Zobrazeno 1 - 10
of 263
pro vyhledávání: '"David L Duffy"'
Autor:
Jenna E Rayner, David L Duffy, Darren J Smit, Kasturee Jagirdar, Katie J Lee, Brian De'Ambrosis, B Mark Smithers, Erin K McMeniman, Aideen M McInerney-Leo, Helmut Schaider, Mitchell S Stark, H Peter Soyer, Richard A Sturm
Publikováno v:
PLoS ONE, Vol 15, Iss 9, p e0238529 (2020)
Amelanotic/hypomelanotic melanoma is a clinicopathologic subtype with absent or minimal melanin. This study assessed previously reported coding variants in albinism genes (TYR, OCA2, TYRP1, SLC45A2, SLC24A5, LRMDA) and common intronic, regulatory var
Externí odkaz:
https://doaj.org/article/62e16674d71849ccb041bfc6a1b76bc0
Autor:
Seamus R McWhirter, David L Duffy, Katie J Lee, Glen Wimberley, Philip McClenahan, Natalie Ling, Marco Ardigo, Helmut Schaider, H Peter Soyer, Richard A Sturm
Publikováno v:
PLoS ONE, Vol 12, Iss 10, p e0186647 (2017)
Changes in dermoscopic patterns of naevi may be associated with melanoma; however, there is no consensus on which dermoscopic classification system is optimal. To determine whether different classification systems give comparable results and can be c
Externí odkaz:
https://doaj.org/article/f1084ada60284706b26c26bb5f387b74
Autor:
Baptiste Couvy-Duchesne, Jane L Ebejer, Nathan A Gillespie, David L Duffy, Ian B Hickie, Paul M Thompson, Nicholas G Martin, Greig I de Zubicaray, Katie L McMahon, Sarah E Medland, Margaret J Wright
Publikováno v:
PLoS ONE, Vol 11, Iss 1, p e0146271 (2016)
Head motion (HM) is a well known confound in analyses of functional MRI (fMRI) data. Neuroimaging researchers therefore typically treat HM as a nuisance covariate in their analyses. Even so, it is possible that HM shares a common genetic influence wi
Externí odkaz:
https://doaj.org/article/d0efcbca87144cd2a997b77d727fbd47
Autor:
Adaikalavan Ramasamy, Mikko Kuokkanen, Sailaja Vedantam, Zofia K Gajdos, Alexessander Couto Alves, Helen N Lyon, Manuel A R Ferreira, David P Strachan, Jing Hua Zhao, Michael J Abramson, Matthew A Brown, Lachlan Coin, Shyamali C Dharmage, David L Duffy, Tari Haahtela, Andrew C Heath, Christer Janson, Mika Kähönen, Kay-Tee Khaw, Jaana Laitinen, Peter Le Souef, Terho Lehtimäki, Australian Asthma Genetics Consortium collaborators, Pamela A F Madden, Guy B Marks, Nicholas G Martin, Melanie C Matheson, Cameron D Palmer, Aarno Palotie, Anneli Pouta, Colin F Robertson, Jorma Viikari, Elisabeth Widen, Matthias Wjst, Deborah L Jarvis, Grant W Montgomery, Philip J Thompson, Nick Wareham, Johan Eriksson, Pekka Jousilahti, Tarja Laitinen, Juha Pekkanen, Olli T Raitakari, George T O'Connor, Veikko Salomaa, Marjo-Riitta Jarvelin, Joel N Hirschhorn
Publikováno v:
PLoS ONE, Vol 8, Iss 3 (2013)
[This corrects the article DOI: 10.1371/journal.pone.0044008.].
Externí odkaz:
https://doaj.org/article/731bc0c9a5f74d86b5e0ca5199bfcf97
Autor:
Jane L Ebejer, Sarah E Medland, Julius van der Werf, Cedric Gondro, Anjali K Henders, Michael Lynskey, Nicholas G Martin, David L Duffy
Publikováno v:
PLoS ONE, Vol 7, Iss 10, p e47404 (2012)
BackgroundThe Prevalence and persistence of ADHD have not been described in young Australian adults and few studies have examined how conduct problems (CP) are associated with ADHD for this age group. We estimate lifetime and adult prevalence and per
Externí odkaz:
https://doaj.org/article/a5f86b5be4a64f1daa296e09b4f3851a
Autor:
Adaikalavan Ramasamy, Mikko Kuokkanen, Sailaja Vedantam, Zofia K Gajdos, Alexessander Couto Alves, Helen N Lyon, Manuel A R Ferreira, David P Strachan, Jing Hua Zhao, Michael J Abramson, Matthew A Brown, Lachlan Coin, Shyamali C Dharmage, David L Duffy, Tari Haahtela, Andrew C Heath, Christer Janson, Mika Kähönen, Kay-Tee Khaw, Jaana Laitinen, Peter Le Souef, Terho Lehtimäki, Australian Asthma Genetics Consortium Collaborators, Pamela A F Madden, Guy B Marks, Nicholas G Martin, Melanie C Matheson, Cameron D Palmer, Aarno Palotie, Anneli Pouta, Colin F Robertson, Jorma Viikari, Elisabeth Widen, Matthias Wjst, Deborah L Jarvis, Grant W Montgomery, Philip J Thompson, Nick Wareham, Johan Eriksson, Pekka Jousilahti, Tarja Laitinen, Juha Pekkanen, Olli T Raitakari, George T O'Connor, Veikko Salomaa, Marjo-Riitta Jarvelin, Joel N Hirschhorn
Publikováno v:
PLoS ONE, Vol 7, Iss 9, p e44008 (2012)
Asthma has substantial morbidity and mortality and a strong genetic component, but identification of genetic risk factors is limited by availability of suitable studies.To test if population-based cohorts with self-reported physician-diagnosed asthma
Externí odkaz:
https://doaj.org/article/c816652d63b14f159aa85ccbfad1b788
Publikováno v:
PLoS ONE, Vol 6, Iss 7, p e22455 (2011)
Polycystic Kidney Disease is an autosomal dominant disease common in some lines of Bull Terriers (BTPKD). The disease is linked to the canine orthologue of human PKD1 gene, Pkd1, located on CFA06, but no disease-associated mutation has been reported.
Externí odkaz:
https://doaj.org/article/c6b510726b454860a801bf3fb0b1f58c
Autor:
Sharon E Johnatty, Jonathan Beesley, Xiaoqing Chen, Stuart Macgregor, David L Duffy, Amanda B Spurdle, Anna deFazio, Natalie Gava, Penelope M Webb, Mary Anne Rossing, Jennifer Anne Doherty, Marc T Goodman, Galina Lurie, Pamela J Thompson, Lynne R Wilkens, Roberta B Ness, Kirsten B Moysich, Jenny Chang-Claude, Shan Wang-Gohrke, Daniel W Cramer, Kathryn L Terry, Susan E Hankinson, Shelley S Tworoger, Montserrat Garcia-Closas, Hannah Yang, Jolanta Lissowska, Stephen J Chanock, Paul D Pharoah, Honglin Song, Alice S Whitemore, Celeste L Pearce, Daniel O Stram, Anna H Wu, Malcolm C Pike, Simon A Gayther, Susan J Ramus, Usha Menon, Aleksandra Gentry-Maharaj, Hoda Anton-Culver, Argyrios Ziogas, Estrid Hogdall, Susanne K Kjaer, Claus Hogdall, Andrew Berchuck, Joellen M Schildkraut, Edwin S Iversen, Patricia G Moorman, Catherine M Phelan, Thomas A Sellers, Julie M Cunningham, Robert A Vierkant, David N Rider, Ellen L Goode, Izhak Haviv, Georgia Chenevix-Trench, Ovarian Cancer Association Consortium, Australian Ovarian Cancer Study Group, Australian Cancer Study (Ovarian Cancer)
Publikováno v:
PLoS Genetics, Vol 6, Iss 7, p e1001016 (2010)
We hypothesized that variants in genes expressed as a consequence of interactions between ovarian cancer cells and the host micro-environment could contribute to cancer susceptibility. We therefore used a two-stage approach to evaluate common single
Externí odkaz:
https://doaj.org/article/8150099c1d344257b3e76549737867cc
Autor:
Fan Liu, Andreas Wollstein, Pirro G Hysi, Georgina A Ankra-Badu, Timothy D Spector, Daniel Park, Gu Zhu, Mats Larsson, David L Duffy, Grant W Montgomery, David A Mackey, Susan Walsh, Oscar Lao, Albert Hofman, Fernando Rivadeneira, Johannes R Vingerling, André G Uitterlinden, Nicholas G Martin, Christopher J Hammond, Manfred Kayser
Publikováno v:
PLoS Genetics, Vol 6, Iss 5, p e1000934 (2010)
Previous studies have successfully identified genetic variants in several genes associated with human iris (eye) color; however, they all used simplified categorical trait information. Here, we quantified continuous eye color variation into hue and s
Externí odkaz:
https://doaj.org/article/b85c848700bb4dc0baa52649358b5b5d
Autor:
Jiali Han, Peter Kraft, Hongmei Nan, Qun Guo, Constance Chen, Abrar Qureshi, Susan E Hankinson, Frank B Hu, David L Duffy, Zhen Zhen Zhao, Nicholas G Martin, Grant W Montgomery, Nicholas K Hayward, Gilles Thomas, Robert N Hoover, Stephen Chanock, David J Hunter
Publikováno v:
PLoS Genetics, Vol 4, Iss 5, p e1000074 (2008)
We conducted a multi-stage genome-wide association study of natural hair color in more than 10,000 men and women of European ancestry from the United States and Australia. An initial analysis of 528,173 single nucleotide polymorphisms (SNPs) genotype
Externí odkaz:
https://doaj.org/article/fe609731cf184438a653617acee222a4