Items where Author is "Knight, Jo"
Journal Article
Pouget, Jennie G. and Giratallah, Haidy and Langlois, Alec W. R. and El-Boraie, Ahmed and Lerman, Caryn and Knight, Jo and Cox, Lisa Sanderson and Nollen, Nikki L. and Ahluwalia, Jasjit S. and Benner, Christian and Chenoweth, Meghan J. and Tyndale, Rachel F. (2025) Fine-mapping the CYP2A6 regional association with nicotine metabolism among African American smokers. Molecular Psychiatry, 30 (3). pp. 943-953. ISSN 1359-4184
Preston, Nancy and Cockshott, Zoë and Russell, Siân and Stocker, Rachel and Knight, Jo and Mason, Suzanne and Hanratty, Barbara (2025) Dying in residential care homes during the early COVID-19 pandemic : a qualitative interview study. BMC Geriatrics, 25 (1): 126. ISSN 1471-2318
Mountain, Rachael and Gatheral, Timothy and Haslam, Patrick and Heys, Kelly and Knight, Jo (2025) Measuring Diagnostic Quality : The Capacity of Routinely Collected Data and Applications to Chronic Respiratory Disease. Pragmatic and Observational Research, 16. pp. 1-6. ISSN 1179-7266
Knight, Jo and Chandrabalan, Vishnu Vardhan and Emsley, Hedley CA (2024) Visualising patient pathways and identifying data repositories in a UK neuroscience centre : Exploratory Study. JMIR Medical Informatics, 12: e60017. ISSN 2291-9694
Yuille, Andy and Davies, Jessica and Green, Mark and Hardman, Charlotte and Knight, Jo and Marshall, Rachel and Armitt, Hannah and Bane, Miranda and Bush, Alex and Carr, Victoria and Clark, Rebecca and Cox, Sally and Crotty, Felicity and de Bell, Sian and Edwards, Annabelle and Ferguson, Jody and Fry, Rich and Goddard, Mark and Harrod, Andy and Hoyle, Helen E. and Irvine, Katherine and Lambrick, Danielle and Leonardi, Nicoletta and Lomas, Michael and Lumber, Ryan and MacLean, Laura and Manoli, Gabriele and Mead, Bethan and Neilson, Louise and Nicholls, Beth and O'Brien, Liz and Pateman, Rachel and Pocock, Michael and Scoffham, Hayley and Sims, Jamie and White, Piran (2024) Moving from features to functions : Bridging disciplinary understandings of urban environments to support healthy people and ecosystems. Health and Place, 90: 103368. ISSN 1353-8292
Chenoweth, Meghan J. and Kim, Yong Jae and Nollen, Nikki L. and Hawk, Larry W. and Mahoney, Martin C. and Lerman, Caryn and Knight, Jo and Tyndale, Rachel F. (2024) Genetic Prediction of Smoking Cessation Medication Side Effects : A Genome‐Wide Investigation of Abnormal Dreams on Varenicline. Clinical pharmacology and therapeutics, 115 (6). pp. 1277-1281. ISSN 0009-9236
Garner, Alex and Preston, Nancy and Caiado, Camila C S and Stubington, Emma and Hanratty, Barbara and Limb, James and Mason, Suzanne M and Knight, Jo (2024) Understanding health service utilisation patterns for care home residents during the COVID-19 pandemic using routinely collected healthcare data. BMC Geriatrics, 24 (1): 449. ISSN 1471-2318
Cockshott, Zoë and Russell, Siân and Stocker, Rachel and Knight, Jo and Mason, Suzanne and Hanratty, Barbara and Preston, Nancy (2024) ‘In the shower crying…but we came back in the following day and did it all again’ : Distress and resilience in care home staff during the COVID-19 pandemic– A qualitative interview study. BMC Geriatrics, 24 (1): 286. ISSN 1471-2318
Langlois, Alec W. R. and Pouget, Jennie G. and Knight, Jo and Chenoweth, Meghan J. and Tyndale, Rachel F. (2024) Associating CYP2A6 structural variants with ovarian and lung cancer risk in the UK Biobank : replication and extension. European Journal of Human Genetics, 32 (3). pp. 357-360. ISSN 1018-4813
Garner, Alex and Lewis, Jen and Dixon, Simon and Preston, Nancy and Caiado, Camila C S and Hanratty, Barbara and Jones, Monica and Knight, Jo and Mason, Suzanne M (2024) The impact of digital technology in care homes on unplanned secondary care usage and associated costs. Age and Ageing: afae004. ISSN 0002-0729
Mountain, Rachael and Knight, Jo and Heys, Kelly and Giorgi, Emanuele and Gatheral, Timothy (2024) Spatio-temporal modelling of referrals to outpatient respiratory clinics in the integrated care system of the Morecambe Bay area, England. BMC Health Services Research, 24 (1): 229. ISSN 1472-6963
Giratallah, Haidy and Chenoweth, Meghan J and Pouget, Jennie G and El-Boraie, Ahmed and Alsaafin, Alaa and Lerman, Caryn and Knight, Jo and Tyndale, Rachel F (2024) CYP2A6 associates with respiratory disease risk and younger age of diagnosis : a phenome-wide association Mendelian randomization study. Human Molecular Genetics, 33 (2). pp. 198-210. ISSN 0964-6906
Biggin, Fran and Ashcroft, Quinta and Howcroft, Timothy and Knight, Jo and Emsley, Hedley (2023) Discovering patterns in outpatient neurology appointments using state sequence analysis. BMC Health Services Research, 23 (1): 1208. ISSN 1472-6963
Langlois, Alec W R and El-Boraie, Ahmed and Pouget, Jennie G and Cox, Lisa Sanderson and Ahluwalia, Jasjit S and Fukunaga, Koya and Mushiroda, Taisei and Knight, Jo and Chenoweth, Meghan J and Tyndale, Rachel F (2023) Genotyping, characterization, and imputation of known and novel CYP2A6 structural variants using SNP array data. Journal of Human Genetics, 68. pp. 533-541. ISSN 1434-5161
Biggin, Fran and Knight, Jo and Dayanandan, Rejith and Marson, Anthony and Wilson, Martin and Nitkunan, Arani and Rog, David and Kipps, Christopher and Mummery, Catherine and Williams, Adrian and Emsley, Hedley C A (2023) Outpatient neurology diagnostic coding : a proposed scheme for standardised implementation. Practical Neurology, 23 (4). pp. 317-322. ISSN 1474-7758
Chenoweth, Meghan J and Lerman, Caryn and Knight, Jo and Tyndale, Rachel F (2023) Influence of CYP2A6 genetic variation, nicotine dependence severity, and treatment on smoking cessation success. Nicotine and Tobacco Research, 25 (6). pp. 1207-1211. ISSN 1462-2203
Isba, Rachel and Brennan, Louise and Davies, Nigel and Knight, Jo (2022) Measles, mumps, and rubella vaccination coverage in children younger than 5 years attending a paediatric emergency department in Manchester, UK : a cross-sectional observational study. The Lancet, 400 (Suppl ). S51. ISSN 0140-6736
Garner, Alex and Knight, Jo and Preston, Nancy and Dixon, Simon and Watchorn, Sam and Caiado, Camila and McShane, Catherine and King, Graham and Mason, Suzanne (2022) Impact of digital technology in care homes on Emergency Department attendances. Emergency Medicine Journal, 39 (12): A974. ISSN 1472-0205
Prentice, Sheryl and Rayson, Paul and Knight, Jo and El-Haj, Mahmoud and Elstein, Solly (2022) A Domain Based Approach to Semantic Lexicon Expansion. International Journal of Lexicography, 35 (3). pp. 364-377.
Langlois, Alec W R and El-Boraie, Ahmed and Fukunaga, Koya and Mushiroda, Taisei and Kubo, Michiaki and Lerman, Caryn and Knight, Jo and Scherer, Steven E and Chenoweth, Meghan J and Tyndale, Rachel F (2022) Accuracy and applications of sequencing and genotyping approaches for CYP2A6 and homologous genes. Pharmacogenetics and genomics, 32 (4). pp. 159-172. ISSN 1744-6880
Chenoweth, Meghan J and Peng, Annie R and Zhu, Andy Z X and Cox, Lisa Sanderson and Nollen, Nikki L and Ahluwalia, Jasjit S and Benowitz, Neal L and Knight, Jo and Swardfager, Walter and Tyndale, Rachel F (2022) Does sex alter the relationship between CYP2B6 variation, hydroxybupropion concentration and bupropion-aided smoking cessation in African Americans? : A moderated mediation analysis. Addiction, 117 (6). pp. 1715-1724. ISSN 0965-2140
Isba, Rachel and Davies, Nigel and Knight, Jo (2021) Are child health information services a viable source of accurate vaccination data for clinicians working in paediatric emergency departments in England? BMJ Health Care and Informatics, 28 (1): e100486. ISSN 2632-1009
El-Boraie, Ahmed and Chenoweth, Meghan J and Pouget, Jennie G and Benowitz, Neal L and Fukunaga, Koya and Mushiroda, Taisei and Kubo, Michiaki and Nollen, Nicole L and Cox, Lisa Sanderson and Lerman, Caryn and Knight, Jo and Tyndale, Rachel F (2021) Transferability Of Ancestry-Specific And Cross-Ancestry CYP2A6 Activity Genetic Risk Scores In African And European Populations. Clinical pharmacology and therapeutics, 110 (4). pp. 975-985. ISSN 0009-9236
Chenoweth, Meghan J and Lerman, Caryn and Knight, Jo and Tyndale, Rachel F (2021) A genome-wide association study of nausea incidence in varenicline-treated cigarette smokers. Nicotine and Tobacco Research, 23 (10). pp. 1805-1809. ISSN 1462-2203
Prentice, Sheryl and Knight, Jo and Rayson, Paul and El-Haj, Mahmoud and Rutherford, Nathan (2021) Problematising Characteristicness : A Biomedical Association Case Study. International Journal of Corpus Linguistics, 26 (3). pp. 305-335. ISSN 1384-6655
Biggin, Frances and Howcroft, Timothy and Davies, Quinta and Knight, Jo and Emsley, Hedley (2021) Variation in waiting times by diagnostic category : an observational study of 1,951 referrals to a neurology outpatient clinic. BMJ Neurology Open, 3 (1): 000133. ISSN 2632-6140
Wall, Jasmine and Knight, Jo and Emsley, Hedley C.A. (2021) Late-onset epilepsy predicts stroke : Systematic review and meta-analysis. Epilepsy and Behavior, 115: 107634. ISSN 1525-5050
Johnson, Olatunji and Knight, Jo and Giorgi, Emanuele (2021) A modelling framework for developing early warning systems of COPD emergency admissions. Spatial and Spatio-temporal Epidemiology, 36: 100392. ISSN 1877-5845
Biggin, Frances and Emsley, Hedley and Knight, Jo (2020) Routinely collected patient data in neurology research : a systematic mapping review. BMC Neurology, 20: 431. ISSN 1471-2377
Kemp, Mike and Biggin, Fran and Dayanandan, Rejith and Knight, Jo and Emsley, Hedley C A (2020) COVID-19 exposes the urgent need for coding of outpatient neurology episodes. BMJ Neurology Open, 2 (2): e000080. ISSN 2632-6140
Winterburn, Julie L and Voineskos, Aristotle N and Devenyi, Gabriel A and Plitman, Eric and de la Fuente-Sandoval, Camilo and Bhagwat, Nikhil and Graff-Guerrero, Ariel and Knight, Jo and Chakravarty, M Mallar (2019) Can we accurately classify schizophrenia patients from healthy controls using magnetic resonance imaging and machine learning? : A multi-method and multi-dataset study. Schizophrenia Research, 214. pp. 3-10. ISSN 0920-9964
Saeed Mirza, Saira and Saeed, Usman and Knight, Jo and Ramirez, Joel and Stuss, Donald and Keith, Julia and Nestor, Sean M. and Yu, Di and Swardfager, Walter and Rogaeva, Ekaterina and George-Hyslop, Peter St. and Black, Sandra E. and Masellis, Mario (2019) APOE-ɛ4, white matter hyperintensities, and cognition in Alzheimer and Lewy body dementia. Neurology, 93 (19). e1807-e1819. ISSN 0028-3878
Pouget, Jennie G and Han, Buhm and Wu, Yang and Mignot, Emmanuel and Ollila, Hanna M and Barker, Jonathan and Spain, Sarah and Dand, Nick and Trembath, Richard and Martin, Javier and Mayes, Maureen D and Bossini-Castillo, Lara and López-Isac, Elena and Jin, Ying and Santorico, Stephanie A and Spritz, Richard A and Hakonarson, Hakon and Polychronakos, Constantin and Raychaudhuri, Soumya and Knight, Jo (2019) Cross-disorder analysis of schizophrenia and 19 immune-mediated diseases identifies shared genetic risk. Human Molecular Genetics, 28 (20). pp. 3498-3513. ISSN 0964-6906
Rhodes, Christopher J and Batai, Ken and Bleda, Marta and Haimel, Matthias and Southgate, Laura and Germain, Marine and Pauciulo, Michael W and Hadinnapola, Charaka and Aman, Jurjan and Girerd, Barbara and Arora, Amit and Knight, Jo and Hanscombe, Ken B and Karnes, Jason H and Kaakinen, Marika and Gall, Henning and Ulrich, Anna and Harbaum, Lars and Cebola, Inês and Ferrer, Jorge and Lutz, Katie and Swietlik, Emilia M and Ahmad, Ferhaan and Amouyel, Philippe and Archer, Stephen L and Argula, Rahul and Austin, Eric D and Badesch, David and Bakshi, Sahil and Barnett, Christopher and Benza, Raymond and Bhatt, Nitin and Bogaard, Harm J and Burger, Charles D and Chakinala, Murali and Church, Colin and Coghlan, John G and Condliffe, Robin and Corris, Paul A and Danesino, Cesare and Debette, Stéphanie and Elliott, C Gregory and Elwing, Jean and Eyries, Melanie and Fortin, Terry and Franke, Andre and Frantz, Robert P and Frost, Adaani and Garcia, Joe G N and Ghio, Stefano (2019) Genetic determinants of risk in pulmonary arterial hypertension : international genome-wide association studies and meta-analysis. Lancet Respiratory Medicine, 7 (3). pp. 227-238. ISSN 2213-2600
Saeed, Usman and Mirza, Saira S. and MacIntosh, Bradley J. and Herrmann, Nathan and Keith, Julia and Ramirez, Joel and Nestor, Sean M. and Yu, Qinggang and Knight, Jo and Swardfager, Walter and Potkin, Steven G. and Rogaeva, Ekaterina and George-Hyslop, Peter St. and Black, Sandra E. and Masellis, Mario (2018) APOE-ε4 associates with hippocampal volume, learning, and memory across the spectrum of Alzheimer's disease and dementia with Lewy bodies. Alzheimer's and Dementia, 14 (9). pp. 1137-1147. ISSN 1552-5260
Patel, Sejal and Patel, Raihaan and Park, Min Tae M. and Masellis, Mario and Knight, Jo and Chakravarty, M. Mallar (2018) Heritability estimates of cortical anatomy : The influence and reliability of different estimation strategies. NeuroImage, 178. pp. 78-91. ISSN 1053-8119
Knight, Jo and King, Nicholas Simon (2018) Connected Health Cities – Lancaster – the north west coast and beyond. Morecambe Bay Medical Journal, 7 (12). p. 310. ISSN 1466-707X
Gonçalves, Vanessa F and Giamberardino, Stephanie N and Crowley, James J and Vawter, Marquis P and Saxena, Richa and Bulik, Cynthia M and Yilmaz, Zeynep and Hultman, Christina M and Sklar, Pamela and Kennedy, James L and Sullivan, Patrick F and Knight, Jo (2018) Examining the role of common and rare mitochondrial variants in schizophrenia. PLoS ONE, 13 (1): e0191153. ISSN 1932-6203
Masellis, Mario and Knight, Jo (2018) Unraveling DNA sequence to identify cerebral indicators of dementia risk. Neurology, 90 (3). p. 109. ISSN 0028-3878
Felsky, Daniel and Xu, Jishu and Chibnik, Lori and Schneider, Julie and Knight, Jo and Kennedy, James L. and Bennett, David A. and De Jager, Philip L. and Voineskos, Aristotle N. (2017) Genetic epistasis regulates amyloid deposition in resilient aging. Alzheimer's and Dementia, 13 (10). pp. 1107-1116. ISSN 1552-5260
Patel, Sejal and Park, Min Tae M. and Devenyi, Gabriel A. and Patel, Raihaan and Masellis, Mario and Knight, Jo and Chakravarty, M. Mallar (2017) Heritability of hippocampal subfield volumes using a twin and non-twin siblings design. Human Brain Mapping, 38 (9). pp. 4337-4352. ISSN 1065-9471
Huang, Hailiang and Fang, Ming and Jostins, Luke and Umićević Mirkov, Maša and Boucher, Gabrielle and Anderson, Carl A and Andersen, Vibeke and Cleynen, Isabelle and Cortes, Adrian and Crins, François and D'Amato, Mauro and Deffontaine, Valérie and Dmitrieva, Julia and Docampo, Elisa and Elansary, Mahmoud and Farh, Kyle Kai-How and Franke, Andre and Gori, Ann-Stephan and Goyette, Philippe and Halfvarson, Jonas and Haritunians, Talin and Knight, Jo and Lawrance, Ian C and Lees, Charlie W and Louis, Edouard and Mariman, Rob and Meuwissen, Theo and Mni, Myriam and Momozawa, Yukihide and Parkes, Miles and Spain, Sarah L and Théâtre, Emilie and Trynka, Gosia and Satsangi, Jack and van Sommeren, Suzanne and Vermeire, Severine and Xavier, Ramnik J and Weersma, Rinse K and Duerr, Richard H and Mathew, Christopher G and Rioux, John D and McGovern, Dermot P B and Cho, Judy H and Georges, Michel and Daly, Mark J and Barrett, Jeffrey C (2017) Fine-mapping inflammatory bowel disease loci to single-variant resolution. Nature, 547 (7662). pp. 173-178. ISSN 0028-0836
Gagliano, Sarah A. and Pouget, Jennie G. and Hardy, John and Knight, Jo and Barnes, Michael R. and Ryten, Mina and Weale, Mike (2016) Genomics implicates adaptive and innate immunity in Alzheimer’s and Parkinson’s diseases. Annals of Clinical and Translational Neurology, 3 (12). pp. 924-933.
Pouget, Jennie G. and Gonçalves, Vanessa F. and Spain, Sarah L. and Finucane, Hilary K. and Raychaudhuri, Soumya and Kennedy, James L. and Knight, Jo (2016) Genome-wide association studies suggest limited immune gene enrichment in schizophrenia compared to 5 autoimmune diseases. Schizophrenia Bulletin, 42 (5). pp. 1176-1184. ISSN 0586-7614
Mutsaerts, Henri J. M. M. and Knight, Jo (2016) CEREBRAL PERFUSION AS AN IMAGING BIOMARKER OF PRESYMPTOMATIC GENETIC FRONTOTEMPORAL DEMENTIA : PRELIMINARY RESULTS FROM THE GENETIC FRONTOTEMPORAL DEMENTIA INITIATIVE (GENFI). Alzheimer's and Dementia, 12 (7 Supp). P409-P411. ISSN 1552-5260
Masellis, Mario and Collinson, Shannon and Freeman, Natalie and Tampakeras, Maria and Levy, Joseph and Tchelet, Amir and Eyal, Eli and Berkovich, Elijahu and Eliaz, Rom E. and Abler, Victor and Grossman, Iris and Fitzer-Attas, Cheryl and Tiwari, Arun and Hayden, Michael R. and Kennedy, James L. and Lang, Anthony E. and Knight, Jo (2016) Dopamine D2 receptor gene variants and response to rasagiline in early Parkinson's disease : a pharmacogenetic study. Brain, 139 (7). pp. 2050-2062. ISSN 0006-8950
Prins, Bram P and Abbasi, Ali and Wong, Anson and Vaez, Ahmad and Nolte, Ilja and Franceschini, Nora and Stuart, Philip E and Guterriez Achury, Javier and Mistry, Vanisha and Bradfield, Jonathan P and Valdes, Ana M and Bras, Jose and Shatunov, Aleksey and Lu, Chen and Han, Buhm and Raychaudhuri, Soumya and Bevan, Steve and Mayes, Maureen D and Tsoi, Lam C and Evangelou, Evangelos and Nair, Rajan P and Grant, Struan F A and Polychronakos, Constantin and Radstake, Timothy R D and van Heel, David A and Dunstan, Melanie L and Wood, Nicholas W and Al-Chalabi, Ammar and Dehghan, Abbas and Hakonarson, Hakon and Markus, Hugh S and Elder, James T and Knight, Jo and Arking, Dan E and Spector, Timothy D and Koeleman, Bobby P C and van Duijn, Cornelia M and Martin, Javier and Morris, Andrew P and Weersma, Rinse K and Wijmenga, Cisca and Munroe, Patricia B and Perry, John R B and Pouget, Jennie G and Jamshidi, Yalda and Snieder, Harold and Alizadeh, Behrooz Z (2016) Investigating the causal relationship of C-reactive protein with 32 complex somatic and psychiatric outcomes : a large-scale cross-consortium Mendelian randomization study. PLoS Medicine, 13 (6): e1001976. ISSN 1549-1277
Patel, Sejal and Park, Min Tae M. and Chakravarty, M. Mallar and Knight, Jo (2016) Gene prioritization for imaging genetics studies using gene ontology and a stratified false discovery rate approach. Frontiers in Neuroinformatics, 10: 14. ISSN 1662-5196
Taylor, Danielle L. and Tiwari, Arun K. and Lieberman, Jeffrey A. and Potkin, Steven G. and Meltzer, Herbert Y. and Knight, Jo and Remington, Gary and Müller, Daniel J. and Kennedy, James L. (2016) Genetic association analysis of N-methyl-d-aspartate receptor subunit gene GRIN2B and clinical response to clozapine. Human Psychopharmacology: Clinical and Experimental, 31 (2). pp. 121-134. ISSN 0885-6222
Kevans, David and Silverberg, Mark S. and Borowski, Krzysztof and Griffiths, Anne and Xu, Wei and Onay, Venus and Paterson, Andrew D. and Knight, Jo and Croitoru, Ken (2016) IBD genetic risk profile in healthy first-degree relatives of Crohn's disease patients. Journal of Crohn's and Colitis, 10 (2). pp. 209-215. ISSN 1873-9946
Waterman, Matti and Knight, Jo and Dinani, Amreen and Xu, Wei and Stempak, Joanne M. and Croitoru, Kenneth and Nguyen, Geoffrey C. and Cohen, Zane and McLeod, Robin S. and Greenberg, Gordon R. and Steinhart, A. Hillary and Silverberg, Mark S. (2015) Predictors of outcome in ulcerative colitis. Inflammatory Bowel Diseases, 21 (9). pp. 2097-2105. ISSN 1078-0998
Gagliano, Sarah A. and Ravji, Reena and Barnes, Michael R. and Weale, Michael E. and Knight, Jo (2015) Smoking gun or circumstantial evidence? : comparison of statistical learning methods using functional annotations for prioritizing risk variants. Scientific Reports, 5: 13373. ISSN 2045-2322
Lobo, D. S. S. and Aleksandrova, L. and Knight, Jo and Casey, D. M. and el-Guebaly, N. and Nobrega, J. N. and Kennedy, J. L. (2015) Addiction-related genes in gambling disorders : new insights from parallel human and pre-clinical models. Molecular Psychiatry, 20 (8). pp. 1002-1010. ISSN 1359-4184
Zai, Clement C. and Gonçalves, Vanessa F. and Tiwari, Arun K. and Gagliano, Sarah A. and Hosang, Georgina and de Luca, Vincenzo and Shaikh, Sajid A. and King, Nicole and Chen, Qian and Xu, Wei and Strauss, John and Breen, Gerome and Lewis, Cathryn M. and Farmer, Anne E. and McGuffin, Peter and Knight, Jo and Vincent, John B. and Kennedy, James L. (2015) A genome-wide association study of suicide severity scores in bipolar disorder. Journal of Psychiatric Research, 65. pp. 23-29. ISSN 0022-3956
Gagliano, Sarah A. and Paterson, Andrew D. and Weale, Michael E. and Knight, Jo (2015) Assessing models for genetic prediction of complex traits : a comparison of visualization and quantitative methods. BMC Genomics, 16: 405. ISSN 1471-2164
Prescott, Natalie J. and Lehne, Benjamin and Stone, Kristina and Lee, James C. and Taylor, Kirstin and Knight, Jo and Papouli, Efterpi and Mirza, Muddassar M. and Simpson, Michael A. and Spain, Sarah L. and Lu, Grace and Fraternali, Franca and Bumpstead, Suzannah J. and Gray, Emma and Amar, Ariella and Bye, Hannah and Green, Peter and Chung-Faye, Guy and Hayee, Bu'Hussain and Pollok, Richard and Satsangi, Jack and Parkes, Miles and Barrett, Jeffrey C. and Mansfield, John C. and Sanderson, Jeremy and Lewis, Cathryn M. and Weale, Michael E. and Schlitt, Thomas and Mathew, Christopher G. (2015) Pooled sequencing of 531 genes in inflammatory bowel disease identifies an associated rare variant in BTNL2 and implicates other immune related genes. PLoS Genetics, 11 (2): e1004955. ISSN 1553-7390
Pouget, Jennie G. and Gonçalves, Vanessa F. and Nurmi, Erika L. and Laughlin, Christopher P. and Mallya, Karyn S. and McCracken, James T. and Aman, Michael G. and McDougle, Christopher J. and Scahill, Lawrence and Misener, Virginia L. and Tiwari, Arun K. and Zai, Clement C. and Brandl, Eva J. and Felsky, Daniel and Leung, Amy Q. and Lieberman, Jeffrey A. and Meltzer, Herbert Y. and Potkin, Steven G. and Niedling, Charlotte and Steimer, Werner and Leucht, Stefan and Knight, Jo and Müller, Daniel J. and Kennedy, James L. (2015) Investigation of TSPO variants in schizophrenia and antipsychotic treatment outcomes. Pharmacogenomics, 16 (1). pp. 5-22. ISSN 1462-2416
Knights, Dan and Silverberg, Mark S. and Weersma, Rinse K. and Gevers, Dirk and Dijkstra, Gerard and Huang, Hailiang and Tyler, Andrea D. and van Sommeren, Suzanne and Imhann, Floris and Stempak, Joanne M. and Huang, Hu and Vangay, Pajau and Al-Ghalith, Gabriel A. and Russell, Caitlin and Sauk, Jenny and Knight, Jo and Daly, Mark J. and Huttenhower, Curtis and Xavier, Ramnik J. (2014) Complex host genetics influence the microbiome in inflammatory bowel disease. Genome Biology, 6 (12): 107. ISSN 1465-6906
Gagliano, Sarah A. and Tiwari, Arun K. and Freeman, Natalie and Lieberman, Jeffrey A. and Meltzer, Herbert Y. and Kennedy, James L. and Knight, Jo and Müller, Daniel J. (2014) Protein kinase cAMP-dependent regulatory type II beta (PRKAR2B) gene variants in antipsychotic-induced weight gain. Human Psychopharmacology: Clinical and Experimental, 29 (4). pp. 330-335. ISSN 0885-6222
Navarini, Alexander A. and Simpson, Michael A. and Weale, Michael and Knight, Jo and Carlavan, Isabelle and Reiniche, Pascale and Burden, David A. and Layton, Alison and Bataille, Veronique and Allen, Michael and Pleass, Robert and Pink, Andrew and Creamer, Daniel and English, John and Munn, Stephanie and Walton, Shernaz and Willis, Carolyn and Déret, Sophie and Voegel, Johannes J. and Spector, Tim and Smith, Catherine H. and Trembath, Richard C. and Barker, Jonathan N. W. N. (2014) Genome-wide association study identifies three novel susceptibility loci for severe Acne vulgaris. Nature Communications, 5: 4020. ISSN 2041-1723
Gagliano, Sarah A. and Barnes, Michael R. and Weale, Michael E. and Knight, Jo (2014) A Bayesian method to incorporate hundreds of functional characteristics with association evidence to improve variant prioritization. PLoS ONE, 9 (5): e98122. ISSN 1932-6203
Xu, Wei and Cohen-Woods, Sarah and Chen, Qian and Noor, Abdul and Knight, Jo and Hosang, Georgina and Parikh, Sagar V. and De Luca, Vincenzo and Tozzi, Federica and Muglia, Pierandrea and Forte, Julia and McQuillin, Andrew and Hu, Pingzhao and Gurling, Hugh M. D. and Kennedy, James L. and McGuffin, Peter and Farmer, Anne and Strauss, John and Vincent, John B. (2014) Genome-wide association study of bipolar disorder in Canadian and UK populations corroborates disease loci including SYNE1 and CSMD1. Journal of Medical Genetics, 15: 2. ISSN 0022-2593
Knight, Jo and Spain, Sarah L. and Capon, Francesca and Hayday, Adrian and Nestle, Frank O. and Clop, Alex and Barker, Jonathan N. W. N. and Weale, Michael E. and Trembath, Richard C. (2012) Conditional analysis identifies three novel major histocompatibility complex loci associated with psoriasis. Human Molecular Genetics, 21 (23). pp. 5185-5192. ISSN 0964-6906
Tsoi, Lam C. and Spain, Sarah L. and Knight, Jo and Ellinghaus, Eva and Stuart, Philip E. and Capon, Francesca and Ding, Jun and Li, Yanming and Tejasvi, Trilokraj and Gudjonsson, Johann E. and Kang, Hyun M. and Allen, Michael H. and McManus, Ross and Novelli, Giuseppe and Samuelsson, Lena and Schalkwijk, Joost and Ståhle, Mona and Burden, A. David and Smith, Catherine H. and Cork, Michael J. and Estivill, Xavier and Bowcock, Anne M. and Krueger, Gerald G. and Weger, Wolfgang and Worthington, Jane and Tazi-Ahnini, Rachid and Nestle, Frank O. and Hayday, Adrian and Hoffmann, Per and Winkelmann, Juliane and Wijmenga, Cisca and Langford, Cordelia and Edkins, Sarah and Andrews, Robert and Blackburn, Hannah and Strange, Amy and Band, Gavin and Pearson, Richard D. and Vukcevic, Damjan and Spencer, Chris C. A. and Deloukas, Panos and Mrowietz, Ulrich and Schreiber, Stefan and Weidinger, Stephan and Koks, Sulev and Kingo, Külli and Esko, Tonu and Metspalu, Andres and Lim, Henry W. and Voorhees, John J. (2012) Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity. Nature Genetics, 44 (12). pp. 1341-1348. ISSN 1061-4036
Lewis, Cathryn M. and Knight, Jo (2012) Introduction to genetic association studies. Cold Spring Harbor Protocols, 2012 (3). pp. 297-306. ISSN 1940-3402
Onoufriadis, Alexandros and Simpson, Michael A. and Pink, Andrew E. and Di Meglio, Paola and Smith, Catherine H. and Pullabhatla, Venu and Knight, Jo and Spain, Sarah L. and Nestle, Frank O. and Burden, A. David and Capon, Francesca and Trembath, Richard C. and Barker, Jonathan N. W. N. (2011) Mutations in IL36RN/IL1F5 are associated with the severe episodic inflammatory skin disease known as generalized pustular psoriasis. American Journal of Human Genetics, 89 (3). pp. 432-437. ISSN 0002-9297
Breen, Gerome and Webb, Bradley Todd and Butler, Amy W. and van den Oord, Edwin J. C. G. and Tozzi, Federica and Craddock, Nick and Gill, Mike and Korszun, Ania and Maier, Wolfgang and Middleton, Lefkos and Mors, Ole and Owen, Michael J. and Cohen-Woods, Sarah and Perry, Julia and Galwey, Nicholas W. and Upmanyu, Ruchi and Craig, Ian and Lewis, Cathryn M. and Ng, Mandy and Brewster, Shyama and Preisig, Martin and Rietschel, Marcella and Jones, Lisa and Knight, Jo and Rice, John and Muglia, Pierandrea and Farmer, Anne E. and McGuffin, Peter (2011) A genome-wide significant linkage for severe depression on chromosome 3 : the depression network study. American Journal of Psychiatry, 168 (8). pp. 840-847. ISSN 0002-953X
Knight, Jo and Barnes, Michael R. and Breen, Gerome and Weale, Michael E. (2011) Using functional annotation for the empirical determination of Bayes Factors for genome-wide association study analysis. PLoS ONE, 6 (4): e14808. ISSN 1932-6203
van der Zanden, Loes F. M. and van Rooij, Iris A. L. M. and Feitz, Wout F. J. and Knight, Jo and Donders, A. Rogier T. and Renkema, Kirsten Y. and Bongers, Ernie M. H. F. and Vermeulen, Sita H. H. M. and Kiemeney, Lambertus A. L. M. and Veltman, Joris A. and Arias-Vásquez, Alejandro and Zhang, Xufeng and Markljung, Ellen and Qiao, Liang and Baskin, Laurence S. and Nordenskjöld, Agneta and Roeleveld, Nel and Franke, Barbara and Knoers, Nine V. A. M. (2011) Common variants in DGKK are strongly associated with risk of hypospadias. Nature Genetics, 43 (1). pp. 48-50. ISSN 1061-4036
Strange, Amy and Capon, Francesca and Spencer, Chris C. A. and Knight, Jo and Weale, Michael E. and Allen, Michael H. and Barton, Anne and Band, Gavin and Bellenguez, Céline and Bergboer, Judith G M and Blackwell, Jenefer M and Bramon, Elvira and Bumpstead, Suzannah J and Casas, Juan P and Cork, Michael J and Corvin, Aiden and Deloukas, Panos and Dilthey, Alexander and Duncanson, Audrey and Edkins, Sarah and Estivill, Xavier and Fitzgerald, Oliver and Freeman, Colin and Giardina, Emiliano and Gray, Emma and Hofer, Angelika and Hüffmeier, Ulrike and Hunt, Sarah E and Irvine, Alan D and Jankowski, Janusz and Kirby, Brian and Langford, Cordelia and Lascorz, Jesús and Leman, Joyce and Leslie, Stephen and Mallbris, Lotus and Markus, Hugh S and Mathew, Christopher G and McLean, W H Irwin and McManus, Ross and Mössner, Rotraut and Moutsianas, Loukas and Naluai, Asa T and Nestle, Frank O and Novelli, Giuseppe and Onoufriadis, Alexandros and Palmer, Colin N A and Perricone, Carlo and Pirinen, Matti and Plomin, Robert (2010) A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. Nature Genetics, 42 (11). pp. 985-990. ISSN 1061-4036
Cohen-Woods, Sarah and Craig, Ian and Gaysina, Darya and Gray, Joanna and Gunasinghe, Cerisse and Craddock, Nick and Elkin, Amanda and Jones, Lisa and Kennedy, James and King, Nicole and Korszun, Ania and Knight, Jo and Owen, Michael and Parikh, Sagar and Strauss, John and Sterne, Abram and Tozzi, Federica and Perry, Julia and Muglia, Pierandrea and Vincent, John and McGuffin, Peter and Farmer, Anne (2010) The Bipolar Association Case-Control Study (BACCS) and meta-analysis : no association with the 5,10-Methylenetetrahydrofolate reductase gene and bipolar disorder. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 153B (7). pp. 1298-1304. ISSN 1552-4841
Knight, Jo and Rochberg, Nanette S. and Saccone, Scott F. and Nurnberger, John I. and Rice, John P. (2010) An investigation of candidate regions for association with bipolar disorder. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 153B (7). pp. 1292-1297. ISSN 1552-4841
Beall, Cynthia M. and Cavalleri, Gianpiero L. and Deng, Libin and Elston, Robert C. and Gao, Yang and Knight, Jo and Li, Chaohua and Li, Jiang Chuan and Liang, Yu and McCormack, Mark and Montgomery, Hugh E. and Pan, Hao and Robbins, Peter A. and Shianna, Kevin V. and Tam, Siu Cheung and Tsering, Ngodrop and Veeramah, Krishna R. and Wang, Wei and Wangdui, Puchung and Weale, Michael E. and Xu, Yaomin and Xu, Zhe and Yang, Ling and Zaman, M. Justin and Zeng, Changqing and Zhang, Li and Zhang, Xianglong and Zhaxi, Pingcuo and Zheng, Yong Tang (2010) Natural selection on EPAS1 (HIF2alpha) associated with low hemoglobin concentration in Tibetan highlanders. Proceedings of the National Academy of Sciences of the United States of America, 107 (25). pp. 11459-11464. ISSN 0027-8424
Campbell, Desmond D. and Sham, Pak C. and Knight, Jo and Wickham, Harvey and Landau, Sabine (2010) Software for generating liability distributions for pedigrees conditional on their observed disease states and covariates. Genetic Epidemiology, 34 (2). pp. 159-170. ISSN 0741-0395
Cohen-Woods, Sarah and Gaysina, Daria and Craddock, Nick and Farmer, Anne and Gray, Joanna and Gunasinghe, Cerisse and Hoda, Farzana and Jones, Lisa and Knight, Jo and Korszun, Ania and Owen, Michael J. and Sterne, Abram and Craig, Ian W. and McGuffin, Peter (2009) Depression Case Control (DeCC) study fails to support involvement of the muscarinic acetylcholine receptor M2 (CHRM2) gene in recurrent major depressive disorder. Human Molecular Genetics, 18 (8). pp. 1504-1509. ISSN 0964-6906
Knight, Jo and Saccone, Scott F. and Zhang, Zhehao and Ballinger, Dennis G. and Rice, John P. (2009) A comparison of association statistics between pooled and individual genotypes. Human Heredity, 67 (4). pp. 219-225. ISSN 0001-5652
Chen, Wai and Zhou, Kaixin and Sham, Pak and Franke, Barbara and Kuntsi, Jonna and Campbell, Desmond and Fleischman, Karin and Knight, Jo and Andreou, Penny and Arnold, Renée and Altink, Marieke and Boer, Frits and Boholst, Mary Jane and Buschgens, Cathelijne and Butler, Louise and Christiansen, Hanna and Fliers, Ellen and Howe-Forbes, Raoul and Gabriëls, Isabel and Heise, Alexander and Korn-Lubetzki, Isabelle and Marco, Rafaela and Medad, She'era and Minderaa, Ruud and Müller, Ueli C and Mulligan, Aisling and Psychogiou, Lamprini and Rommelse, Nanda and Sethna, Vaheshta and Uebel, Henrik and McGuffin, Peter and Plomin, Robert and Banaschewski, Tobias and Buitelaar, Jan and Ebstein, Richard and Eisenberg, Jacques and Gill, Michael and Manor, Iris and Miranda, Ana and Mulas, Fernando and Oades, Robert D. and Roeyers, Herbert and Rothenberger, Aribert and Sergeant, Joseph and Sonuga-Barke, Edmund and Steinhausen, Hans-Christoph and Taylor, Eric and Thompson, Margaret and Faraone, Stephen V. and Asherson, Philip (2008) DSM-IV combined type ADHD shows familial association with sibling trait scores : a sampling strategy for QTL linkage. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 147B (8). pp. 1450-1460. ISSN 1552-4841
Curtis, David and Vine, Anna E. and Knight, Jo (2008) A simple method for assessing the strength of evidence for association at the level of the whole gene. Advances and Applications in Bioinformatics and Chemistry : AABC, 1. pp. 115-120. ISSN 1178-6949
Knight, Jo and Curtis, David and Sham, Pak C. (2008) CLUMPHAP : a simple tool for performing haplotype-based association analysis. Genetic Epidemiology, 32 (6). pp. 539-545. ISSN 0741-0395
Curtis, D. and Vine, A. E. and Knight, Jo (2008) Investigation into the ability of SNP chipsets and microsatellites to detect association with a disease locus. Annals of Human Genetics, 72 (4). pp. 547-556. ISSN 0003-4800
Curtis, D. and Vine, A. E. and Knight, Jo (2008) Study of regions of extended homozygosity provides a powerful method to explore haplotype structure of human populations. Annals of Human Genetics, 72 (2). pp. 261-278. ISSN 0003-4800
O'Gara, Colin and Knight, Jo and Stapleton, John and Luty, Jason and Neale, Ben and Nash, Matt and Heuzo-Diaz, Patricia and Hoda, Farzana and Cohen, Sarah and Sutherland, Gay and Collier, David and Sham, Pak and Ball, David and McGuffin, Peter and Craig, Ian (2008) Association of the serotonin transporter gene, neuroticism and smoking behaviours. Journal of Human Genetics, 53 (3). pp. 239-246. ISSN 1435-232X
Vermeulen, S. H. H. M. and Den Heijer, M. and Sham, Pak C. and Knight, Jo (2007) Application of multi-locus analytical methods to identify interacting loci in case-control studies. Annals of Human Genetics, 71 (5). pp. 689-700. ISSN 0003-4800
Curtis, David and Vine, Anna E. and Knight, Jo (2007) A pragmatic suggestion for dealing with results for candidate genes obtained from genome wide association studies. Genetics, 8: 20. ISSN 0016-6731
McGuffin, Peter and Cohen, Sarah and Knight, Jo (2007) Homing in on depression genes. American Journal of Psychiatry, 164 (2). pp. 195-197. ISSN 0002-953X
North, Bernard V. and Sham, Pak C. and Knight, Jo and Martin, E. R. and Curtis, David (2006) Investigation of the ability of haplotype association and logistic regression to identify associated susceptibility loci. Annals of Human Genetics, 70 (6). pp. 893-906. ISSN 0003-4800
Brookes, K. and Xu, X. and Chen, W. and Zhou, Kaixin and Neale, Ben and Lowe, N. and Anney, R. and Franke, B. and Gill, M. and Ebstein, Richard and Buitelaar, Jan and Sham, P and Campbell, D. and Knight, Jo and Andreou, Penny and Altink, Marieke and Arnold, R. and Boer, F and Buschgens, C and Butler, L and Christiansen, H and Feldman, L and Fleischman, K and Fliers, E and Howe-Forbes, R and Goldfarb, A and Heise, A and Gabriëls, I and Korn-Lubetzki, I and Johansson, L and Marco, R and Medad, S and Minderaa, R and Mulas, F and Müller, U and Mulligan, A and Rabin, K and Rommelse, N and Sethna, V and Sorohan, J and Uebel, H and Psychogiou, L and Weeks, A and Barrett, R and Craig, I and Banaschewski, T and Sonuga-Barke, E and Eisenberg, J and Kuntsi, J and Manor, I and McGuffin, P and Miranda, A and Oades, R D and Plomin, R and Roeyers, H and Rothenberger, A and Sergeant, J and Steinhausen, H-C and Taylor, E and Thompson, M and Faraone, S V and Asherson, P (2006) The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder : association signals in DRD4, DAT1 and 16 other genes. Molecular Psychiatry, 11 (10). pp. 934-953. ISSN 1359-4184
Knight, Jo and Sham, Pak (2006) Design and analysis of association studies using pooled DNA from large twin samples. Behavior Genetics, 36 (5). pp. 665-677. ISSN 0001-8244
Nibali, L. and Parkar, M. and Brett, P. and Knight, Jo and Tonetti, M. S. and Griffiths, G. S. (2006) NADPH oxidase (CYBA) and FcgammaR polymorphisms as risk factors for aggressive periodontitis : a case-control association study. Journal of Clinical Periodontology, 33 (8). pp. 529-539. ISSN 0303-6979
Hamilton, Gillian and Samedi, Farzana and Knight, Jo and Archer, Nicola and Foy, Catherine and Walter, Sarah and Turic, Dragana and Jehu, Luke and Moore, Pamela and Hollingworth, Paul and O'Donovan, Michael C. and Williams, Julie and Owen, Michael J. and Lovestone, Simon and Powell, John F. (2006) Polymorphisms in the phosphate and tensin homolog gene are not associated with late-onset Alzheimer's disease. Neuroscience Letters, 401 (1-2). pp. 77-80. ISSN 0304-3940
Curtis, David and Knight, Jo and Sham, Pak C. (2006) Program report : GENECOUNTING support programs. Annals of Human Genetics, 70 (Pt 2). pp. 277-279. ISSN 0003-4800
Brookes, Keeley-Joanne and Mill, Jon and Guindalini, Camilla and Curran, Sarah and Xu, Xiaohui and Knight, Jo and Chen, Chih-Ken and Huang, Yu-Shu and Sethna, Vaheshta and Taylor, Eric and Chen, Wai and Breen, Gerome and Asherson, Philip (2006) A common haplotype of the dopamine transporter gene associated with attention-deficit/hyperactivity disorder and interacting with maternal use of alcohol during pregnancy. Archives of General Psychiatry, 63 (1). pp. 74-81. ISSN 0003-990X
McGuffin, Peter and Knight, Jo and Breen, Gerome and Brewster, Shyama and Boyd, Peter R. and Craddock, Nick and Gill, Mike and Korszun, Ania and Maier, Wolfgang and Middleton, Lefkos and Mors, Ole and Owen, Michael J. and Perry, Julia and Preisig, Martin and Reich, Theodore and Rice, John and Rietschel, Marcella and Jones, Lisa and Sham, Pak and Farmer, Anne E. (2005) Whole genome linkage scan of recurrent depressive disorder from the depression network study. Human Molecular Genetics, 14 (22). pp. 3337-3345. ISSN 0964-6906
Curtis, David and Knight, Jo and Sham, Pak C. (2005) A new method of linkage analysis using LOD scores for quantitative traits supports linkage of monoamine oxidase activity to D17S250 in the Collaborative Study on the Genetics of Alcoholism pedigrees. Psychiatric Genetics, 15 (3). pp. 181-187. ISSN 0955-8829
Butcher, Lee M. and Meaburn, Emma and Knight, Jo and Sham, Pak C. and Schalkwyk, Leonard C. and Craig, Ian W. and Plomin, Robert (2005) SNPs, microarrays and pooled DNA : identification of four loci associated with mild mental impairment in a sample of 6000 children. Human Molecular Genetics, 14 (10). pp. 1315-1325. ISSN 0964-6906
Xu, Xiaohui and Knight, Jo and Brookes, Keeley and Mill, Jonathan and Sham, Pak and Craig, Ian and Taylor, Eric and Asherson, Philip (2005) DNA pooling analysis of 21 norepinephrine transporter gene SNPs with attention deficit hyperactivity disorder : no evidence for association. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 134B (1). pp. 115-118. ISSN 1552-4841
Mill, Jonathan and Xu, Xiaohui and Ronald, Angelica and Curran, Sarah and Price, Tom and Knight, Jo and Craig, Ian and Sham, Pak and Plomin, Robert and Asherson, Philip (2005) Quantitative trait locus analysis of candidate gene alleles associated with attention deficit hyperactivity disorder (ADHD) in five genes : DRD4, DAT1, DRD5, SNAP-25, and 5HT1B. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 133B (1). pp. 68-73. ISSN 1552-4841
Mill, J. and Richards, S. and Knight, Jo and Curran, S. and Taylor, Eleanor and Asherson, Philip (2004) Haplotype analysis of SNAP-25 suggests a role in the aetiology of ADHD. Molecular Psychiatry, 9 (8). pp. 801-810. ISSN 1359-4184
Asherson, Philip and Knight, Jo (2004) Attention-Deficit Hyperactivity Disorder in the post-genomic era. European Child and Adolescent Psychiatry, 13 (Suppl ). I50-70. ISSN 1018-8827
Knight, Jo (2004) A survey of current software for genetic power calculations. BMC Genomics, 1 (3). pp. 225-227. ISSN 1473-9542
Hassan, A. E. M. and Gormley, K. and O'Sullivan, Michael and Knight, Jo and Sham, Pak C. and Vallance, P. and Bamford, J. and Markus, Hugh S. (2004) Endothelial nitric oxide gene haplotypes and risk of cerebral small-vessel disease. Stroke; a journal of cerebral circulation, 35 (3). pp. 654-659. ISSN 0039-2499
Sham, Pak C. and Rijsdijk, F. V. and Knight, Jo and Makoff, Andrew and North, B. and Curtis, D. (2004) Haplotype association analysis of discrete and continuous traits using mixture of regression models. Behavior Genetics, 34 (2). pp. 207-214. ISSN 0001-8244
Knight, Jo and North, Bernard V. and Sham, Pak C. and Curtis, David (2003) Mapping loci influencing blood pressure in the Framingham pedigrees using model-free LOD score analysis of a quantitative trait. Genetics, 4 (Suppl.): S74. ISSN 0016-6731
Knight, Jo and Munroe, P. B. and Pembroke, J. C. and Caulfield, M. J. (2003) Human chromosome 17 in essential hypertension. Annals of Human Genetics, 67 (2). pp. 193-206. ISSN 0003-4800
Chioza, Barry and Osei-Lah, Abena and Nashef, Lina and Suarez-Merino, Blanca and Wilkie, Hazel and Sham, Pak and Knight, Jo and Asherson, Philip and Makoff, Andrew J (2002) Haplotype and linkage disequilibrium analysis to characterise a region in the calcium channel gene CACNA1A associated with idiopathic generalised epilepsy. European Journal of Human Genetics, 10 (12). pp. 857-864. ISSN 1018-4813
Knight, Jo and Gardner, G. T. and Clark, A. J. and Caulfield, M. J. (2000) Investigation of chromosome 17q as a locus for human essential hypertension in African Caribbeans. Journal of Human Hypertension, 14 (6). pp. 385-387. ISSN 0950-9240
Munroe, P. B. and Knight, Jo and Caulfield, M. J. (2000) 1990-2000 : progress in determining high blood pressure genes. Annals of the Academy of Medicine, Singapore, 29 (3). pp. 357-363. ISSN 0304-4602
Contribution in Book/Report/Proceedings
El-Haj, Mahmoud and Rutherford, Nathan and Coole, Matthew and Ezeani, Ignatius and Prentice, Sheryl and Ide, Nancy and Knight, Jo and Piao, Scott and Mariani, John and Rayson, Paul and Suderman, Keith (2020) Infrastructure for Semantic Annotation in the Genomics Domain. In: LREC 2020, Twelfth International Conference on Language Resources and Evaluation : LREC'20. European Language Resources Association (ELRA), Paris, pp. 6921-6929. ISBN 9791095546344
El Haj, Mahmoud and Rayson, Paul Edward and Piao, Scott Songlin and Knight, Jo (2018) Profiling Medical Journal Articles Using a Gene Ontology Semantic Tagger. In: LREC 2018, Eleventh International Conference on Language Resources and Evaluation :. European Language Resources Association (ELRA), JPN, pp. 4593-4597. ISBN 9791095546009
Knight, Jo and Sham, Pak and Shaun, Purcell and Neale, Ben (2007) Regional multi-locus association models. In: Statistical genetics : gene mapping through linkage and association. Taylor and Francis, London. ISBN 9780415410403
Caulfield, Mark and Knight, Jo and Gardener, G. and O’Shea, S. and Monroe, P. (2002) Genes for hypertension. In: An introduction to vascular biology : from basic science to clinical practice. Cambridge University Press, Cambridge. ISBN 9780521796521
Monograph
Russell, Siân and Stocker, Rachel and Cockshott, Zoë and Mason, Suzanne and Knight, Jo and Hanratty, Barbara and Preston, Nancy (2023) Use of a digital application to enhance communication and triage between care homes and National Health Service community services in the United Kingdom : a qualitative evaluation. Other. medRxiv.
Contribution to Conference
Mountain, Rachael and Knight, Jo and Haslam, Patrick and Gatheral, Timothy (2023) Measuring Diagnostic Quality : The Capacity of Electronic Health Records and the Role of Integrated Care Initiatives. In: Health Services Research UK Conference 2023, 2023-07-04 - 2023-07-06. (Unpublished)
Mountain, Rachael and Knight, Jo and Heys, Kelly and Giorgi, Emanuele and Gatheral, Timothy (2022) Spatio-temporal modelling of referrals to outpatient respiratory clinics in the integrated care system of the Morecambe Bay area. In: HSR UK Conference 2022, 2022-07-05 - 2022-07-07.
El-Haj, Mahmoud and Piao, Scott Songlin and Rayson, Paul Edward and Knight, Jo (2017) A Comparison Between Genetics Papers Relating to Immune Disorders and Psychiatric Disorders. In: UNSPECIFIED.