Weihua Meng

2023

A Meta-Analysis of the Genome-Wide Association Studies on Two Genetically Correlated Phenotypes Suggests Four New Risk Loci for Headaches

23andMe Research Team, Feb 2023, In: Phenomics. 3, 1, p. 64-76 13 p.

Research output: Journal Publication › Article › peer-review

Open Access

3 Citations (Scopus)

Development and external validation of multivariable risk models to predict incident and resolved neuropathic pain: a DOLORisk Dundee study

Hébert, H. L., Veluchamy, A., Baskozos, G., Fardo, F., Van Ryckeghem, D., Pearson, E. R., Colvin, L. A., Crombez, G., Bennett, D. L. H., Meng, W., Palmer, C. N. A. & Smith, B. H., Feb 2023, In: Journal of Neurology. 270, 2, p. 1076-1094 19 p.

Research output: Journal Publication › Article › peer-review

Open Access

2 Citations (Scopus)

2022

Reciprocal interaction between depression and pain: Results from a comprehensive bidirectional Mendelian randomization study and functional annotation analysis

Tang, B., Meng, W., Hägg, S., Burgess, S. & Jiang, X., 1 Jan 2022, In: Pain. 163, 1, p. E40-E48

Research output: Journal Publication › Article › peer-review

Open Access

27 Citations (Scopus)

2021

Association of Genetic Variant at Chromosome 12q23.1 with Neuropathic Pain Susceptibility

Veluchamy, A., Hébert, H. L., Van Zuydam, N. R., Pearson, E. R., Campbell, A., Hayward, C., Meng, W., McCarthy, M. I., Bennett, D. L. H., Palmer, C. N. A. & Smith, B. H., 2 Dec 2021, In: JAMA network open. 4, 12, e2136560.

Research output: Journal Publication › Article › peer-review

Open Access

16 Citations (Scopus)

Changes in RT-PCR test results and symptoms during the menstrual cycle of female individuals infected with SARS-CoV-2: Report of two cases

Zheng, H., Tan, J., Ma, K. & Meng, W., Jan 2021, In: Journal of Medical Virology. 93, 1, p. 541-545 5 p.

Research output: Journal Publication › Article › peer-review

Open Access

5 Citations (Scopus)

Cohort profile: DOLORisk Dundee: A longitudinal study of chronic neuropathic pain

He´bert, H. L., Veluchamy, A., Baskozos, G., Fardo, F., Van Ryckeghem, D. M. L., Pascal, M. M. V., Jones, C., Milburn, K., Pearson, E. R., Crombez, G., Bennett, D. L. H., Meng, W., Palmer, C. N. A. & Smith, B. H., 5 May 2021, In: BMJ Open. 11, 5, e042887.

Research output: Journal Publication › Article › peer-review

Open Access

7 Citations (Scopus)

Sex-and age-specific genetic analysis of chronic back pain

Freidin, M. B., Tsepilov, Y. A., Stanaway, I. B., Meng, W., Hayward, C., Smith, B. H., Khoury, S., Parisien, M., Bortsov, A., Diatchenko, L., Børte, S., Winsvold, B. S., Brumpton, B. M., Zwart, J. A., Aulchenko, Y. S., Suri, P. & Williams, F. M. K., 1 Apr 2021, In: Pain. 162, 4, p. 1176-1187 12 p.

Research output: Journal Publication › Article › peer-review

Open Access

20 Citations (Scopus)

2020

A genome-wide association study finds genetic variants associated with neck or shoulder pain in UK Biobank

Meng, W., Chan, B. W., Harris, C., Freidin, M. B., Hebert, H. L., Adams, M. J., Campbell, A., Hayward, C., Zheng, H., Zhang, X., Colvin, L. A., Hales, T. G., Palmer, C. N. A., Williams, F. M. K., McIntosh, A. & Smith, B. H., 28 May 2020, In: Human Molecular Genetics. 29, 8, p. 1396-1404 9 p.

Research output: Journal Publication › Article › peer-review

Open Access

25 Citations (Scopus)

Genetic correlations between pain phenotypes and depression and neuroticism

Meng, W., Adams, M. J., Reel, P., Rajendrakumar, A., Huang, Y., Deary, I. J., Palmer, C. N. A., McIntosh, A. M. & Smith, B. H., 1 Mar 2020, In: European Journal of Human Genetics. 28, 3, p. 358-366 9 p.

Research output: Journal Publication › Article › peer-review

Open Access

46 Citations (Scopus)

Herpes zoster and postherpetic neuralgia in an elderly patient with critical COVID-19: A case report

Cao, X., Zhang, X., Meng, W. & Zheng, H., 2020, In: Journal of Pain Research. 13, p. 2361-2365 5 p.

Research output: Journal Publication › Article › peer-review

Open Access

15 Citations (Scopus)

2019

A genome-wide association study implicates that the TTC39C gene is associated with diabetic maculopathy with decreased visual acuity

Meng, W., Chan, B. W., Ezeonwumelu, C., Hébert, H. L., Campbell, A., Soler, V. & Palmer, C. N. A., 4 May 2019, In: Ophthalmic Genetics. 40, 3, p. 252-258 7 p.

Research output: Journal Publication › Article › peer-review

Open Access

8 Citations (Scopus)

Associations of autozygosity with a broad range of human phenotypes

Clark, D. W., Okada, Y., Moore, K. H. S., Mason, D., Pirastu, N., Gandin, I., Mattsson, H., Barnes, C. L. K., Lin, K., Zhao, J. H., Deelen, P., Rohde, R., Schurmann, C., Guo, X., Giulianini, F., Zhang, W., Medina-Gomez, C., Karlsson, R., Bao, Y. & Bartz, T. M. & 416 others, Baumbach, C., Biino, G., Bixley, M. J., Brumat, M., Chai, J. F., Corre, T., Cousminer, D. L., Dekker, A. M., Eccles, D. A., van Eijk, K. R., Fuchsberger, C., Gao, H., Germain, M., Gordon, S. D., de Haan, H. G., Harris, S. E., Hofer, E., Huerta-Chagoya, A., Igartua, C., Jansen, I. E., Jia, Y., Kacprowski, T., Karlsson, T., Kleber, M. E., Li, S. A., Li-Gao, R., Mahajan, A., Matsuda, K., Meidtner, K., Meng, W., Montasser, M. E., van der Most, P. J., Munz, M., Nutile, T., Palviainen, T., Prasad, G., Prasad, R. B., Priyanka, T. D. S., Rizzi, F., Salvi, E., Sapkota, B. R., Shriner, D., Skotte, L., Smart, M. C., Smith, A. V., van der Spek, A., Spracklen, C. N., Strawbridge, R. J., Tajuddin, S. M., Trompet, S., Turman, C., Verweij, N., Viberti, C., Wang, L., Warren, H. R., Wootton, R. E., Yanek, L. R., Yao, J., Yousri, N. A., Zhao, W., Adeyemo, A. A., Afaq, S., Aguilar-Salinas, C. A., Akiyama, M., Albert, M. L., Allison, M. A., Alver, M., Aung, T., Azizi, F., Bentley, A. R., Boeing, H., Boerwinkle, E., Borja, J. B., de Borst, G. J., Bottinger, E. P., Broer, L., Campbell, H., Chanock, S., Chee, M. L., Chen, G., Chen, Y. D. I., Chen, Z., Chiu, Y. F., Cocca, M., Collins, F. S., Concas, M. P., Corley, J., Cugliari, G., van Dam, R. M., Damulina, A., Daneshpour, M. S., Day, F. R., Delgado, G. E., Dhana, K., Doney, A. S. F., Dörr, M., Doumatey, A. P., Dzimiri, N., Ebenesersdóttir, S. S., Elliott, J., Elliott, P., Ewert, R., Felix, J. F., Fischer, K., Freedman, B. I., Girotto, G., Goel, A., Gögele, M., Goodarzi, M. O., Graff, M., Granot-Hershkovitz, E., Grodstein, F., Guarrera, S., Gudbjartsson, D. F., Guity, K., Gunnarsson, B., Guo, Y., Hagenaars, S. P., Haiman, C. A., Halevy, A., Harris, T. B., Hedayati, M., van Heel, D. A., Hirata, M., Höfer, I., Hsiung, C. A., Huang, J., Hung, Y. J., Ikram, M. A., Jagadeesan, A., Jousilahti, P., Kamatani, Y., Kanai, M., Kerrison, N. D., Kessler, T., Khaw, K. T., Khor, C. C., de Kleijn, D. P. V., Koh, W. P., Kolcic, I., Kraft, P., Krämer, B. K., Kutalik, Z., Kuusisto, J., Langenberg, C., Launer, L. J., Lawlor, D. A., Lee, I. T., Lee, W. J., Lerch, M. M., Li, L., Liu, J., Loh, M., London, S. J., Loomis, S., Lu, Y., Luan, J., Mägi, R., Manichaikul, A. W., Manunta, P., Másson, G., Matoba, N., Mei, X. W., Meisinger, C., Meitinger, T., Mezzavilla, M., Milani, L., Millwood, I. Y., Momozawa, Y., Moore, A., Morange, P. E., Moreno-Macías, H., Mori, T. A., Morrison, A. C., Muka, T., Murakami, Y., Murray, A. D., de Mutsert, R., Mychaleckyj, J. C., Nalls, M. A., Nauck, M., Neville, M. J., Nolte, I. M., Ong, K. K., Orozco, L., Padmanabhan, S., Pálsson, G., Pankow, J. S., Pattaro, C., Pattie, A., Polasek, O., Poulter, N., Pramstaller, P. P., Quintana-Murci, L., Räikkönen, K., Ralhan, S., Rao, D. C., van Rheenen, W., Rich, S. S., Ridker, P. M., Rietveld, C. A., Robino, A., van Rooij, F. J. A., Ruggiero, D., Saba, Y., Sabanayagam, C., Sabater-Lleal, M., Sala, C. F., Salomaa, V., Sandow, K., Schmidt, H., Scott, L. J., Scott, W. R., Sedaghati-Khayat, B., Sennblad, B., van Setten, J., Sever, P. J., Sheu, W. H. H., Shi, Y., Shrestha, S., Shukla, S. R., Sigurdsson, J. K., Sikka, T. T., Singh, J. R., Smith, B. H., Stančáková, A., Stanton, A., Starr, J. M., Stefansdottir, L., Straker, L., Sulem, P., Sveinbjornsson, G., Swertz, M. A., Taylor, A. M., Taylor, K. D., Terzikhan, N., Tham, Y. C., Thorleifsson, G., Thorsteinsdottir, U., Tillander, A., Tracy, R. P., Tusié-Luna, T., Tzoulaki, I., Vaccargiu, S., Vangipurapu, J., Veldink, J. H., Vitart, V., Völker, U., Vuoksimaa, E., Wakil, S. M., Waldenberger, M., Wander, G. S., Wang, Y. X., Wareham, N. J., Wild, S., Yajnik, C. S., Yuan, J. M., Zeng, L., Zhang, L., Zhou, J., Amin, N., Asselbergs, F. W., Bakker, S. J. L., Becker, D. M., Lehne, B., Bennett, D. A., van den Berg, L. H., Berndt, S. I., Bharadwaj, D., Bielak, L. F., Bochud, M., Boehnke, M., Bouchard, C., Bradfield, J. P., Brody, J. A., Campbell, A., Carmi, S., Caulfield, M. J., Cesarini, D., Chambers, J. C., Chandak, G. R., Cheng, C. Y., Ciullo, M., Cornelis, M., Cusi, D., Smith, G. D., Deary, I. J., Dorajoo, R., van Duijn, C. M., Ellinghaus, D., Erdmann, J., Eriksson, J. G., Evangelou, E., Evans, M. K., Faul, J. D., Feenstra, B., Feitosa, M., Foisy, S., Franke, A., Friedlander, Y., Gasparini, P., Gieger, C., Gonzalez, C., Goyette, P., Grant, S. F. A., Griffiths, L. R., Groop, L., Gudnason, V., Gyllensten, U., Hakonarson, H., Hamsten, A., van der Harst, P., Heng, C. K., Hicks, A. A., Hochner, H., Huikuri, H., Hunt, S. C., Jaddoe, V. W. V., De Jager, P. L., Johannesson, M., Johansson, Å., Jonas, J. B., Jukema, J. W., Junttila, J., Kaprio, J., Kardia, S. L. R., Karpe, F., Kumari, M., Laakso, M., van der Laan, S. W., Lahti, J., Laudes, M., Lea, R. A., Lieb, W., Lumley, T., Martin, N. G., März, W., Matullo, G., McCarthy, M. I., Medland, S. E., Merriman, T. R., Metspalu, A., Meyer, B. F., Mohlke, K. L., Montgomery, G. W., Mook-Kanamori, D., Munroe, P. B., North, K. E., Nyholt, D. R., O’connell, J. R., Ober, C., Oldehinkel, A. J., Palmas, W., Palmer, C., Pasterkamp, G. G., Patin, E., Pennell, C. E., Perusse, L., Peyser, P. A., Pirastu, M., Polderman, T. J. C., Porteous, D. J., Posthuma, D., Psaty, B. M., Rioux, J. D., Rivadeneira, F., Rotimi, C., Rotter, J. I., Rudan, I., Den Ruijter, H. M., Sanghera, D. K., Sattar, N., Schmidt, R., Schulze, M. B., Schunkert, H., Scott, R. A., Shuldiner, A. R., Sim, X., Small, N., Smith, J. A., Sotoodehnia, N., Tai, E. S., Teumer, A., Timpson, N. J., Toniolo, D., Tregouet, D. A., Tuomi, T., Vollenweider, P., Wang, C. A., Weir, D. R., Whitfield, J. B., Wijmenga, C., Wong, T. Y., Wright, J., Yang, J., Yu, L., Zemel, B. S., Zonderman, A. B., Perola, M., Magnusson, P. K. E., Uitterlinden, A. G., Kooner, J. S., Chasman, D. I., Loos, R. J. F., Franceschini, N., Franke, L., Haley, C. S., Hayward, C., Walters, R. G., Perry, J. R. B., Esko, T., Helgason, A., Stefansson, K., Joshi, P. K., Kubo, M. & Wilson, J. F., 1 Dec 2019, In: Nature Communications. 10, 1, 4957.

Research output: Journal Publication › Article › peer-review

Open Access

66 Citations (Scopus)

DOLORisk: Study protocol for a multi-centre observational study to understand the risk factors and determinants of neuropathic pain [version 2; referees: 2 approved]

Pascal, M. M. V., Themistocleous, A. C., Baron, R., Binder, A., Bouhassira, D., Crombez, G., Finnerup, N. B., Gierthmühlen, J., Granovsky, Y., Groop, L., Hebert, H. L., Jensen, T. S., Johnsen, K., McCarthy, M. I., Meng, W., Palmer, C. N. A., Rice, A. S. C., Serra, J., Solà, R. & Yarnitsky, D. & 3 others, Smith, B. H., Attal, N. & Bennett, D. L. H., 2019, In: Wellcome Open Research. 3, 63.

Research output: Journal Publication › Article › peer-review

Open Access

29 Citations (Scopus)

Genome-wide association study of knee pain identifies associations with GDF5 and COL27A1 in UK Biobank

The 23andMe Research Team, 1 Dec 2019, In: Communications Biology. 2, 1, 321.

Research output: Journal Publication › Article › peer-review

Open Access

42 Citations (Scopus)

Multiethnic genome-wide association study of diabetic retinopathy using liability threshold modeling of duration of diabetes and glycemic control

Family Investigation of Nephropathy and Diabetes-Eye Research Group & DCCT/EDIC Research Group, 1 Feb 2019, In: Diabetes. 68, 2, p. 441-456 16 p.

Research output: Journal Publication › Article › peer-review

Open Access

59 Citations (Scopus)

2018

A Genome-Wide Association Study Finds Genetic Associations with Broadly-Defined Headache in UK Biobank (N = 223,773)

Meng, W., Adams, M. J., Hebert, H. L., Deary, I. J., McIntosh, A. M. & Smith, B. H., Feb 2018, In: EBioMedicine. 28, p. 180-186 7 p.

Research output: Journal Publication › Article › peer-review

Open Access

55 Citations (Scopus)

A genome-wide association study suggests new evidence for an association of the NADPH Oxidase 4 (NOX4) gene with severe diabetic retinopathy in type 2 diabetes

Wellcome Trust Case Control Consortium 2 (WTCCC2), Surrogate markers for Micro- and Macro-vascular hard endpoints for Innovative diabetes Tools (SUMMIT) study group, Nov 2018, In: Acta Ophthalmologica. 96, 7, p. e811-e819

Research output: Journal Publication › Article › peer-review

Open Access

56 Citations (Scopus)

Cohort profile: Genetics of Diabetes Audit and Research in Tayside Scotland (GoDARTS)

Hébert, H. L., Shepherd, B., Milburn, K., Veluchamy, A., Meng, W., Carr, F., Donnelly, L. A., Tavendale, R., Leese, G., Colhoun, H. M., Dow, E., Morris, A. D., Doney, A. S., Lang, C. C., Pearson, E. R., Smith, B. H. & Palmer, C. N. A., Apr 2018, In: International Journal of Epidemiology. 47, 2, p. 380-381j

Research output: Journal Publication › Article › peer-review

Open Access

53 Citations (Scopus)

2017

A genome-wide association study suggests that MAPK14 is associated with diabetic foot ulcers

Meng, W., Veluchamy, A., Hébert, H. L., Campbell, A., Colhoun, H. M. & Palmer, C. N. A., 2017, In: British Journal of Dermatology. 177, 6, p. 1664-1670 7 p.

Research output: Journal Publication › Article › peer-review

Open Access

26 Citations (Scopus)

2016

A genome-wide association study provides new evidence that CACNA1C gene is associated with diabetic cataract

Chang, C., Zhang, K., Veluchamy, A., Hébert, H. L., Looker, H. C., Colhoun, H. M., Palmer, C. N. A. & Meng, W., Apr 2016, In: Investigative Ophthalmology and Visual Science. 57, 4, p. 2246-2250 5 p.

Research output: Journal Publication › Article › peer-review

Open Access

14 Citations (Scopus)

Genetic and Environmental Risk for Chronic Pain and the Contribution of Risk Variants for Major Depressive Disorder: A Family-Based Mixed-Model Analysis

McIntosh, A. M., Hall, L. S., Zeng, Y., Adams, M. J., Gibson, J., Wigmore, E., Hagenaars, S. P., Davies, G., Fernandez-Pujals, A. M., Campbell, A. I., Clarke, T. K., Hayward, C., Haley, C. S., Porteous, D. J., Deary, I. J., Smith, D. J., Nicholl, B. I., Hinds, D. A., Jones, A. V. & Scollen, S. & 3 others, Meng, W., Smith, B. H. & Hocking, L. J., Aug 2016, In: PLoS Medicine. 13, 8, e1002090.

Research output: Journal Publication › Article › peer-review

Open Access

47 Citations (Scopus)

Sequence and expression of complement factor H gene cluster variants and their roles in age-related macular degeneration risk

Hughes, A. E., Bridgett, S., Meng, W., Li, M., Curcio, C. A., Stambolian, D. & Bradley, D. T., May 2016, In: Investigative Ophthalmology and Visual Science. 57, 6, p. 2763-2769 7 p.

Research output: Journal Publication › Article › peer-review

Open Access

14 Citations (Scopus)

2015

A Genome-wide Association Study Provides Evidence of Sex-specific Involvement of Chr1p35.1 (ZSCAN20-TLR12P) and Chr8p23.1 (HMGB1P46) With Diabetic Neuropathic Pain

Meng, W., Deshmukh, H. A., Donnelly, L. A., Torrance, N., Colhoun, H. M., Palmer, C. N. A. & Smith, B. H., 1 Oct 2015, In: EBioMedicine. 2, 10, p. 1386-1393 8 p.

Research output: Journal Publication › Article › peer-review

Open Access

62 Citations (Scopus)

A genome-wide association study suggests an association of Chr8p21.3 (GFRA2) with diabetic neuropathic pain

Meng, W., Deshmukh, H. A., Van Zuydam, N. R., Liu, Y., Donnelly, L. A., Zhou, K., Morris, A. D., Colhoun, H. M., Palmer, C. N. A. & Smith, B. H., 1 Mar 2015, In: European Journal of Pain. 19, 3, p. 392-399 8 p.

Research output: Journal Publication › Article › peer-review

Open Access

67 Citations (Scopus)

Directional dominance on stature and cognition in diverse human populations

The Bio Bank Japan Project, 23 Jul 2015, In: Nature. 523, 7561, p. 459-462 4 p.

Research output: Journal Publication › Article › peer-review

Open Access

129 Citations (Scopus)

2013

Whole exome sequencing identifies a mutation for a novel form of corneal intraepithelial dyskeratosis

Soler, V. J., Tran-Viet, K. N., Galiacy, S. D., Limviphuvadh, V., Klemm, T. P., St Germain, E., Fournié, P. R., Guillaud, C., Maurer-Stroh, S., Hawthorne, F., Suarez, C., Kantelip, B., Afshari, N. A., Creveaux, I., Luo, X., Meng, W., Calvas, P., Cassagne, M., Arné, J. L. & Rozen, S. G. & 2 others, Malecaze, F. & Young, T. L., 2013, In: Journal of Medical Genetics. 50, 4, p. 246-254 9 p.

Research output: Journal Publication › Article › peer-review

Open Access

43 Citations (Scopus)

2012

A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French population

Meng, W., Butterworth, J., Bradley, D. T., Hughes, A. E., Soler, V., Calvas, P. & Malecaze, F., Dec 2012, In: Investigative Ophthalmology and Visual Science. 53, 13, p. 7983-7988 6 p.

Research output: Journal Publication › Article › peer-review

49 Citations (Scopus)

A novel GUCY2D mutation, V933A, causes central areolar choroidal dystrophy

Hughes, A. E., Meng, W., Lotery, A. J. & Bradley, D. T., Jul 2012, In: Investigative Ophthalmology and Visual Science. 53, 8, p. 4748-4753 6 p.

Research output: Journal Publication › Article › peer-review

16 Citations (Scopus)

Genetic factors for choroidal neovascularization associated with high myopia

Leveziel, N., Yu, Y., Reynolds, R., Tai, A., Meng, W., Caillaux, V., Calvas, P., Rosner, B., Malecaze, F., Souied, E. H. & Seddon, J. M., Jul 2012, In: Investigative Ophthalmology and Visual Science. 53, 8, p. 5004-5009 6 p.

Research output: Journal Publication › Article › peer-review

Open Access

46 Citations (Scopus)

Myopia and iris colour: A possible connection?

Meng, W., Butterworth, J., Calvas, P. & Malecaze, F., Jun 2012, In: Medical Hypotheses. 78, 6, p. 778-780 3 p.

Research output: Journal Publication › Article › peer-review

10 Citations (Scopus)

2011

Caractérisation du profil biométrique oculaire d'une population myope fort: la myopie forte correspond-elle un phénotype homogne ?

Translated title of the contribution: Characterization of the biometric eye profile of a high myopic population: Does high myopia correspond to a homogenous phenotype?Auriol, S., Butterworth, J., MacÉ, M., Meng, W. & Malecaze, F., Apr 2011, In: Journal Francais d'Ophtalmologie. 34, 4, p. 217-228 12 p.

Research output: Journal Publication › Article › peer-review

1 Citation (Scopus)

2010

Axial length: An underestimated endophenotype of myopia

Meng, W., Butterworth, J., Malecaze, F. & Calvas, P., Feb 2010, In: Medical Hypotheses. 74, 2, p. 252-253 2 p.

Research output: Journal Publication › Article › peer-review

16 Citations (Scopus)

2008

Chromosome 9p21.3 is associated with early-onset coronary heart disease in the Irish population

Meng, W., Hughes, A. E., Patterson, C. C., Belton, C., Kee, F. & McKeown, P. P., 2008, In: Disease Markers. 25, 2, p. 81-85 5 p.

Research output: Journal Publication › Article › peer-review

Open Access

20 Citations (Scopus)

Variants in the nestin gene and coronary heart disease

Meng, W., Patterson, C. C., Belton, C., Hughes, A. & McKeown, P. P., 2008, In: Circulation Journal. 72, 9, p. 1538-1539 2 p.

Research output: Journal Publication › Article › peer-review

Open Access

5 Citations (Scopus)

2007

Genetic variants of complement factor H gene are not associated with premature coronary heart disease: A family-based study in the Irish population

Meng, W., Hughes, A., Patterson, C. C., Belton, C., Kamaruddin, M. S., Horan, P. G., Kee, F. & McKeown, P. P., 18 Sept 2007, In: BMC Medical Genetics. 8, 62.

Research output: Journal Publication › Article › peer-review

Open Access

11 Citations (Scopus)

Dr Weihua Meng

Research output

Search results