Matthew H. Law

Alıntı yapanlar

	Hepsi	2020 yılından bugüne
Alıntılar	6243	4507
h-endeksi	41	35
i10-endeksi	79	73

1300

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975

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Genel erişim

Tümünü görüntüle

101 makale

3 makale

genel erişime açık olanlar

genel erişime açık olmayanlar

Finansman sağlayan kuruluşun getirdiği zorunluluğa dayalı olarak

Katkıda bulunan yazarlar

Stuart MacGregorProfessor, Statistical Genetics, QIMR Berghofer Medical Research Institute, Brisbane, Australiaqimr.edu.au üzerinde doğrulanmış e-posta adresine sahip
David C. WhitemanNHMRC Leadership Fellow, QIMR Berghofer Medical Research Instituteqimrberghofer.edu.au üzerinde doğrulanmış e-posta adresine sahip
Jue-Sheng OngQIMR Berghofer Medical Research Instituteqimrberghofer.edu.au üzerinde doğrulanmış e-posta adresine sahip
Catherine OlsenQIMR Berghofer Medical Research Instituteqimrberghofer.edu.au üzerinde doğrulanmış e-posta adresine sahip
Rachel NealeQIMR Berghofer Medical Research Instituteqimrberghofer.edu.au üzerinde doğrulanmış e-posta adresine sahip
Mark IlesLecturer, University of Leedsleeds.ac.uk üzerinde doğrulanmış e-posta adresine sahip
Puya GharahkhaniAssociate Professor, Statistical Genetics, QIMR Berghofer Medical Research Instituteqimrberghofer.edu.au üzerinde doğrulanmış e-posta adresine sahip
Anne CustThe Daffodil Centre and Melanoma Institute Australia, The University of Sydneysydney.edu.au üzerinde doğrulanmış e-posta adresine sahip
Graham MannCollege of Health and Medicine, Australian National Universityanu.edu.au üzerinde doğrulanmış e-posta adresine sahip
Jiyuan AnQueensland University of Technologyqut.edu.au üzerinde doğrulanmış e-posta adresine sahip
nicholas HAYWARDQIMR BERGHOFERQIMRBERGHOFER.EDU.AU üzerinde doğrulanmış e-posta adresine sahip
Grant MontgomeryProfessorial Research Fellow, Institute for Molecular Bioscience, The University of Queenslanduq.edu.au üzerinde doğrulanmış e-posta adresine sahip
D. Timothy BishopProfessor of Epidemiology, University of Leedsleeds.ac.uk üzerinde doğrulanmış e-posta adresine sahip
Mathias SeviiriStatistical Genetics Lab, QIMR Berghofer Medical Research Instituteqimrberghofer.edu.au üzerinde doğrulanmış e-posta adresine sahip
Nick MartinQIMR Berghofer Medical Research Instituteqimrberghofer.edu.au üzerinde doğrulanmış e-posta adresine sahip
Amelia SmitThe Daffodil Centre, a joint venture between Cancer Council NSW and the University of Sydneysydney.edu.au üzerinde doğrulanmış e-posta adresine sahip
Kevin M. BrownNational Cancer Institute, National Institutes of Healthnih.gov üzerinde doğrulanmış e-posta adresine sahip
Adele C GreenProfessor of Cancer Epidemiology, Queensland Institute of Medical Researchqimrberghofer.edu.au üzerinde doğrulanmış e-posta adresine sahip
Peter KanetskyMoffitt Cancer Center and Research Institutemoffitt.org üzerinde doğrulanmış e-posta adresine sahip
Upekha E. LiyanageQIMR Berghofer Medical Research Instituteqimrberghofer.edu.au üzerinde doğrulanmış e-posta adresine sahip

Takip et

Matthew H. Law

QIMR Berghofer Medical Research Institute

qimrberghofer.edu.au üzerinde doğrulanmış e-posta adresine sahip - Ana Sayfa

Statistical genetics cancer genetics complex disease genetics gene mapping


Başlık Alıntılara göre sırala Yıla göre sırala Başlığa göre sırala	Alıntı yapanlar Alıntı yapanlar	Yıl
A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma S Yokoyama, SL Woods, GM Boyle, LG Aoude, S MacGregor, V Zismann, ... Nature 480 (7375), 99-103, 2011	584	2011
Association between telomere length and risk of cancer and non-neoplastic diseases: a Mendelian randomization study PC Haycock, S Burgess, A Nounu, J Zheng, GN Okoli, J Bowden, ... JAMA oncology 3 (5), 636-651, 2017	569	2017
Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease W Zhou, M Kanai, KHH Wu, H Rasheed, K Tsuo, JB Hirbo, Y Wang, ... Cell Genomics 2 (10), 2022	299	2022
Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression JE Craig, X Han, A Qassim, M Hassall, JN Cooke Bailey, TG Kinzy, ... Nature genetics 52 (2), 160-166, 2020	276	2020
Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma MH Law, DT Bishop, JE Lee, M Brossard, NG Martin, EK Moses, F Song, ... Nature genetics 47 (9), 987, 2015	267	2015
Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucoma P Gharahkhani, KP Burdon, R Fogarty, S Sharma, AW Hewitt, S Martin, ... Nature genetics 46 (10), 1120-1125, 2014	237	2014
Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility MT Landi, DT Bishop, S MacGregor, MJ Machiela, AJ Stratigos, P Ghiorzo, ... Nature Genetics 52 (5), 494-504, 2020	202	2020
Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma S MacGregor, JS Ong, J An, X Han, T Zhou, OM Siggs, MH Law, ... Nature genetics 50 (8), 1067-1071, 2018	196	2018
The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions N Rahmioglu, S Mortlock, M Ghiasi, PL Møller, L Stefansdottir, ... Nature Genetics 55 (3), 423-436, 2023	159	2023
A variant in FTO shows association with melanoma risk not due to BMI MM Iles, MH Law, SN Stacey, J Han, S Fang, R Pfeiffer, M Harland, ... Nature genetics 45 (4), 428, 2013	145	2013
The effect on melanoma risk of genes previously associated with telomere length MM Iles, DT Bishop, JC Taylor, NK Hayward, M Brossard, AE Cust, ... Journal of the National Cancer Institute 106 (10), dju267, 2014	136	2014
Multitrait genetic association analysis identifies 50 new risk loci for gastro-oesophageal reflux, seven new loci for Barrett’s oesophagus and provides insights into clinical … JS Ong, J An, X Han, MH Law, P Nandakumar, J Schumacher, I Gockel, ... Gut 71 (6), 1053-1061, 2022	128	2022
Assessment of polygenic architecture and risk prediction based on common variants across fourteen cancers YD Zhang, AN Hurson, H Zhang, PP Choudhury, DF Easton, RL Milne, ... Nature communications 11 (1), 1-13, 2020	127	2020
Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: a Mendelian randomisation analysis Interleukin 1 Genetics Consortium The Lancet Diabetes & Endocrinology 3 (4), 243-253, 2015	122	2015
Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways DL Duffy, G Zhu, X Li, M Sanna, MM Iles, LC Jacobs, DM Evans, ... Nature communications 9 (1), 1-10, 2018	119	2018
Melanoma genetics: recent findings take us beyond well-traveled pathways MH Law, S MacGregor, NK Hayward Journal of Investigative Dermatology 132 (7), 1763-1774, 2012	104	2012
The role of phospholipases A2 in schizophrenia MH Law, RGH Cotton, GE Berger Molecular psychiatry 11 (6), 547-556, 2006	91	2006
Vitamin D and overall cancer risk and cancer mortality: a Mendelian randomization study JS Ong, P Gharahkhani, J An, MH Law, DC Whiteman, RE Neale, ... Human molecular genetics 27 (24), 4315-4322, 2018	89	2018
Cell-type–specific eQTL of primary melanocytes facilitates identification of melanoma susceptibility genes T Zhang, J Choi, MA Kovacs, J Shi, M Xu, AM Goldstein, AJ Trower, ...	87	2018
Massively parallel reporter assays of melanoma risk variants identify MX2 as a gene promoting melanoma J Choi, T Zhang, A Vu, J Ablain, MM Makowski, LM Colli, M Xu, ... Nature communications 11 (1), 2718, 2020	85	2020

Sistem, işlemi şu anda gerçekleştiremiyor. Daha sonra yeniden deneyin.

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