia derived from neonatal rat spinal cord versus brain. Plos One. 9: e99443. PMID 24914808 DOI: 10.1371/journal.pone.0099443 |
0.07 |
|
| 2020 |
Ma J, Ma Y, Shuaib A, Winship IR. Improved collateral flow and reduced damage after remote ischemic perconditioning during distal middle cerebral artery occlusion in aged rats. Scientific Reports. 10: 12392. PMID 32709950 DOI: 10.1038/s41598-020-69122-8 |
0.07 |
|
| 1990 |
Winship IM, Connor JM, Beighton PH. Genetic heterogeneity in tuberous sclerosis: phenotypic correlations. Journal of Medical Genetics. 27: 418-21. PMID 2395158 |
0.07 |
|
| 1985 |
Beighton P, Winship I, Behari D. The ocular form of osteogenesis imperfecta: a new autosomal recessive syndrome. Clinical Genetics. 28: 69-75. PMID 4028503 |
0.067 |
|
| 2024 |
Yu Z, Burback L, Winkler O, Xu L, Dennett L, Vermetten E, Greenshaw A, Li XM, Milne M, Wang F, Cao B, Winship IR, Zhang Y, Chan AW. Alterations in brain network connectivity and subjective experience induced by psychedelics: a scoping review. Frontiers in Psychiatry. 15: 1386321. PMID 38807690 DOI: 10.3389/fpsyt.2024.1386321 |
0.066 |
|
| 1992 |
Farrer LA, Grundfast KM, Amos J, Arnos KS, Asher JH, Beighton P, Diehl SR, Fex J, Foy C, Friedman TB, Greenberg J, Hoth C, Marazita M, Milunsky A, Morell R, ... ... Winship I, et al. Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: First report of the WS consortium American Journal of Human Genetics. 50: 902-913. PMID 1349198 |
0.063 |
|
| 2006 |
Watkins WJ, Harris SE, Craven MJ, Vincent AL, Winship IM, Gersak K, Shelling AN. An investigation into FOXE1 polyalanine tract length in premature ovarian failure. Molecular Human Reproduction. 12: 145-9. PMID 16481406 DOI: 10.1093/molehr/gal017 |
0.063 |
|
| 2010 |
Povey S, Al Aqeel AI, Cambon-Thomsen A, Dalgleish R, den Dunnen JT, Firth HV, Greenblatt MS, Barash CI, Parker M, Patrinos GP, Savige J, Sobrido MJ, Winship I, Cotton RG. Practical guidelines addressing ethical issues pertaining to the curation of human locus-specific variation databases (LSDBs). Human Mutation. 31: 1179-84. PMID 20683926 DOI: 10.1002/humu.21339 |
0.063 |
|
| 2006 |
Longo I, Scala E, Mari F, Caselli R, Pescucci C, Mencarelli MA, Speciale C, Giani M, Bresin E, Caringella DA, Borochowitz ZU, Siriwardena K, Winship I, Renieri A, Meloni I. Autosomal recessive Alport syndrome: an in-depth clinical and molecular analysis of five families. Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association. 21: 665-71. PMID 16338941 DOI: 10.1093/ndt/gfi312 |
0.061 |
|
| 1991 |
Winship IM, Viljoen DL, Leary PM, De Moor MM. Microcephaly-cardiomyopathy: a new autosomal recessive phenotype? Journal of Medical Genetics. 28: 619-21. PMID 1956062 |
0.06 |
|
| 1991 |
Beighton P, Ramesar R, Winship I, Viljoen D, Greenberg J, Young K, Curtis D, Sellars S. Hearing impairment and pigmentary disturbance. Annals of the New York Academy of Sciences. 630: 152-66. PMID 1952586 |
0.06 |
|
| 2015 |
Winship IR. Cerebral collaterals and collateral therapeutics for acute ischemic stroke. Microcirculation (New York, N.Y. : 1994). 22: 228-36. PMID 25351102 DOI: 10.1111/micc.12177 |
0.059 |
|
| 2005 |
Harris SE, Chand AL, Winship IM, Gersak K, Nishi Y, Yanase T, Nawata H, Shelling AN. INHA promoter polymorphisms are associated with premature ovarian failure. Molecular Human Reproduction. 11: 779-84. PMID 16390856 DOI: 10.1093/Molehr/Gah219 |
0.059 |
|
| 2011 |
McKay L, Frydenberg M, Lipton L, Norris F, Winship I. Case report: renal cell carcinoma segregating with a t(2;3)(q37.3;q13.2) chromosomal translocation in an Ashkenazi Jewish family. Familial Cancer. 10: 349-53. PMID 21188539 DOI: 10.1007/s10689-010-9413-y |
0.058 |
|
| 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 |
0.057 |
|
| 2010 |
Dudding TE, Lawrence O, Winship I, Froyen G, Vandewalle J, Scott R, Shelling AN. Array comparative genomic hybridization for the detection of submicroscopic copy number variations of the X chromosome in women with premature ovarian failure. Human Reproduction (Oxford, England). 25: 3159-60; author repl. PMID 20952765 DOI: 10.1093/humrep/deq284 |
0.056 |
|
| 2018 |
Wiersma AM, Winship IR. Induction of Photothrombotic Stroke in the Sensorimotor Cortex of Rats andPreparation of Tissue for Analysis of Stroke Volume andTopographical Cortical Localization of Ischemic Infarct. Bio-Protocol. 8: e2861. PMID 34285977 DOI: 10.21769/BioProtoc.2861 |
0.056 |
|
| 2016 |
Ma J, Ma Y, Dong B, Bandet MV, Shuaib A, Winship IR. Prevention of the collapse of pial collaterals by remote ischemic perconditioning during acute ischemic stroke. Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism. PMID 27909265 DOI: 10.1177/0271678X16680636 |
0.055 |
|
| 2012 |
Salaria M, Burgess T, Setyapranata S, Winship I. Phenotype in novel Xp duplication. American Journal of Medical Genetics. Part A. 158: 2342-6. PMID 22887700 DOI: 10.1002/ajmg.a.35538 |
0.055 |
|
| 2015 |
Ramakrishnan G, Dong B, Todd KG, Shuaib A, Winship IR. Transient Aortic Occlusion Augments Collateral Blood Flow and Reduces Mortality During Severe Ischemia due to Proximal Middle Cerebral Artery Occlusion. Translational Stroke Research. PMID 26706246 DOI: 10.1007/s12975-015-0443-5 |
0.055 |
|
| 2010 |
Armitage GA, Todd KG, Shuaib A, Winship IR. Laser speckle contrast imaging of collateral blood flow during acute ischemic stroke. Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism. 30: 1432-6. PMID 20517321 DOI: 10.1038/jcbfm.2010.73 |
0.055 |
|
| 1990 |
Winship I, Cremin B, Beighton P. Boomerang dysplasia. American Journal of Medical Genetics. 36: 440-3. PMID 2202214 DOI: 10.1002/ajmg.1320360413 |
0.055 |
|
| 2011 |
Gill AJ, Pachter NS, Chou A, Young B, Clarkson A, Tucker KM, Winship IM, Earls P, Benn DE, Robinson BG, Fleming S, Clifton-Bligh RJ. Renal tumors associated with germline SDHB mutation show distinctive morphology. The American Journal of Surgical Pathology. 35: 1578-85. PMID 21934479 DOI: 10.1097/PAS.0b013e318227e7f4 |
0.054 |
|
| 1994 |
Dunnill MG, Richards AJ, Milana G, Mollica F, Atherton D, Winship I, Farrall M, al-Imara L, Eady RA, Pope FM. Genetic linkage to the type VII collagen gene (COL7A1) in 26 families with generalised recessive dystrophic epidermolysis bullosa and anchoring fibril abnormalities. Journal of Medical Genetics. 31: 745-8. PMID 7837248 |
0.053 |
|
| 2015 |
Mann K, Magee J, Guillaud-Bataille M, Blondel C, Bressac-de Paillerets B, Yeatman J, Winship I. Multiple skin hamartomata: a possible novel clinical presentation of SUFU neoplasia syndrome. Familial Cancer. 14: 151-5. PMID 25287320 DOI: 10.1007/s10689-014-9752-1 |
0.053 |
|
| 2014 |
Sist B, Fouad K, Winship IR. Plasticity beyond peri-infarct cortex: spinal up regulation of structural plasticity, neurotrophins, and inflammatory cytokines during recovery from cortical stroke. Experimental Neurology. 252: 47-56. PMID 24291254 DOI: 10.1016/J.Expneurol.2013.11.019 |
0.053 |
|
| 2000 |
Zito I, Morris A, Tyson P, Winship I, Sharp D, Gilbert D, Thiselton DL, Bhattacharya SS, Hardcastle AJ. Sequence variation within the RPGR gene: evidence for a founder complex allele. Human Mutation. 16: 273-4. PMID 10980543 DOI: 10.1002/1098-1004(200009)16:3<273::AID-HUMU19>3.0.CO;2-W |
0.052 |
|
| 1991 |
Winship I, Young K, Martell R, Ramesar R, Curtis D, Beighton P. Piebaldism: an autonomous autosomal dominant entity. Clinical Genetics. 39: 330-7. PMID 1860249 |
0.052 |
|
| 2014 |
Gill AJ, Toon CW, Clarkson A, Sioson L, Chou A, Winship I, Robinson BG, Benn DE, Clifton-Bligh RJ, Dwight T. Succinate dehydrogenase deficiency is rare in pituitary adenomas. The American Journal of Surgical Pathology. 38: 560-6. PMID 24625421 DOI: 10.1097/PAS.0000000000000149 |
0.051 |
|
| 2000 |
Reeve J, Owens RG, Winship IM. Psychological impact of predictive testing for colonic cancer. Journal of Health Psychology. 5: 99-108. PMID 22048828 DOI: 10.1177/135910530000500102 |
0.05 |
|
| 2019 |
Ma J, Ma Y, Shuaib A, Winship IR. Impaired Collateral Flow in Pial Arterioles of Aged Rats During Ischemic Stroke. Translational Stroke Research. PMID 31203565 DOI: 10.1007/s12975-019-00710-1 |
0.049 |
|
| 1986 |
Winship I. Epidermolysis bullosa in South Africa. South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde. 69: 743-6. PMID 3715646 |
0.049 |
|
| 2013 |
Winship IR. Improved cerebral blood flow measurement with multiexposure speckle imaging. Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism. 33: 797. PMID 23571284 DOI: 10.1038/jcbfm.2013.59 |
0.048 |
|
| 2015 |
Huq A, Kentwell M, Tirimacco A, Rossini J, Rawlings L, Winship I. Vestibular schwannoma in a patient with neurofibromatosis type 1: clinical report and literature review. Familial Cancer. 14: 157-60. PMID 25362541 DOI: 10.1007/s10689-014-9763-y |
0.048 |
|
| 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 |
0.048 |
|
| 2014 |
Wain KE, Ellingson MS, McDonald J, Gammon A, Roberts M, Pichurin P, Winship I, Riegert-Johnson DL, Weitzel JN, Lindor NM. Appreciating the broad clinical features of SMAD4 mutation carriers: a multicenter chart review. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 16: 588-93. PMID 24525918 DOI: 10.1038/gim.2014.5 |
0.048 |
|
| 1989 |
Sampson JR, Yates JR, Pirrit LA, Fleury P, Winship I, Beighton P, Connor JM. Evidence for genetic heterogeneity in tuberous sclerosis. Journal of Medical Genetics. 26: 511-6. PMID 2769723 DOI: 10.1136/jmg.26.8.511 |
0.048 |
|
| 2015 |
Smith CM, Jerkovic A, Puy H, Winship I, Deybach JC, Gouya L, van Dooren G, Goodman CD, Sturm A, Manceau H, McFadden GI, David P, Mercereau-Puijalon O, Burgio G, McMorran BJ, et al. Red cells from ferrochelatase-deficient erythropoietic protoporphyria patients are resistant to growth of malarial parasites. Blood. 125: 534-41. PMID 25414439 DOI: 10.1182/Blood-2014-04-567149 |
0.047 |
|
| 2017 |
Wiersma AM, Fouad K, Winship IR. Enhancing spinal plasticity amplifies the benefits of rehabilitative training and improves recovery from stroke. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 29025926 DOI: 10.1523/Jneurosci.0770-17.2017 |
0.047 |
|
| 2021 |
Jesudasan SJB, Gupta SJ, Churchward MA, Todd KG, Winship IR. Inflammatory Cytokine Profile and Plasticity of Brain and Spinal Microglia in Response to ATP and Glutamate. Frontiers in Cellular Neuroscience. 15: 634020. PMID 33889075 DOI: 10.3389/fncel.2021.634020 |
0.046 |
|
| 2013 |
Rudd A, Grant J, Varigos G, Morgan V, Winship I. Co-existence of hereditary coproporphyria and porphyria cutanea tarda: The importance of genetic testing. The Australasian Journal of Dermatology. 54: e50-2. PMID 23582006 DOI: 10.1111/j.1440-0960.2011.00875.x |
0.046 |
|
| 2012 |
Hopper JL, Jenkins MA, Dowty JG, Dite GS, Apicella C, Keogh L, Win AK, Young JP, Buchanan D, Walsh MD, Rosty C, Baglietto L, Severi G, Phillips KA, Wong EM, ... ... Winship I, et al. Using tumour pathology to identify people at high genetic risk of breast and colorectal cancers. Pathology. 44: 89-98. PMID 22198256 DOI: 10.1097/PAT.0b013e32834e8e5b |
0.046 |
|
| 1986 |
Gordon GD, Winship IM, Goldblatt J. Occult life-threatening streptococcal septicaemia in the elderly. A report of 2 cases. South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde. 70: 762-3. PMID 3787407 |
0.046 |
|
| 2006 |
Abbott WG, Winship IM, Gane EJ, Finau SA, Munn SR, Tukuitonga CE. Genetic diversity and linkage disequilibrium in the Polynesian population of Niue Island. Human Biology. 78: 131-45. PMID 17036922 |
0.044 |
|
| 2016 |
Ramakrishnan G, Dong B, Todd KG, Shuaib A, Winship IR. Erratum to: Transient Aortic Occlusion Augments Collateral Blood Flow and Reduces Mortality During Severe Ischemia Due to Proximal Middle Cerebral Artery Occlusion. Translational Stroke Research. PMID 26818735 DOI: 10.1007/s12975-016-0452-z |
0.043 |
|
| 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 |
0.043 |
|
| 2014 |
Sexton A, Rawlings L, Jenkins M, Winship I. Predictive genetic testing of a bone marrow recipient-ethical issues involving unexpected results, gender issues, test accuracy, and implications for the donor. Journal of Genetic Counseling. 23: 33-7. PMID 23990319 DOI: 10.1007/s10897-013-9643-x |
0.043 |
|
| 2013 |
Coory M, White VM, Johnson KS, Hill DJ, Jefford M, Harrison S, Winship I, Millar J, Giles GG. Systematic review of quality improvement interventions directed at cancer specialists. Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. 31: 1583-91. PMID 23530093 DOI: 10.1200/JCO.2012.46.0253 |
0.042 |
|
| 2015 |
Hodgson J, Metcalfe S, Gaff C, Donath S, Delatycki MB, Winship I, Skene L, Aitken M, Halliday J. Outcomes of a randomised controlled trial of a complex genetic counselling intervention to improve family communication. European Journal of Human Genetics : Ejhg. PMID 26130486 DOI: 10.1038/ejhg.2015.122 |
0.042 |
|
| 2013 |
Farrelly A, White V, Meiser B, Jefford M, Young MA, Ieropoli S, Winship I, Duffy J. Unmet support needs and distress among women with a BRCA1/2 mutation. Familial Cancer. 12: 509-18. PMID 23264090 DOI: 10.1007/s10689-012-9596-5 |
0.042 |
|
| 2003 |
Kannu P, Aftimos S, Winship I. Autosomal dominant velopharyngeal insufficiency: father-to-son transmission confirmed. Clinical Genetics. 64: 522-3. PMID 14986834 DOI: 10.1046/j.1399-0004.2003.00171.x |
0.042 |
|
| 2008 |
Winship IM, Dudding TE. Lessons from the skin--cutaneous features of familial cancer. The Lancet. Oncology. 9: 462-72. PMID 18452857 DOI: 10.1016/S1470-2045(08)70126-8 |
0.041 |
|
| 2015 |
Antill YC, Dowty JG, Win AK, Thompson T, Walsh MD, Cummings MC, Gallinger S, Lindor NM, Le Marchand L, Hopper JL, Newcomb PA, Haile RW, Church J, Tucker KM, Buchanan DD, ... ... Winship IM, et al. Lynch syndrome and cervical cancer. International Journal of Cancer. Journal International Du Cancer. PMID 26077226 DOI: 10.1002/Ijc.29641 |
0.04 |
|
| 1985 |
Winship IM. Ehlers-Danlos syndrome in the Western Cape. South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde. 67: 509-11. PMID 3983735 |
0.04 |
|
| 1997 |
Jass JR, Cottier DS, Pokos V, Parry S, Winship IM. Mixed epithelial polyps in association with hereditary non-polyposis colorectal cancer providing an alternative pathway of cancer histogenesis. Pathology. 29: 28-33. PMID 9094174 DOI: 10.1080/00313029700169494 |
0.04 |
|
| 2018 |
Wiersma A, Winship I. Induction of Photothrombotic Stroke in the Sensorimotor Cortex of Rats and Preparation of Tissue for Analysis of Stroke Volume and Topographical Cortical Localization of Ischemic Infarct Bio-Protocol. 8. DOI: 10.21769/BIOPROTOC.2462 |
0.04 |
|
| 2001 |
McGaughran J, Aftimos S, Jefferies C, Winship I. Clinical phenotypes of nine cases of Kabuki syndrome from New Zealand. Clinical Dysmorphology. 10: 257-62. PMID 11665999 |
0.04 |
|
| 2013 |
Kumar S, Peters S, Thompson T, Morgan N, Maccicoca I, Trainer A, Zentner D, Kalman JM, Winship I, Vohra JK. Familial cardiological and targeted genetic evaluation: low yield in sudden unexplained death and high yield in unexplained cardiac arrest syndromes. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 10: 1653-60. PMID 23973953 DOI: 10.1016/j.hrthm.2013.08.022 |
0.039 |
|
| 2012 |
Cicek MS, Cunningham JM, Fridley BL, Serie DJ, Bamlet WR, Diergaarde B, Haile RW, Le Marchand L, Krontiris TG, Younghusband HB, Gallinger S, Newcomb PA, Hopper JL, Jenkins MA, Casey G, ... ... Winship I, et al. Colorectal cancer linkage on chromosomes 4q21, 8q13, 12q24, and 15q22. Plos One. 7: e38175. PMID 22675446 DOI: 10.1371/Journal.Pone.0038175 |
0.039 |
|
| 2009 |
Harris M, Wallace J, Winship I, Hale L, Gardner M. Hereditary renal cell carcinoma: the clue can be in the skin. Internal Medicine Journal. 39: e12-3. PMID 20233231 DOI: 10.1111/j.1445-5994.2009.02098.x |
0.039 |
|
| 2002 |
Harris SE, Chand AL, Winship IM, Gersak K, Aittomäki K, Shelling AN. Identification of novel mutations in FOXL2 associated with premature ovarian failure. Molecular Human Reproduction. 8: 729-33. PMID 12149404 |
0.039 |
|
| 1985 |
Winship IM. Sotos syndrome--autosomal dominant inheritance substantiated. Clinical Genetics. 28: 243-6. PMID 4064361 |
0.038 |
|
| 2007 |
Abbott W, Gane E, Winship I, Munn S, Tukuitonga C. Polymorphism in intron 1 of the interferon-gamma gene influences both serum immunoglobulin E levels and the risk for chronic hepatitis B virus infection in Polynesians. Immunogenetics. 59: 187-95. PMID 17211638 DOI: 10.1007/s00251-006-0184-4 |
0.038 |
|
| 2015 |
Eastaugh AJ, Thompson T, Vohra JK, O'Brien TJ, Winship I. Sudden unexpected death, epilepsy and familial cardiac pathology. Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia. 22: 1594-600. PMID 26195332 DOI: 10.1016/j.jocn.2015.05.002 |
0.037 |
|
| 2014 |
Lolatgis H, Varigos G, Braue A, Scardamaglia L, Boyapati A, Winship I. Halo naevi and café au lait macule regression in a renal transplant patient on immunosuppression. The Australasian Journal of Dermatology. PMID 25178551 DOI: 10.1111/ajd.12188 |
0.037 |
|
| 2002 |
Humar B, Toro T, Graziano F, Müller H, Dobbie Z, Kwang-Yang H, Eng C, Hampel H, Gilbert D, Winship I, Parry S, Ward R, Findlay M, Christian A, Tucker M, et al. Novel germline CDH1 mutations in hereditary diffuse gastric cancer families. Human Mutation. 19: 518-25. PMID 11968084 DOI: 10.1002/Humu.10067 |
0.036 |
|
| 1992 |
Winship I, Beighton P. Phenotypic discriminants in the Waardenburg syndrome. Clinical Genetics. 41: 181-8. PMID 1576755 |
0.036 |
|
| 2014 |
Rosty C, Williamson EJ, Clendenning M, Walters RJ, Win AK, Jenkins MA, Hopper JL, Winship IM, Southey MC, Giles GG, English DR, Buchanan DD. Should the grading of colorectal adenocarcinoma include microsatellite instability status? Human Pathology. 45: 2077-84. PMID 25149551 DOI: 10.1016/j.humpath.2014.06.020 |
0.036 |
|
| 2015 |
Bondavalli D, White SM, Steer A, Pflaumer A, Winship I. Is cardiac rhabdomyoma a feature of Birt Hogg Dubé syndrome? American Journal of Medical Genetics. Part A. 167: 802-4. PMID 25655561 DOI: 10.1002/ajmg.a.36917 |
0.036 |
|
| 2002 |
D'Amato Sizonenko L, Ng D, Oei P, Winship I. Supernumerary marker chromosomes 5: confirmation of a critical region and resultant phenotype. American Journal of Medical Genetics. 111: 19-26. PMID 12124728 DOI: 10.1002/ajmg.10459 |
0.035 |
|
| 2014 |
Hodgson JM, Metcalfe SA, Aitken M, Donath SM, Gaff CL, Winship IM, Delatycki MB, Skene LL, McClaren BJ, Paul JL, Halliday JL. Improving family communication after a new genetic diagnosis: a randomised controlled trial of a genetic counselling intervention. Bmc Medical Genetics. 15: 33. PMID 24628824 DOI: 10.1186/1471-2350-15-33 |
0.035 |
|
| 1991 |
Winship IM, Saxe NP, Hugel H. Primary oxalosis--an unusual cause of livedo reticularis. Clinical and Experimental Dermatology. 16: 367-70. PMID 1794192 |
0.035 |
|
| 2015 |
Farrelly A, White V, Young MA, Jefford M, Ieropoli S, Duffy J, Winship I, Meiser B. Implementing a telephone based peer support intervention for women with a BRCA1/2 mutation. Familial Cancer. PMID 25820212 DOI: 10.1007/s10689-015-9797-9 |
0.035 |
|
| 2013 |
Woad KJ, Prendergast D, Winship IM, Shelling AN. FSH receptor gene variants are rarely associated with premature ovarian failure. Reproductive Biomedicine Online. 26: 396-9. PMID 23419799 DOI: 10.1016/j.rbmo.2013.01.004 |
0.035 |
|
| 2000 |
Iino H, Simms L, Young J, Arnold J, Winship IM, Webb SI, Furlong KL, Leggett B, Jass JR. DNA microsatellite instability and mismatch repair protein loss in adenomas presenting in hereditary non-polyposis colorectal cancer. Gut. 47: 37-42. PMID 10861262 DOI: 10.1136/gut.47.1.37 |
0.034 |
|
| 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 |
0.034 |
|
| 2014 |
Taylor JA, Bondavalli D, Monif M, Yap LM, Winship I. Mal de Meleda in Indonesia: Mutations in the SLURP1 gene appear to be ubiquitous. The Australasian Journal of Dermatology. PMID 25557416 DOI: 10.1111/ajd.12239 |
0.034 |
|
| 2006 |
Blair V, Martin I, Shaw D, Winship I, Kerr D, Arnold J, Harawira P, McLeod M, Parry S, Charlton A, Findlay M, Cox B, Humar B, More H, Guilford P. Hereditary diffuse gastric cancer: diagnosis and management. Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association. 4: 262-75. PMID 16527687 DOI: 10.1016/j.cgh.2005.12.003 |
0.034 |
|
| 2000 |
Lee YC, Wilson CJ, Winship IM, Veale AG. Marfanoid habitus, dysmorphic features, and web neck. Southern Medical Journal. 93: 1197-200. PMID 11142456 |
0.033 |
|
| 2011 |
Win AK, Dowty JG, Antill YC, English DR, Baron JA, Young JP, Giles GG, Southey MC, Winship I, Lipton L, Parry S, Thibodeau SN, Haile RW, Gallinger S, Le Marchand L, et al. Body mass index in early adulthood and endometrial cancer risk for mismatch repair gene mutation carriers. Obstetrics and Gynecology. 117: 899-905. PMID 21422863 DOI: 10.1097/Aog.0B013E3182110Ea3 |
0.033 |
|
| 2014 |
Stupart D, Win AK, Jenkins M, Winship IM, Goldberg P, Ramesar R. Fertility and apparent genetic anticipation in Lynch syndrome. Familial Cancer. 13: 369-74. PMID 24677027 DOI: 10.1007/s10689-014-9714-7 |
0.033 |
|
| 2015 |
Win AK, Reece JC, Buchanan DD, Clendenning M, Young JP, Cleary SP, Kim H, Cotterchio M, Dowty JG, MacInnis RJ, Tucker KM, Winship IM, Macrae FA, Burnett T, Le Marchand L, et al. Risk of colorectal cancer for people with a mutation in both a MUTYH and a DNA mismatch repair gene. Familial Cancer. 14: 575-83. PMID 26202870 DOI: 10.1007/S10689-015-9824-X |
0.033 |
|
| 2011 |
Wright DM, Arnold JL, Parry B, Hulme-Moir M, Winship IM, Parry S. Immunohistochemistry to detect hereditary nonpolyposis colorectal cancer in young patients: the 7-year Auckland experience. Diseases of the Colon and Rectum. 54: 552-8. PMID 21471755 DOI: 10.1007/DCR.0b013e31820e3265 |
0.032 |
|
| 2015 |
Sexton A, Rawlings L, McKavanagh G, Simons K, Winship I. A Novel von Hippel Lindau Gene Intronic Variant and Its Reclassification from VUS to Pathogenic: the Impact on a Large Family. Journal of Genetic Counseling. PMID 26323595 DOI: 10.1007/s10897-015-9875-z |
0.032 |
|
| 2013 |
Win AK, Lindor NM, Winship I, Tucker KM, Buchanan DD, Young JP, Rosty C, Leggett B, Giles GG, Goldblatt J, Macrae FA, Parry S, Kalady MF, Baron JA, Ahnen DJ, et al. Risks of colorectal and other cancers after endometrial cancer for women with Lynch syndrome. Journal of the National Cancer Institute. 105: 274-9. PMID 23385444 DOI: 10.1093/Jnci/Djs525 |
0.031 |
|
| 2011 |
Beitner MM, Winship I, Drummond KJ. Neurosurgical considerations in von Hippel-Lindau disease. Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia. 18: 171-80. PMID 21215639 DOI: 10.1016/j.jocn.2010.04.054 |
0.031 |
|
| 1996 |
Jass JR, Pokos V, Arnold JL, Cottier DS, Jeevaratnam P, Van de Water NS, Browett PJ, Winship IM, Lane MR. Colorectal neoplasms detected colonoscopically in at-risk members of colorectal cancer families stratified by the demonstration of DNA microsatellite instability. Journal of Molecular Medicine (Berlin, Germany). 74: 547-51. PMID 8892060 |
0.031 |
|
| 2011 |
Gill AJ, Pachter NS, Clarkson A, Tucker KM, Winship IM, Benn DE, Robinson BG, Clifton-Bligh RJ. Renal tumors and hereditary pheochromocytoma-paraganglioma syndrome type 4. The New England Journal of Medicine. 364: 885-6. PMID 21366490 DOI: 10.1056/NEJMc1012357 |
0.03 |
|
| 2012 |
Win AK, Lindor NM, Young JP, Macrae FA, Young GP, Williamson E, Parry S, Goldblatt J, Lipton L, Winship I, Leggett B, Tucker KM, Giles GG, Buchanan DD, Clendenning M, et al. Risks of primary extracolonic cancers following colorectal cancer in lynch syndrome. Journal of the National Cancer Institute. 104: 1363-72. PMID 22933731 DOI: 10.1093/Jnci/Djs351 |
0.03 |
|
| 2006 |
James P, Parry S, Arnold J, Winship I. Confirming a diagnosis of hereditary colorectal cancer: the impact of a Familial Bowel Cancer Registry in New Zealand. The New Zealand Medical Journal. 119: U2168. PMID 16998569 |
0.029 |
|
| 2011 |
Win AK, Dowty JG, English DR, Campbell PT, Young JP, Winship I, Macrae FA, Lipton L, Parry S, Young GP, Buchanan DD, MartÃnez ME, Jacobs ET, Ahnen DJ, Haile RW, et al. Body mass index in early adulthood and colorectal cancer risk for carriers and non-carriers of germline mutations in DNA mismatch repair genes. British Journal of Cancer. 105: 162-9. PMID 21559014 DOI: 10.1038/Bjc.2011.172 |
0.028 |
|
| 2022 |
Bui TA, Jickling GC, Winship IR. Neutrophil dynamics and inflammaging in acute ischemic stroke: A transcriptomic review. Frontiers in Aging Neuroscience. 14: 1041333. PMID 36620775 DOI: 10.3389/fnagi.2022.1041333 |
0.028 |
|
| 2015 |
Nguyen-Dumont T, Hammet F, Mahmoodi M, Tsimiklis H, Teo ZL, Li R, Pope BJ, Terry MB, Buys SS, Daly M, Hopper JL, Winship I, Goldgar DE, Park DJ, Southey MC. Mutation screening of PALB2 in clinically ascertained families from the Breast Cancer Family Registry. Breast Cancer Research and Treatment. 149: 547-54. PMID 25575445 DOI: 10.1007/S10549-014-3260-8 |
0.028 |
|
| 2011 |
Dunn R, Varigos G, Winship I. A photographic essay of prolidase deficiency. Clinical Dysmorphology. 20: 194-9. PMID 21760498 DOI: 10.1097/MCD.0b013e3283486cbd |
0.028 |
|
| 2006 |
Chand AL, Ponnampalam AP, Harris SE, Winship IM, Shelling AN. Mutational analysis of BMP15 and GDF9 as candidate genes for premature ovarian failure. Fertility and Sterility. 86: 1009-12. PMID 17027369 DOI: 10.1016/j.fertnstert.2006.02.107 |
0.028 |
|
| 2012 |
Ait Ouakrim D, Boussioutas A, Lockett T, Winship I, Giles GG, Flander LB, Keogh L, Hopper JL, Jenkins MA. Screening practices of unaffected people at familial risk of colorectal cancer. Cancer Prevention Research (Philadelphia, Pa.). 5: 240-7. PMID 22030089 DOI: 10.1158/1940-6207.CAPR-11-0229 |
0.027 |
|
| 2013 |
Southey MC, Teo ZL, Winship I. PALB2 and breast cancer: ready for clinical translation! The Application of Clinical Genetics. 6: 43-52. PMID 23935381 DOI: 10.2147/TACG.S34116 |
0.027 |
|
| 2012 |
Ait Ouakrim D, Lockett T, Boussioutas A, Keogh L, Flander LB, Winship I, Giles GG, Hopper JL, Jenkins MA. Screening practices of Australian men and women categorized as "at or slightly above average risk" of colorectal cancer. Cancer Causes & Control : Ccc. 23: 1853-64. PMID 23011536 DOI: 10.1007/s10552-012-0067-y |
0.027 |
|
| 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 |
0.027 |
|
| 2011 |
Parry S, Win AK, Parry B, Macrae FA, Gurrin LC, Church JM, Baron JA, Giles GG, Leggett BA, Winship I, Lipton L, Young GP, Young JP, Lodge CJ, Southey MC, et al. Metachronous colorectal cancer risk for mismatch repair gene mutation carriers: the advantage of more extensive colon surgery. Gut. 60: 950-7. PMID 21193451 DOI: 10.1136/Gut.2010.228056 |
0.027 |
|
| 2013 |
Dwight T, Mann K, Benn DE, Robinson BG, McKelvie P, Gill AJ, Winship I, Clifton-Bligh RJ. Familial SDHA mutation associated with pituitary adenoma and pheochromocytoma/paraganglioma. The Journal of Clinical Endocrinology and Metabolism. 98: E1103-8. PMID 23633203 DOI: 10.1210/jc.2013-1400 |
0.027 |
|
| 2015 |
Stupart D, Win AK, Jenkins M, Winship IM. Fertility after young onset colorectal cancer: a study of subjects with Lynch syndrome. Colorectal Disease : the Official Journal of the Association of Coloproctology of Great Britain and Ireland. PMID 25754680 DOI: 10.1111/codi.12940 |
0.027 |
|
| 2016 |
Duong BT, Winship I. The role of STK 11 gene testing in individuals with oral pigmentation Australasian Journal of Dermatology. DOI: 10.1111/ajd.12443 |
0.027 |
|
| 2005 |
Harris M, Winship I, Spriggs M. Controversies and ethical issues in cancer-genetics clinics. The Lancet. Oncology. 6: 301-10. PMID 15863378 DOI: 10.1016/S1470-2045(05)70166-2 |
0.026 |
|
| 2006 |
Chow E, Lipton L, Lynch E, D'Souza R, Aragona C, Hodgkin L, Brown G, Winship I, Barker M, Buchanan D, Cowie S, Nasioulas S, du Sart D, Young J, Leggett B, et al. Hyperplastic polyposis syndrome: phenotypic presentations and the role of MBD4 and MYH. Gastroenterology. 131: 30-9. PMID 16831587 DOI: 10.1053/j.gastro.2006.03.046 |
0.026 |
|
| 2021 |
Nomani AZ, Tatuene JK, Rempel JL, Jeerakathil T, Winship I, Khan KA, Buck BH, Shuaib A, Jickling GC. Association of CT-Based Hypoperfusion Index With Ischemic Core Enlargement in Patients With Medium and Large Vessel Stroke. Neurology. PMID 34607925 DOI: 10.1212/WNL.0000000000012855 |
0.026 |
|
| 2014 |
Rosty C, Walsh MD, Lindor NM, Thibodeau SN, Mundt E, Gallinger S, Aronson M, Pollett A, Baron JA, Pearson S, Clendenning M, Walters RJ, Nagler BN, Crawford WJ, Young JP, ... Winship I, et al. High prevalence of mismatch repair deficiency in prostate cancers diagnosed in mismatch repair gene mutation carriers from the colon cancer family registry. Familial Cancer. 13: 573-82. PMID 25117503 DOI: 10.1007/S10689-014-9744-1 |
0.026 |
|
| 2014 |
Win AK, Dowty JG, Cleary SP, Kim H, Buchanan DD, Young JP, Clendenning M, Rosty C, MacInnis RJ, Giles GG, Boussioutas A, Macrae FA, Parry S, Goldblatt J, Baron JA, ... ... Winship IM, et al. Risk of colorectal cancer for carriers of mutations in MUTYH, with and without a family history of cancer. Gastroenterology. 146: 1208-11.e1-5. PMID 24444654 DOI: 10.1053/J.Gastro.2014.01.022 |
0.026 |
|
| 2012 |
Win AK, Young JP, Lindor NM, Tucker KM, Ahnen DJ, Young GP, Buchanan DD, Clendenning M, Giles GG, Winship I, Macrae FA, Goldblatt J, Southey MC, Arnold J, Thibodeau SN, et al. Colorectal and other cancer risks for carriers and noncarriers from families with a DNA mismatch repair gene mutation: a prospective cohort study. Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. 30: 958-64. PMID 22331944 DOI: 10.1200/Jco.2011.39.5590 |
0.026 |
|
| 2014 |
White VM, Young MA, Farrelly A, Meiser B, Jefford M, Williamson E, Ieropoli S, Duffy J, Winship I. Randomized controlled trial of a telephone-based peer-support program for women carrying a BRCA1 or BRCA2 mutation: impact on psychological distress. Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. 32: 4073-80. PMID 25403211 DOI: 10.1200/JCO.2013.54.1607 |
0.025 |
|
| 2013 |
Buchanan DD, Win AK, Walsh MD, Walters RJ, Clendenning M, Nagler B, Pearson SA, Macrae FA, Parry S, Arnold J, Winship I, Giles GG, Lindor NM, Potter JD, Hopper JL, et al. Family history of colorectal cancer in BRAF p.V600E-mutated colorectal cancer cases. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 22: 917-26. PMID 23462926 DOI: 10.1158/1055-9965.Epi-12-1211 |
0.025 |
|
| 2015 |
Dashti SG, Chau R, Ouakrim DA, Buchanan DD, Clendenning M, Young JP, Winship IM, Arnold J, Ahnen DJ, Haile RW, Casey G, Gallinger S, Thibodeau SN, Lindor NM, Le Marchand L, et al. Female Hormonal Factors and the Risk of Endometrial Cancer in Lynch Syndrome. Jama. 314: 61-71. PMID 26151267 DOI: 10.1001/Jama.2015.6789 |
0.025 |
|
| 2015 |
Ait Ouakrim D, Dashti SG, Chau R, Buchanan DD, Clendenning M, Rosty C, Winship IM, Young JP, Giles GG, Leggett B, Macrae FA, Ahnen DJ, Casey G, Gallinger S, Haile RW, et al. Aspirin, Ibuprofen, and the Risk of Colorectal Cancer in Lynch Syndrome. Journal of the National Cancer Institute. 107. PMID 26109217 DOI: 10.1093/Jnci/Djv170 |
0.024 |
|
| 2017 |
Radziwon-Balicka A, Lesyk G, Back V, Fong T, Loredo-Calderon EL, Dong B, El-Sikhry H, El-Sherbani AA, El-Kadi A, Ogg S, Siraki A, Seubert JM, Jose Santos-Martinez M, Radomski MW, Velazquez-Martinez CA, ... Winship IR, et al. Differential Enos-Signalling by Platelet Subpopulations Regulates Adhesion and Aggregation. Cardiovascular Research. PMID 29016749 DOI: 10.1093/Cvr/Cvx179 |
0.024 |
|
| 2005 |
Winship I, Aftimos S. Blepharocheilodontic syndrome or lagophthalmos: a child with overlapping features. Clinical Dysmorphology. 14: 151-3. PMID 15930907 DOI: 10.1097/00019605-200507000-00010 |
0.024 |
|
| 2000 |
Ruttenberg D, Best S, Winship I. Implications for employment in a patient with ocular albinism Journal of Occupational Health and Safety - Australia and New Zealand. 16: 127-129. |
0.024 |
|
| 1988 |
Winship IM, Winship WS. Epidermolysis bullosa misdiagnosed as child abuse. A report of 3 cases. South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde. 73: 369-70. PMID 3353812 |
0.024 |
|
| 2008 |
Smith M, Fawcett S, Sigalas E, Bell R, Devery S, Andrieska N, Winship I. Familial breast cancer: double heterozygosity for BRCA1 and BRCA2 mutations with differing phenotypes. Familial Cancer. 7: 119-24. PMID 17636421 DOI: 10.1007/s10689-007-9154-8 |
0.024 |
|
| 2014 |
Winship I, Braue A. Dermatitis artefacta presenting as a recurrent skin eruption in a patient with 1p36 deletion syndrome. The Australasian Journal of Dermatology. 55: 90. PMID 24433376 DOI: 10.1111/ajd.12131 |
0.023 |
|
| 2013 |
Ingles J, Sarina T, Yeates L, Hunt L, Macciocca I, McCormack L, Winship I, McGaughran J, Atherton J, Semsarian C. Clinical predictors of genetic testing outcomes in hypertrophic cardiomyopathy. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 15: 972-7. PMID 23598715 DOI: 10.1038/gim.2013.44 |
0.023 |
|
| 2013 |
Winship IM, McNeil J, Simes RJ. A funding model for public-good clinical trials. The Medical Journal of Australia. 199: 90-1. PMID 23879491 DOI: 10.5694/mja13.10381 |
0.023 |
|
| 2013 |
Win AK, Parry S, Parry B, Kalady MF, Macrae FA, Ahnen DJ, Young GP, Lipton L, Winship I, Boussioutas A, Young JP, Buchanan DD, Arnold J, Le Marchand L, Newcomb PA, et al. Risk of metachronous colon cancer following surgery for rectal cancer in mismatch repair gene mutation carriers. Annals of Surgical Oncology. 20: 1829-36. PMID 23358792 DOI: 10.1245/S10434-012-2858-5 |
0.023 |
|
| 2008 |
Senter L, Clendenning M, Sotamaa K, Hampel H, Green J, Potter JD, Lindblom A, Lagerstedt K, Thibodeau SN, Lindor NM, Young J, Winship I, Dowty JG, White DM, Hopper JL, et al. The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations. Gastroenterology. 135: 419-28. PMID 18602922 DOI: 10.1053/J.Gastro.2008.04.026 |
0.023 |
|
| 2008 |
Port RV, Arnold J, Kerr D, Glavish N, Gravish N, Winship I. Cultural enhancement of a clinical service to meet the needs of indigenous people; genetic service development in response to issues for New Zealand Maori. Clinical Genetics. 73: 132-8. PMID 18177468 DOI: 10.1111/j.1399-0004.2007.00943.x |
0.023 |
|
| 2014 |
Salaria M, Taylor J, Bogwitz M, Winship I. Hereditary haemorrhagic telangiectasia, an Australian cohort: clinical and investigative features. Internal Medicine Journal. 44: 639-44. PMID 24750312 DOI: 10.1111/imj.12457 |
0.022 |
|
| 2013 |
Teo ZL, Provenzano E, Dite GS, Park DJ, Apicella C, Sawyer SD, James PA, Mitchell G, Trainer AH, Lindeman GJ, Shackleton K, Cicciarelli L, Buys SS, Andrulis IL, ... ... Winship I, et al. Tumour morphology predicts PALB2 germline mutation status. British Journal of Cancer. 109: 154-63. PMID 23787919 DOI: 10.1038/Bjc.2013.295 |
0.022 |
|
| 2010 |
Southey MC, Teo ZL, Dowty JG, Odefrey FA, Park DJ, Tischkowitz M, Sabbaghian N, Apicella C, Byrnes GB, Winship I, Baglietto L, Giles GG, Goldgar DE, Foulkes WD, Hopper JL, et al. A PALB2 mutation associated with high risk of breast cancer. Breast Cancer Research : Bcr. 12: R109. PMID 21182766 DOI: 10.1186/bcr2796 |
0.022 |
|
| 2014 |
Rosty C, Williamson EJ, Clendenning M, Walters RJ, Walsh MD, Win AK, Jenkins MA, Hopper JL, Winship I, Southey MC, Giles GG, English DR, Buchanan DD. Re: Microsatellite instability and BRAF mutation testing in colorectal cancer prognostication. Journal of the National Cancer Institute. 106. PMID 25114271 DOI: 10.1093/jnci/dju180 |
0.022 |
|
| 1999 |
Aftimos S, Winship I. A patient with VACTERL association, amelia and hemifacial microsomia. Clinical Dysmorphology. 8: 135-7. PMID 10319203 |
0.022 |
|
| 1984 |
Winship IR. The gas engine in British agriculture c1870-1925 History of Technology. 9th Annual Volume, 1984. 181-204. |
0.021 |
|
| 2010 |
Baglietto L, Lindor NM, Dowty JG, White DM, Wagner A, Gomez Garcia EB, Vriends AH, Cartwright NR, Barnetson RA, Farrington SM, Tenesa A, Hampel H, Buchanan D, Arnold S, ... ... Winship IM, et al. Risks of Lynch syndrome cancers for MSH6 mutation carriers. Journal of the National Cancer Institute. 102: 193-201. PMID 20028993 DOI: 10.1093/Jnci/Djp473 |
0.021 |
|
| 2008 |
Hopper JL, Dowty JG, Apicella C, Southey MC, Giles GG, Winship I. Towards more effective and equitable genetic testing for BRCA1 and BRCA2 mutation carriers. Journal of Medical Genetics. 45: 409-10. PMID 18456714 DOI: 10.1136/jmg.2008.058057 |
0.021 |
|
| 2018 |
Winship IR, Dursun SM, Baker GB, Balista PA, Kandratavicius L, Maia-de-Oliveira JP, Hallak J, Howland JG. An Overview of Animal Models Related to Schizophrenia. Canadian Journal of Psychiatry. Revue Canadienne De Psychiatrie. 706743718773728. PMID 29742910 DOI: 10.1177/0706743718773728 |
0.021 |
|
| 1987 |
Hayden MR, Goldblatt J, Wallis G, Winship IM, Beighton P. Molecular genetics and Huntington's disease. The South African situation. South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde. 71: 683-6. PMID 2954228 |
0.02 |
|
| 2012 |
Winship I, Win AK. The Australasian Colorectal Cancer Family Registry. The Medical Journal of Australia. 197: 480-1. PMID 23121570 DOI: 10.5694/mja12.11395 |
0.02 |
|
| 2011 |
Ly L, Christie M, Swain S, Winship I, Kelly JW. Melanoma(s) arising in large segmental speckled lentiginous nevi: a case series. Journal of the American Academy of Dermatology. 64: 1190-3. PMID 21571187 DOI: 10.1016/j.jaad.2010.12.019 |
0.02 |
|
| 2015 |
Thompson T, Morgan N, Connell V, Zentner D, Davis A, Pflaumer A, Woodford NWF, Winship I. The role of specialist nurses in cardiac genetics-the victorian experience: Supporting partnerships in care Australian Journal of Advanced Nursing. 33: 53-57. |
0.02 |
|
| 2013 |
Slade C, Bosco J, Unglik G, Bleasel K, Nagel M, Winship I. Deficiency in complement factor B. The New England Journal of Medicine. 369: 1667-9. PMID 24152280 DOI: 10.1056/NEJMc1306326 |
0.02 |
|
| 1994 |
Butt J, Greenberg J, Winship I, Sellars S, Beighton P, Ramesar R. A splice junction mutation in PAX3 causes Waardenburg syndrome in a South African family. Human Molecular Genetics. 3: 197-8. PMID 8162027 |
0.02 |
|
| 2013 |
Teo ZL, Park DJ, Provenzano E, Chatfield CA, Odefrey FA, Nguyen-Dumont T, Dowty JG, Hopper JL, Winship I, Goldgar DE, Southey MC. Prevalence of PALB2 mutations in Australasian multiple-case breast cancer families. Breast Cancer Research : Bcr. 15: R17. PMID 23448497 DOI: 10.1186/bcr3392 |
0.02 |
|
| 2013 |
Kirkman M, Stern C, Neil S, Winship I, Mann GB, Shanahan K, Missen D, Shepherd H, Fisher JR. Fertility management after breast cancer diagnosis: a qualitative investigation of women's experiences of and recommendations for professional care. Health Care For Women International. 34: 50-67. PMID 23216096 DOI: 10.1080/07399332.2012.735729 |
0.019 |
|
| 1997 |
Woodfield MJ, Woodfield DG, Winship IM. Clinical and molecular aspects of Gaucher disease in New Zealand. The New Zealand Medical Journal. 110: 316-9. PMID 9315031 |
0.018 |
|
| 2006 |
Watkins WJ, Umbers AJ, Woad KJ, Harris SE, Winship IM, Gersak K, Shelling AN. Mutational screening of FOXO3A and FOXO1A in women with premature ovarian failure. Fertility and Sterility. 86: 1518-21. PMID 16979636 DOI: 10.1016/j.fertnstert.2006.03.054 |
0.017 |
|
| 2013 |
Winship IM, Tucker K. The utility of genetics in inherited cancer. The Medical Journal of Australia. 199: 644. PMID 24237079 DOI: 10.5694/Mja13.10978 |
0.017 |
|
| 2015 |
Zentner D, Thompson TN, James PA, Trainer A, Adès LC, Macciocca I, Taylor JA, Mann K, Bogwitz M, Lewis N, Morgan N, Vohra J, Winship I. The Cardiac Genetics Clinic: a model for multidisciplinary genomic medicine. The Medical Journal of Australia. 203: 261. PMID 26377294 DOI: 10.5694/mja14.01674 |
0.017 |
|
| 2011 |
Southey MC, Ramus SJ, Dowty JG, Smith LD, Tesoriero AA, Wong EE, Dite GS, Jenkins MA, Byrnes GB, Winship I, Phillips KA, Giles GG, Hopper JL. Morphological predictors of BRCA1 germline mutations in young women with breast cancer. British Journal of Cancer. 104: 903-9. PMID 21343941 DOI: 10.1038/bjc.2011.41 |
0.017 |
|
| 2013 |
Win AK, Hopper JL, Buchanan DD, Young JP, Tenesa A, Dowty JG, Giles GG, Goldblatt J, Winship I, Boussioutas A, Young GP, Parry S, Baron JA, Duggan D, Gallinger S, et al. Are the common genetic variants associated with colorectal cancer risk for DNA mismatch repair gene mutation carriers? European Journal of Cancer (Oxford, England : 1990). 49: 1578-87. PMID 23434150 DOI: 10.1016/J.Ejca.2013.01.029 |
0.017 |
|
| 2014 |
Peters SA, Laham SM, Pachter N, Winship IM. The future in clinical genetics: affective forecasting biases in patient and clinician decision making. Clinical Genetics. 85: 312-7. PMID 23952534 DOI: 10.1111/cge.12255 |
0.016 |
|
| 2015 |
Sexton A, Rawlings L, McKavanagh G, Simons K, Winship I. A Novel von Hippel Lindau Gene Intronic Variant and Its Reclassification from VUS to Pathogenic: the Impact on a Large Family Journal of Genetic Counseling. DOI: 10.1007/s10897-015-9875-z |
0.016 |
|
| 2019 |
Howland JG, Greenshaw AJ, Winship IR. Practical Aspects of Animal Models of Psychiatric Disorders. Canadian Journal of Psychiatry. Revue Canadienne De Psychiatrie. 64: 3-4. PMID 30789052 DOI: 10.1177/0706743718771833 |
0.016 |
|
| 1996 |
Jass JR, Arnold JL, Winship IM. Impact of molecular genetics on the management of familial adenomatous polyposis. The New Zealand Medical Journal. 109: 285-6. PMID 8773669 |
0.016 |
|
| 2014 |
Kirkman M, Winship I, Stern C, Neil S, Mann GB, Fisher JR. Women's reflections on fertility and motherhood after breast cancer and its treatment. European Journal of Cancer Care. 23: 502-13. PMID 24417674 DOI: 10.1111/ecc.12163 |
0.016 |
|
| 2015 |
Nguyen-Dumont T, Winship I, Southey MC. Interpretation of genomic variation and disease association: the great missense mutation challenge! Breast Cancer Research and Treatment. 151: 475-6. PMID 25900795 DOI: 10.1007/s10549-015-3394-3 |
0.015 |
|
| 2013 |
Wee R, Henaghan M, Winship I. Dynamic consent in the digital age of biology: online initiatives and regulatory considerations. Journal of Primary Health Care. 5: 341-7. PMID 24294625 |
0.015 |
|
| 2015 |
Winship I. Precision medicine: are we there? The Medical Journal of Australia. 203: 132-3, 133e.1. PMID 26224178 DOI: 10.5694/mja15.00236 |
0.013 |
|
| 2001 |
Trembath RC, Thomson JR, Machado RD, Morgan NV, Atkinson C, Winship I, Simonneau G, Galie N, Loyd JE, Humbert M, Nichols WC, Morrell NW, Berg J, Manes A, McGaughran J, et al. Clinical and molecular genetic features of pulmonary hypertension in patients with hereditary hemorrhagic telangiectasia. The New England Journal of Medicine. 345: 325-34. PMID 11484689 DOI: 10.1056/Nejm200108023450503 |
0.01 |
|
| 1995 |
Winship IR. World-Wide Web searching tools: An evaluation Vine. 25: 49-54. DOI: 10.1108/eb040568 |
0.01 |
|
| 2014 |
Salaria M, Mitchell P, Winship I. Author reply: To PMID 24750312. Internal Medicine Journal. 44: 1048. PMID 25302729 DOI: 10.1111/imj.12555 |
0.01 |
|
| 2012 |
Ly L, Winship I, Kelly JW. Reply Journal of the American Academy of Dermatology. 66: 325-326. DOI: 10.1016/j.jaad.2011.08.029 |
0.01 |
|
| 2011 |
Winship IM. William Sinclair Winship. South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde. 101: 632. PMID 21920171 |
0.01 |
|
| 2009 |
Winship I, Ross G, Nicoll A, Hogan C, Leong Y, Varigos G. Antioxidant effect of warfarin therapy: a possible symptomatic treatment for erythropoietic protoporphyria. Archives of Dermatology. 145: 960-1. PMID 19687444 DOI: 10.1001/archdermatol.2009.165 |
0.01 |
|
| 2005 |
Kannu P, Winship I, Aftimos S. Further case report of a child with a 9q34 deletion and a review of the reported cases. American Journal of Medical Genetics. Part A. 133: 219-21. PMID 15633185 DOI: 10.1002/ajmg.a.30507 |
0.01 |
|
| 2004 |
Abbott WG, Winship IM, Wilsher ML, Nilau M, Tukuitonga CF. Asthma phenotypes in Niue Islanders. Respirology (Carlton, Vic.). 9: 521-7. PMID 15612965 DOI: 10.1111/j.1440-1843.2004.00601.x |
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 |
|
| 2001 |
Winship I, McNab A. The student's guide to the Internet 2000-2001 (3rd ed.) Online Information Review. 25: 69. |
0.01 |
|
| 2001 |
Criddle S, McNab A, Ormes S, Winship I. The public librarian's guide to the Internet Online Information Review. 25: 68. |
0.01 |
|
| 2000 |
Burton KA, Van Ee CC, Purcell K, Winship I, Shelling AN. Autosomal translocation associated with premature ovarian failure. Journal of Medical Genetics. 37: E2. PMID 10807701 |
0.01 |
|
| 2000 |
Winship I. Achieving Cultural Change in Networked Libraries20002Edited by Bruce Reid and William Foster. Achieving Cultural Change in Networked Libraries. Aldershot: Gower Publishing 2000. 304 pp., ISBN: ISBN 0566082004 £55.00 (cloth) Online Information Review. 24: 255-267. DOI: 10.1108/oir.2000.24.3.255.2 |
0.01 |
|
| 1998 |
Winship I, Bradley P, Barker AL, Salter D. REVIEWS Online and Cd-Rom Review. 22: 349-353. DOI: 10.1108/eb024690 |
0.01 |
|
| 1997 |
Lowood H, Cutcliffe SH, Harkanyi K, Harshbarger P, Launius R, Winship I. Current Bibliography in the History of Technology (1995) Technology and Culture. 38: 1. DOI: 10.2307/3106997 |
0.01 |
|
| 1996 |
qass JR, Pokos V, Winship IM. Current issues in the management of hereditary nonpolyposis colorectal cancer. The New Zealand Medical Journal. 109: 197-8. PMID 8668296 |
0.01 |
|
| 1996 |
Lowood H, Cutcliffe SH, Harkanyi K, Launius R, Winship I. Current Bibliography in the History of Technology (1994) Technology and Culture. 37: 1. DOI: 10.2307/3107088 |
0.01 |
|
| 1995 |
Lowood H, Cutcliffe SH, Harkanyi K, Launius R, Winship I. Current Bibliography in the History of Technology (1993) Technology and Culture. 36: 1. DOI: 10.2307/3106697 |
0.01 |
|
| 1995 |
McNab AS, Winship IR. How to find out about new resources on the Internet New Review of Information Networking. 1: 147-153. DOI: 10.1080/13614579509516854 |
0.01 |
|
| 1994 |
Lowood H, Adams JA, Cutcliffe SH, Harkanyi K, Winship I. Current Bibliography in the History of Technology (1992) Technology and Culture. 35: 1. DOI: 10.2307/3106250 |
0.01 |
|
| 1993 |
Lowood H, Adams JA, Cutcliffe SH, Harkanyi K, Winship I. Current Bibliography in the History of Technology (1991) Technology and Culture. 34: 1. DOI: 10.2307/3106496 |
0.01 |
|
| 1992 |
Lowood H, Adams JA, Cutcliffe SH, Morley J, Roysdon CM, Winship I. Current Bibliography in the History of Technology (1990) Technology and Culture. 33: 1. DOI: 10.2307/3105706 |
0.01 |
|
| 1991 |
Beighton P, Viljoen D, Winship I, Beighton G, Sellars S. Profound childhood deafness in southern Africa. Annals of the New York Academy of Sciences. 630: 290-1. PMID 1952609 |
0.01 |
|
| 1991 |
Lowood H, Adams JA, Cutcliffe SH, Morley J, Roysdon CM, Winship I. Current Bibliography in the History of Technology (1989) Technology and Culture. 32: 659. DOI: 10.2307/3106149 |
0.01 |
|
| 1990 |
Lowood H, Adams JA, Cutcliffe SH, Morley J, Roysdon CM, Winship I. Current Bibliography in the History of Technology (1988) Technology and Culture. 31: 561. DOI: 10.2307/3106098 |
0.01 |
|
| 1989 |
WINSHIP I. Hidden increases Nature. 342: 730-730. DOI: 10.1038/342730d0 |
0.01 |
|
| 1989 |
Winship I. Hidden increases [7] Nature. 342: 730. |
0.01 |
|
| 1988 |
Cutcliffe SH, Roysdon CM, Adams JA, Morley J, Rodriquez L, Winship I. Current Bibliography in the History of Technology (1986) Technology and Culture. 29: 338. DOI: 10.2307/3105563 |
0.01 |
|
| 1981 |
Winship IR. Use the library [4] Nature. 291: 186. DOI: 10.1038/291186d0 |
0.01 |
|
| 1976 |
Winship I. Physics students and information sources Physics Education. 11: 362-364. DOI: 10.1088/0031-9120/11/5/010 |
0.01 |
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