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Search life-sciences literature (45,104,145 articles, preprints and more)

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A genome-wide association analysis reveals new pathogenic pathways in gout.
Major TJ, Takei R, Matsuo H, Leask MP, Sumpter NA, Topless RK, Shirai Y, Wang W, Cadzow MJ, Phipps-Green AJ, Li Z, Ji A, Merriman ME, Morice E, Kelley EE, Wei WH, McCormick SPA, Bixley MJ, Reynolds RJ, [...] Merriman TR
Nat Genet, 56(11):2392-2406, 15 Oct 2024
Cited by: 0 articles | PMID: 39406924
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Publisher Correction: A genome-wide association analysis reveals new pathogenic pathways in gout.
Major TJ, Takei R, Matsuo H, Leask MP, Sumpter NA, Topless RK, Shirai Y, Wang W, Cadzow MJ, Phipps-Green AJ, Li Z, Ji A, Merriman ME, Morice E, Kelley EE, Wei WH, McCormick SPA, Bixley MJ, Reynolds RJ, [...] Merriman TR
Nat Genet, 56(11):2577, 01 Nov 2024
Cited by: 0 articles | PMID: 39501129
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SMIM1 absence is associated with reduced energy expenditure and excess weight.
Stefanucci L, Moslemi C, Tomé AR, Virtue S, Bidault G, Gleadall NS, Watson LPE, Kwa JE, Burden F, Farrow S, DBDS Genetic Consortium, Chen J, MAGIC, Võsa U, Burling K, Walker L, Ord J, Barker P, Warner J, [...] Frontini M
Med, 5(9):1083-1095.e6, 20 Jun 2024
Cited by: 0 articles | PMID: 38906141
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Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH.
Li JH, Brenner LN, Kaur V, Figueroa K, Schroeder P, Huerta-Chagoya A, MAGIC Investigators, Diabetes Prevention Program (DPP) Research Group, Udler MS, Leong A, Mercader JM, Florez JC
Diabetologia, 66(7):1260-1272, 26 May 2023
Cited by: 2 articles | PMID: 37233759 | PMCID: PMC10790310
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A genome-wide association analysis of 2,622,830 individuals reveals new pathogenic pathways in gout
Major TJ, Takei R, Matsuo H, Leask MP, Topless RK, Shirai Y, Li Z, Ji A, Cadzow MJ, Sumpter NA, Merriman ME, Phipps-Green AJ, Urquiaga M, Kelley EE, King RD, Lewis SE, Maxwell BA, Wei W, McCormick SP, [...] Merriman TR
medRxiv, 29 Nov 2022
Cited by: 0 articles | PPR: PPR577345
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Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.
Winkler TW, Rasheed H, Teumer A, Gorski M, Rowan BX, Stanzick KJ, Thomas LF, Tin A, Hoppmann A, Chu AY, Tayo B, Thio CHL, Cusi D, Chai JF, Sieber KB, Horn K, Li M, Scholz M, Cocca M, [...] Heid IM
Commun Biol, 5(1):580, 13 Jun 2022
Cited by: 14 articles | PMID: 35697829 | PMCID: PMC9192715
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Variants associated with HHIP expression have sex-differential effects on lung function
Fawcett KA, Obeidat M, Melbourne CA, Shrine N, Guyatt AL, John C, Luan J, Richmond A, Moksnes MR, Granell R, Weiss S, Imboden M, May-Wilson S, Hysi P, Boutin TS, Portas L, Flexeder C, Harris SE, Wang CA, [...] Wain LV
Wellcome Open Res, 24 May 2021
Cited by: 0 articles | PPR: PPR344811
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The trans-ancestral genomic architecture of glycemic traits.
Chen J, Spracklen CN, Marenne G, Varshney A, Corbin LJ, Luan J, Willems SM, Wu Y, Zhang X, Horikoshi M, Boutin TS, Mägi R, Waage J, Li-Gao R, Chan KHK, Yao J, Anasanti MD, Chu AY, Claringbould A, [...] Meta-Analysis of Glucose and Insulin-related Traits Consortium (MAGIC)
Nat Genet, 53(6):840-860, 31 May 2021
Cited by: 302 articles | PMID: 34059833 | PMCID: PMC7610958
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Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Folkersen L, Gustafsson S, Wang Q, Hansen DH, Hedman ÅK, Schork A, Page K, Zhernakova DV, Wu Y, Peters J, Eriksson N, Bergen SE, Boutin TS, Bretherick AD, Enroth S, Kalnapenkis A, Gådin JR, Suur BE, Chen Y, [...] Mälarstig A
Nat Metab, 2(10):1135-1148, 16 Oct 2020
Cited by: 281 articles | PMID: 33067605 | PMCID: PMC7611474
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The Trans-Ancestral Genomic Architecture of Glycaemic Traits
Chen J, Spracklen CN, Marenne G, Varshney A, Corbin LJ, Luan J, Willems S, Wu Y, Zhang X, Horikoshi M, Boutin TS, Mägi R, Waage J, Pitsilides A, Li-Gao R, Hang K, Yao J, Anasanti MD, Chu AY, [...] M D
bioRxiv, 25 Jul 2020
Cited by: 0 articles | PPR: PPR192295
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Linking protein to phenotype with Mendelian Randomization detects 38 proteins with causal roles in human diseases and traits.
Bretherick AD, Canela-Xandri O, Joshi PK, Clark DW, Rawlik K, Boutin TS, Zeng Y, Amador C, Navarro P, Rudan I, Wright AF, Campbell H, Vitart V, Hayward C, Wilson JF, Tenesa A, Ponting CP, Baillie JK, Haley C
PLoS Genet, 16(7):e1008785, 06 Jul 2020
Cited by: 22 articles | PMID: 32628676 | PMCID: PMC7337286
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Insights into the genetic basis of retinal detachment.
Boutin TS, Charteris DG, Chandra A, Campbell S, Hayward C, Campbell A, UK Biobank Eye & Vision Consortium, Nandakumar P, Hinds D, 23andMe Research Team, Mitry D, Vitart V
Hum Mol Genet, 29(4):689-702, 01 Mar 2020
Cited by: 22 articles | PMID: 31816047 | PMCID: PMC7068119
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Characterisation of an inflammation-related epigenetic score and its association with cognitive ability.
Stevenson AJ, McCartney DL, Hillary RF, Campbell A, Morris SW, Bermingham ML, Walker RM, Evans KL, Boutin TS, Hayward C, McRae AF, McColl BW, Spires-Jones TL, McIntosh AM, Deary IJ, Marioni RE
Clin Epigenetics, 12(1):113, 27 Jul 2020
Cited by: 26 articles | PMID: 32718350 | PMCID: PMC7385981
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Variants associated with HHIP expression have sex-differential effects on lung function.
Fawcett KA, Obeidat M, Melbourne C, Shrine N, Guyatt AL, John C, Luan J, Richmond A, Moksnes MR, Granell R, Weiss S, Imboden M, May-Wilson S, Hysi P, Boutin TS, Portas L, Flexeder C, Harris SE, Wang CA, [...] Wain LV
Wellcome Open Res, 5:111, 01 Jan 2020
Cited by: 3 articles | PMID: 33728380 | PMCID: PMC7938335
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Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels.
Tin A, Marten J, Halperin Kuhns VL, Li Y, Wuttke M, Kirsten H, Sieber KB, Qiu C, Gorski M, Yu Z, Giri A, Sveinbjornsson G, Li M, Chu AY, Hoppmann A, O'Connor LJ, Prins B, Nutile T, Noce D, [...] Köttgen A
Nat Genet, 51(10):1459-1474, 02 Oct 2019
Cited by: 181 articles | PMID: 31578528 | PMCID: PMC6858555
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Multi-trait genome-wide association study identifies new loci associated with optic disc parameters.
Bonnemaijer PWM, Leeuwen EMV, Iglesias AI, Gharahkhani P, Vitart V, Khawaja AP, Simcoe M, Höhn R, Cree AJ, Igo RP, International Glaucoma Genetics Consortium, NEIGHBORHOOD consortium, UK Biobank Eye and Vision Consortium, Gerhold-Ay A, Nickels S, Wilson JF, Hayward C, Boutin TS, Polašek O, [...] Duijn CMV
Commun Biol, 2:435, 27 Nov 2019
Cited by: 22 articles | PMID: 31798171 | PMCID: PMC6881308
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Characterisation of an inflammation-related epigenetic score and its association with cognitive ability
Stevenson AJ, McCartney DL, Hillary RF, Campbell A, Morris SW, Bermingham ML, Walker RM, Evans KL, Boutin TS, Hayward C, McRae AF, McColl BW, Spires-Jones TL, McIntosh AM, Deary IJ, Marioni RE
bioRxiv, 13 Oct 2019
Cited by: 0 articles | PPR: PPR97807
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An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort.
Kerr SM, Klaric L, Halachev M, Hayward C, Boutin TS, Meynert AM, Semple CA, Tuiskula AM, Swan H, Santoyo-Lopez J, Vitart V, Haley C, Dean J, Miedzybrodzka Z, Aitman TJ, Wilson JF
Sci Rep, 9(1):10964, 29 Jul 2019
Cited by: 11 articles | PMID: 31358886 | PMCID: PMC6662790
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Publisher Correction: Parent of origin genetic effects on methylation in humans are common and influence complex trait variation.
Zeng Y, Amador C, Xia C, Marioni R, Sproul D, Walker RM, Morris SW, Bretherick A, Canela-Xandri O, Boutin TS, Clark DW, Campbell A, Rawlik K, Hayward C, Nagy R, Tenesa A, Porteous DJ, Wilson JF, Deary IJ, [...] Haley CS
Nat Commun, 10(1):2069, 01 May 2019
Cited by: 0 articles | PMID: 31043600 | PMCID: PMC6494888
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Proteome-by-phenome Mendelian Randomisation detects 38 proteins with causal roles in human diseases and traits
Bretherick AD, Canela-Xandri O, Joshi PK, Clark DW, Rawlik K, Boutin TS, Zeng Y, Amador C, Navarro P, Rudan I, Wright AF, Campbell H, Vitart V, Hayward C, Wilson JF, Tenesa A, Ponting CP, Kenneth Baillie J, Haley C
bioRxiv, 10 May 2019
Cited by: 0 articles | PPR: PPR78757
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Parent of origin genetic effects on methylation in humans are common and influence complex trait variation.
Zeng Y, Amador C, Xia C, Marioni R, Sproul D, Walker RM, Morris SW, Bretherick A, Canela-Xandri O, Boutin TS, Clark DW, Campbell A, Rawlik K, Hayward C, Nagy R, Tenesa A, Porteous DJ, Wilson JF, Deary IJ, [...] Haley CS
Nat Commun, 10(1):1383, 27 Mar 2019
Cited by: 24 articles | PMID: 30918249 | PMCID: PMC6437195
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Insight into the genetic aetiology of retinal detachment by combining small clinical and large population-based datasets
Boutin TS, Charteris DG, Chandra A, Campbell S, Hayward C, Campbell A, UK Biobank Eye & Vision Consortium, Nandakumar P, Hinds D, 23andMe Research Team, Mitry D, Vitart V
bioRxiv, 18 Mar 2019
Cited by: 0 articles | PPR: PPR73547
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Trans-ethnic association study of blood pressure determinants in over 750,000 individuals.
Giri A, Hellwege JN, Keaton JM, Park J, Qiu C, Warren HR, Torstenson ES, Kovesdy CP, Sun YV, Wilson OD, Robinson-Cohen C, Roumie CL, Chung CP, Birdwell KA, Damrauer SM, DuVall SL, Klarin D, Cho K, Wang Y, [...] Edwards TL
Nat Genet, 51(1):51-62, 21 Dec 2018
Cited by: 227 articles | PMID: 30578418 | PMCID: PMC6365102
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A catalog of genetic loci associated with kidney function from analyses of a million individuals.
Wuttke M, Li Y, Li M, Sieber KB, Feitosa MF, Gorski M, Tin A, Wang L, Chu AY, Hoppmann A, Kirsten H, Giri A, Chai JF, Sveinbjornsson G, Tayo BO, Nutile T, Fuchsberger C, Marten J, Cocca M, [...] Pattaro C
Nat Genet, 51(6):957-972, 31 May 2019
Cited by: 406 articles | PMID: 31152163 | PMCID: PMC6698888
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SNPs associated withHHIPexpression have differential effects on lung function in males and females
Fawcett K, Obeidat M, Melbourne C, Shrine N, Guyatt A, John C, Luan J, Richmond A, Moksnes M, Granell R, Weiss S, Imboden M, May-Wilson S, Hysi P, Boutin T, Portas L, Flexeder C, Harris S, Wang C, [...] Wain L
bioRxiv, 31 Mar 2019
Cited by: 0 articles | PPR: PPR74925
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1-25 of 33 results

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Search life-sciences literature (45,104,145 articles, preprints and more)

Search results

A genome-wide association analysis reveals new pathogenic pathways in gout.

Publisher Correction: A genome-wide association analysis reveals new pathogenic pathways in gout.

SMIM1 absence is associated with reduced energy expenditure and excess weight.

Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH.

A genome-wide association analysis of 2,622,830 individuals reveals new pathogenic pathways in gout

Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.

Variants associated with HHIP expression have sex-differential effects on lung function

The trans-ancestral genomic architecture of glycemic traits.

Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.

The Trans-Ancestral Genomic Architecture of Glycaemic Traits

Linking protein to phenotype with Mendelian Randomization detects 38 proteins with causal roles in human diseases and traits.

Insights into the genetic basis of retinal detachment.

Characterisation of an inflammation-related epigenetic score and its association with cognitive ability.

Variants associated with HHIP expression have sex-differential effects on lung function.

Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels.

Multi-trait genome-wide association study identifies new loci associated with optic disc parameters.

Characterisation of an inflammation-related epigenetic score and its association with cognitive ability

An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort.

Publisher Correction: Parent of origin genetic effects on methylation in humans are common and influence complex trait variation.

Proteome-by-phenome Mendelian Randomisation detects 38 proteins with causal roles in human diseases and traits

Parent of origin genetic effects on methylation in humans are common and influence complex trait variation.

Insight into the genetic aetiology of retinal detachment by combining small clinical and large population-based datasets

Trans-ethnic association study of blood pressure determinants in over 750,000 individuals.

A catalog of genetic loci associated with kidney function from analyses of a million individuals.

SNPs associated withHHIPexpression have differential effects on lung function in males and females

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