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Items: 1 to 50 of 729

1.

Letter to the Editor - BTS/SIGN Guideline Query Doubling the dose of inhaled steroids.

Barnes N, Higgins B, Douglas G.

Prim Care Respir J. 2003 Sep;12(3):99. doi: 10.1038/pcrj.2003.57. Epub 2003 Sep 1. No abstract available.

2.

In vivo genotoxicity testing strategies: Report from the 7th International workshop on genotoxicity testing (IWGT).

Kirkland D, Uno Y, Luijten M, Beevers C, van Benthem J, Burlinson B, Dertinger S, Douglas GR, Hamada S, Horibata K, Lovell DP, Manjanatha M, Martus HJ, Mei N, Morita T, Ohyama W, Williams A.

Mutat Res. 2019 Nov;847:403035. doi: 10.1016/j.mrgentox.2019.03.008. Epub 2019 Apr 25.

PMID:
31699340
3.

Specific Immunologic Countermeasure Protocol for Deep-Space Exploration Missions.

Makedonas G, Mehta S, Choukèr A, Simpson RJ, Marshall G, Orange JS, Aunon-Chancellor S, Smith SM, Zwart SR, Stowe RP, Heer M, Ponomarev S, Whitmire A, Frippiat JP, Douglas GL, Krieger SS, Lorenzi H, Buchheim JI, Ginsburg GS, Ott CM, Downs M, Pierson D, Baecker N, Sams C, Crucian B.

Front Immunol. 2019 Oct 11;10:2407. doi: 10.3389/fimmu.2019.02407. eCollection 2019. No abstract available.

4.

'He was distraught, I was distraught.' Parents' experiences of accessing emergency care following an avulsion injury to their child.

Kenny K, Vinall-Collier K, Douglas G, Day PF.

Br Dent J. 2019 Oct;227(8):705-710. doi: 10.1038/s41415-019-0738-0.

PMID:
31654007
5.

Missense variants in TAF1 and developmental phenotypes: challenges of determining pathogenicity.

Cheng H, Capponi S, Wakeling E, Marchi E, Li Q, Zhao M, Weng C, Stefan PG, Ahlfors H, Kleyner R, Rope A, Lumaka A, Lukusa P, Devriendt K, Vermeesch J, Posey JE, Palmer EE, Murray L, Leon E, Diaz J, Worgan L, Mallawaarachchi A, Vogt J, de Munnik SA, Dreyer L, Baynam G, Ewans L, Stark Z, Lunke S, Gonçalves AR, Soares G, Oliveira J, Fassi E, Willing M, Waugh JL, Faivre L, Riviere JB, Moutton S, Mohammed S, Payne K, Walsh L, Begtrup A, Guillen Sacoto MJ, Douglas G, Alexander N, Buckley MF, Mark PR, Adès LC, Sandaradura SA, Lupski JR, Roscioli T, Agrawal PB, Kline AD; Deciphering Developmental Disorders Study, Wang K, Timmers HTM, Lyon GJ.

Hum Mutat. 2019 Oct 23. doi: 10.1002/humu.23936. [Epub ahead of print]

PMID:
31646703
6.

Mutation as a Toxicological Endpoint for Regulatory Decision-Making.

Heflich RH, Johnson GE, Zeller A, Marchetti F, Douglas GR, Witt KL, Gollapudi BB, White PA.

Environ Mol Mutagen. 2019 Oct 10. doi: 10.1002/em.22338. [Epub ahead of print]

PMID:
31600846
7.

Remuneration of primary dental care in England: a qualitative framework analysis of perspectives of a new service delivery model incorporating incentives for improved access, quality and health outcomes.

Robinson PG, Douglas GVA, Gibson BJ, Godson J, Vinall-Collier K, Pavitt S, Hulme C.

BMJ Open. 2019 Oct 3;9(10):e031886. doi: 10.1136/bmjopen-2019-031886.

8.

The views and experiences of general dental practitioners (GDP's) in West Yorkshire who used the International Caries Detection and Assessment System (ICDAS) in research.

Khattak MI, Csikar J, Vinall K, Douglas G.

PLoS One. 2019 Oct 4;14(10):e0223376. doi: 10.1371/journal.pone.0223376. eCollection 2019.

9.

A key role for the novel coronary artery disease gene JCAD in atherosclerosis via shear stress mechanotransduction.

Douglas G, Mehta V, Zen AAH, Akoumianakis I, Goel A, Rashbrook VS, Trelfa L, Donovan L, Drydale E, Chuaiphichai S, Antoniades C, Watkins H, Kyriakou T, Tzima E, Channon KM.

Cardiovasc Res. 2019 Oct 4. pii: cvz263. doi: 10.1093/cvr/cvz263. [Epub ahead of print]

PMID:
31584065
10.

Adipose tissue-derived WNT5A regulates vascular redox signaling in obesity via USP17/RAC1-mediated activation of NADPH oxidases.

Akoumianakis I, Sanna F, Margaritis M, Badi I, Akawi N, Herdman L, Coutinho P, Fagan H, Antonopoulos AS, Oikonomou EK, Thomas S, Chiu AP, Chuaiphichai S, Kotanidis CP, Christodoulides C, Petrou M, Krasopoulos G, Sayeed R, Lv L, Hale A, Naeimi Kararoudi M, McNeill E, Douglas G, George S, Tousoulis D, Channon KM, Antoniades C.

Sci Transl Med. 2019 Sep 18;11(510). pii: eaav5055. doi: 10.1126/scitranslmed.aav5055.

PMID:
31534019
11.

CariesCare practice guide: consensus on evidence into practice.

Martignon S, Pitts NB, Goffin G, Mazevet M, Douglas GVA, Newton JT, Twetman S, Deery C, Doméjean S, Jablonski-Momeni A, Banerjee A, Kolker J, Ricketts D, Santamaria RM.

Br Dent J. 2019 Sep;227(5):353-362. doi: 10.1038/s41415-019-0678-8.

PMID:
31520031
12.

Current and Promising Approaches to Identify Horizontal Gene Transfer Events in Metagenomes.

Douglas GM, Langille MGI.

Genome Biol Evol. 2019 Oct 1;11(10):2750-2766. doi: 10.1093/gbe/evz184.

13.

A Return to the Origin of the EMGS: Rejuvenating the Quest for Human Germ Cell Mutagens and Determining the Risk to Future Generations.

Marchetti F, Douglas GR, Yauk CL.

Environ Mol Mutagen. 2019 Aug 31. doi: 10.1002/em.22327. [Epub ahead of print]

PMID:
31472026
14.

Metagenomic Functional Shifts to Plant Induced Environmental Changes.

Yurgel SN, Nearing JT, Douglas GM, Langille MGI.

Front Microbiol. 2019 Jul 26;10:1682. doi: 10.3389/fmicb.2019.01682. eCollection 2019.

15.

Author Correction: Reproducible, interactive, scalable and extensible microbiome data science using QIIME 2.

Bolyen E, Rideout JR, Dillon MR, Bokulich NA, Abnet CC, Al-Ghalith GA, Alexander H, Alm EJ, Arumugam M, Asnicar F, Bai Y, Bisanz JE, Bittinger K, Brejnrod A, Brislawn CJ, Brown CT, Callahan BJ, Caraballo-Rodríguez AM, Chase J, Cope EK, Da Silva R, Diener C, Dorrestein PC, Douglas GM, Durall DM, Duvallet C, Edwardson CF, Ernst M, Estaki M, Fouquier J, Gauglitz JM, Gibbons SM, Gibson DL, Gonzalez A, Gorlick K, Guo J, Hillmann B, Holmes S, Holste H, Huttenhower C, Huttley GA, Janssen S, Jarmusch AK, Jiang L, Kaehler BD, Kang KB, Keefe CR, Keim P, Kelley ST, Knights D, Koester I, Kosciolek T, Kreps J, Langille MGI, Lee J, Ley R, Liu YX, Loftfield E, Lozupone C, Maher M, Marotz C, Martin BD, McDonald D, McIver LJ, Melnik AV, Metcalf JL, Morgan SC, Morton JT, Naimey AT, Navas-Molina JA, Nothias LF, Orchanian SB, Pearson T, Peoples SL, Petras D, Preuss ML, Pruesse E, Rasmussen LB, Rivers A, Robeson MS 2nd, Rosenthal P, Segata N, Shaffer M, Shiffer A, Sinha R, Song SJ, Spear JR, Swafford AD, Thompson LR, Torres PJ, Trinh P, Tripathi A, Turnbaugh PJ, Ul-Hasan S, van der Hooft JJJ, Vargas F, Vázquez-Baeza Y, Vogtmann E, von Hippel M, Walters W, Wan Y, Wang M, Warren J, Weber KC, Williamson CHD, Willis AD, Xu ZZ, Zaneveld JR, Zhang Y, Zhu Q, Knight R, Caporaso JG.

Nat Biotechnol. 2019 Sep;37(9):1091. doi: 10.1038/s41587-019-0252-6.

PMID:
31399723
16.

Reproducible, interactive, scalable and extensible microbiome data science using QIIME 2.

Bolyen E, Rideout JR, Dillon MR, Bokulich NA, Abnet CC, Al-Ghalith GA, Alexander H, Alm EJ, Arumugam M, Asnicar F, Bai Y, Bisanz JE, Bittinger K, Brejnrod A, Brislawn CJ, Brown CT, Callahan BJ, Caraballo-Rodríguez AM, Chase J, Cope EK, Da Silva R, Diener C, Dorrestein PC, Douglas GM, Durall DM, Duvallet C, Edwardson CF, Ernst M, Estaki M, Fouquier J, Gauglitz JM, Gibbons SM, Gibson DL, Gonzalez A, Gorlick K, Guo J, Hillmann B, Holmes S, Holste H, Huttenhower C, Huttley GA, Janssen S, Jarmusch AK, Jiang L, Kaehler BD, Kang KB, Keefe CR, Keim P, Kelley ST, Knights D, Koester I, Kosciolek T, Kreps J, Langille MGI, Lee J, Ley R, Liu YX, Loftfield E, Lozupone C, Maher M, Marotz C, Martin BD, McDonald D, McIver LJ, Melnik AV, Metcalf JL, Morgan SC, Morton JT, Naimey AT, Navas-Molina JA, Nothias LF, Orchanian SB, Pearson T, Peoples SL, Petras D, Preuss ML, Pruesse E, Rasmussen LB, Rivers A, Robeson MS 2nd, Rosenthal P, Segata N, Shaffer M, Shiffer A, Sinha R, Song SJ, Spear JR, Swafford AD, Thompson LR, Torres PJ, Trinh P, Tripathi A, Turnbaugh PJ, Ul-Hasan S, van der Hooft JJJ, Vargas F, Vázquez-Baeza Y, Vogtmann E, von Hippel M, Walters W, Wan Y, Wang M, Warren J, Weber KC, Williamson CHD, Willis AD, Xu ZZ, Zaneveld JR, Zhang Y, Zhu Q, Knight R, Caporaso JG.

Nat Biotechnol. 2019 Aug;37(8):852-857. doi: 10.1038/s41587-019-0209-9. No abstract available. Erratum in: Nat Biotechnol. 2019 Sep;37(9):1091.

PMID:
31341288
17.

Nox2 contributes to age-related oxidative damage to neurons and the cerebral vasculature.

Fan LM, Geng L, Cahill-Smith S, Liu F, Douglas G, Mckenzie CA, Smith C, Brooks G, Channon KM, Li JM.

J Clin Invest. 2019 Jul 22;129(8):3374-3386. doi: 10.1172/JCI125173. eCollection 2019 Jul 22.

18.

Corrigendum to "Identifying germ cell mutagens using OECD test guideline 488 (transgenic rodent somatic and germ cell Gene mutation assays) and integration with somatic cell testing." [Mutat. Res. 832-833 (2018) 7-18].

Marchetti F, Aardema MJ, Beevers C, van Benthem J, Godschalk R, Williams A, Yauk CL, Young R, Douglas GR.

Mutat Res. 2019 Aug;844:70-71. doi: 10.1016/j.mrgentox.2019.05.018. Epub 2019 Jun 7. No abstract available.

19.

Corrigendum to "Simulation of mouse and rat spermatogenesis to inform genotoxicity testing using OECD test guideline 488" [Mutat. Res. 832-833 (2018) 19-28].

Marchetti F, Aardema MJ, Beevers C, van Benthem J, Douglas GR, Godschalk R, Yauk CL, Young R, Williams A.

Mutat Res. 2019 Aug;844:69. doi: 10.1016/j.mrgentox.2019.05.019. Epub 2019 Jun 12. No abstract available.

20.

Confirmation that variants in TTI2 are responsible for autosomal recessive intellectual disability.

Ziegler A, Bader P, McWalter K, Douglas G, Houdayer C, Bris C, Rouleau S, Coutant R, Colin E, Bonneau D.

Clin Genet. 2019 Oct;96(4):354-358. doi: 10.1111/cge.13603. Epub 2019 Jul 17.

PMID:
31290144
21.

Identifying the barriers and facilitators for homeless people to achieve good oral health.

Csikar J, Vinall-Collier K, Richemond JM, Talbot J, Serban ST, Douglas GVA.

Community Dent Health. 2019 May 30;36(2):137-142. doi: 10.1922/CDH_4488Csikar06.

PMID:
31070874
22.

Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.

Snijders Blok L, Rousseau J, Twist J, Ehresmann S, Takaku M, Venselaar H, Rodan LH, Nowak CB, Douglas J, Swoboda KJ, Steeves MA, Sahai I, Stumpel CTRM, Stegmann APA, Wheeler P, Willing M, Fiala E, Kochhar A, Gibson WT, Cohen ASA, Agbahovbe R, Innes AM, Au PYB, Rankin J, Anderson IJ, Skinner SA, Louie RJ, Warren HE, Afenjar A, Keren B, Nava C, Buratti J, Isapof A, Rodriguez D, Lewandowski R, Propst J, van Essen T, Choi M, Lee S, Chae JH, Price S, Schnur RE, Douglas G, Wentzensen IM, Zweier C, Reis A, Bialer MG, Moore C, Koopmans M, Brilstra EH, Monroe GR, van Gassen KLI, van Binsbergen E, Newbury-Ecob R, Bownass L, Bader I, Mayr JA, Wortmann SB, Jakielski KJ, Strand EA, Kloth K, Bierhals T; DDD study, Roberts JD, Petrovich RM, Machida S, Kurumizaka H, Lelieveld S, Pfundt R, Jansen S, Deriziotis P, Faivre L, Thevenon J, Assoum M, Shriberg L, Kleefstra T, Brunner HG, Wade PA, Fisher SE, Campeau PM.

Nat Commun. 2019 May 2;10(1):2079. doi: 10.1038/s41467-019-10161-9.

23.

SON haploinsufficiency causes impaired pre-mRNA splicing of CAKUT genes and heterogeneous renal phenotypes.

Kim JH, Park EY, Chitayat D, Stachura DL, Schaper J, Lindstrom K, Jewett T, Wieczorek D, Draaisma JM, Sinnema M, Hoeberigs C, Hempel M, Bachman KK, Seeley AH, Stone JK, Kong HK, Vukadin L, Richard A, Shinde DN, McWalter K, Si YC, Douglas G, Lim ST, Vissers LELM, Lemaire M, Ahn EE.

Kidney Int. 2019 Jun;95(6):1494-1504. doi: 10.1016/j.kint.2019.01.025. Epub 2019 Mar 15.

PMID:
31005274
24.

Factors associated with antibiotic prescribing for adults with acute conditions: an umbrella review across primary care and a systematic review focusing on primary dental care.

Thompson W, Tonkin-Crine S, Pavitt SH, McEachan RRC, Douglas GVA, Aggarwal VR, Sandoe JAT.

J Antimicrob Chemother. 2019 Aug 1;74(8):2139-2152. doi: 10.1093/jac/dkz152.

25.

Barriers and facilitators for prevention in Danish dental care.

Rosing K, Leggett H, Csikar J, Vinall-Collier K, Christensen LB, Whelton H, Douglas GVA.

Acta Odontol Scand. 2019 Aug;77(6):439-451. doi: 10.1080/00016357.2019.1587503. Epub 2019 Mar 25.

26.

Engineering and kinetic aspects of bacterial uranium reduction for the remediation of uranium contaminated environments.

Lakaniemi AM, Douglas GB, Kaksonen AH.

J Hazard Mater. 2019 Jun 5;371:198-212. doi: 10.1016/j.jhazmat.2019.02.074. Epub 2019 Feb 21. Review.

PMID:
30851673
27.

De novo variants in HK1 associated with neurodevelopmental abnormalities and visual impairment.

Okur V, Cho MT, van Wijk R, van Oirschot B, Picker J, Coury SA, Grange D, Manwaring L, Krantz I, Muraresku CC, Hulick PJ, May H, Pierce E, Place E, Bujakowska K, Telegrafi A, Douglas G, Monaghan KG, Begtrup A, Wilson A, Retterer K, Anyane-Yeboa K, Chung WK.

Eur J Hum Genet. 2019 Jul;27(7):1081-1089. doi: 10.1038/s41431-019-0366-9. Epub 2019 Feb 18.

PMID:
30778173
28.

Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.

Blok LS, Rousseau J, Twist J, Ehresmann S, Takaku M, Venselaar H, Rodan LH, Nowak CB, Douglas J, Swoboda KJ, Steeves MA, Sahai I, Stumpel CTRM, Stegmann APA, Wheeler P, Willing M, Fiala E, Kochhar A, Gibson WT, Cohen ASA, Agbahovbe R, Innes AM, Au PYB, Rankin J, Anderson IJ, Skinner SA, Louie RJ, Warren HE, Afenjar A, Keren B, Nava C, Buratti J, Isapof A, Rodriguez D, Lewandowski R, Propst J, van Essen T, Choi M, Lee S, Chae JH, Price S, Schnur RE, Douglas G, Wentzensen IM, Zweier C, Reis A, Bialer MG, Moore C, Koopmans M, Brilstra EH, Monroe GR, van Gassen KLI, van Binsbergen E, Newbury-Ecob R, Bownass L, Bader I, Mayr JA, Wortmann SB, Jakielski KJ, Strand EA, Kloth K, Bierhals T; DDD study, Roberts JD, Petrovich RM, Machida S, Kurumizaka H, Lelieveld S, Pfundt R, Jansen S, Deriziotis P, Faivre L, Thevenon J, Assoum M, Shriberg L, Kleefstra T, Brunner HG, Wade PA, Fisher SE, Campeau PM.

Nat Commun. 2019 Feb 15;10(1):883. doi: 10.1038/s41467-019-08800-2.

29.

A comparison of transgenic rodent mutation and in vivo comet assay responses for 91 chemicals.

Kirkland D, Levy DD, LeBaron MJ, Aardema MJ, Beevers C, Bhalli J, Douglas GR, Escobar PA, Farabaugh CS, Guerard M, Johnson GE, Kulkarni R, Le Curieux F, Long AS, Lott J, Lovell DP, Luijten M, Marchetti F, Nicolette JJ, Pfuhler S, Roberts DJ, Stankowski LF Jr, Thybaud V, Weiner SK, Williams A, Witt KL, Young R.

Mutat Res Genet Toxicol Environ Mutagen. 2019 Mar;839:21-35. doi: 10.1016/j.mrgentox.2019.01.007. Epub 2019 Jan 18.

30.

Variants in TCF20 in neurodevelopmental disability: description of 27 new patients and review of literature.

Torti E, Keren B, Palmer EE, Zhu Z, Afenjar A, Anderson IJ, Andrews MV, Atkinson C, Au M, Berry SA, Bowling KM, Boyle J, Buratti J, Cathey SS, Charles P, Cogne B, Courtin T, Escobar LF, Finley SL, Graham JM Jr, Grange DK, Heron D, Hewson S, Hiatt SM, Hibbs KA, Jayakar P, Kalsner L, Larcher L, Lesca G, Mark PR, Miller K, Nava C, Nizon M, Pai GS, Pappas J, Parsons G, Payne K, Putoux A, Rabin R, Sabatier I, Shinawi M, Shur N, Skinner SA, Valence S, Warren H, Whalen S, Crunk A, Douglas G, Monaghan KG, Person RE, Willaert R, Solomon BD, Juusola J.

Genet Med. 2019 Sep;21(9):2036-2042. doi: 10.1038/s41436-019-0454-9. Epub 2019 Feb 11.

PMID:
30739909
31.

Enhancement of the gut barrier integrity by a microbial metabolite through the Nrf2 pathway.

Singh R, Chandrashekharappa S, Bodduluri SR, Baby BV, Hegde B, Kotla NG, Hiwale AA, Saiyed T, Patel P, Vijay-Kumar M, Langille MGI, Douglas GM, Cheng X, Rouchka EC, Waigel SJ, Dryden GW, Alatassi H, Zhang HG, Haribabu B, Vemula PK, Jala VR.

Nat Commun. 2019 Jan 9;10(1):89. doi: 10.1038/s41467-018-07859-7.

32.

Human health risk associated with the management of phosphorus in freshwaters using lanthanum and aluminium.

D'Haese PC, Douglas G, Verhulst A, Neven E, Behets GJ, Vervaet BA, Finsterle K, Lürling M, Spears B.

Chemosphere. 2019 Apr;220:286-299. doi: 10.1016/j.chemosphere.2018.12.093. Epub 2018 Dec 12. Review.

PMID:
30590295
33.

Assessing Ghana's eHealth workforce: implications for planning and training.

Ogoe HA, Asamani JA, Hochheiser H, Douglas GP.

Hum Resour Health. 2018 Nov 27;16(1):65. doi: 10.1186/s12960-018-0330-8.

34.

I've got Toothache, I need Antibiotics: a UK Perspective on Rational Antibiotic Prescribing by Dentists.

Thompson W, Rios LE, Fedorowicz Z, Dailey Y, Douglas G.

Braz Dent J. 2018 Jul-Aug;29(4):395-399. doi: 10.1590/0103-6440201802200.

35.

Lamin B receptor-related disorder is associated with a spectrum of skeletal dysplasia phenotypes.

Thompson E, Abdalla E, Superti-Furga A, McAlister W, Kratz L, Unger S, Royer-Bertrand B, Campos-Xavier B, Mittaz-Crettol L, Amin AK, DeSanto C, Wilson DB, Douglas G, Kozel B, Shinawi M.

Bone. 2019 Mar;120:354-363. doi: 10.1016/j.bone.2018.11.006. Epub 2018 Nov 15.

PMID:
30448303
36.

CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.

Snijders Blok L, Rousseau J, Twist J, Ehresmann S, Takaku M, Venselaar H, Rodan LH, Nowak CB, Douglas J, Swoboda KJ, Steeves MA, Sahai I, Stumpel CTRM, Stegmann APA, Wheeler P, Willing M, Fiala E, Kochhar A, Gibson WT, Cohen ASA, Agbahovbe R, Innes AM, Au PYB, Rankin J, Anderson IJ, Skinner SA, Louie RJ, Warren HE, Afenjar A, Keren B, Nava C, Buratti J, Isapof A, Rodriguez D, Lewandowski R, Propst J, van Essen T, Choi M, Lee S, Chae JH, Price S, Schnur RE, Douglas G, Wentzensen IM, Zweier C, Reis A, Bialer MG, Moore C, Koopmans M, Brilstra EH, Monroe GR, van Gassen KLI, van Binsbergen E, Newbury-Ecob R, Bownass L, Bader I, Mayr JA, Wortmann SB, Jakielski KJ, Strand EA, Kloth K, Bierhals T; DDD study, Roberts JD, Petrovich RM, Machida S, Kurumizaka H, Lelieveld S, Pfundt R, Jansen S, Deriziotis P, Faivre L, Thevenon J, Assoum M, Shriberg L, Kleefstra T, Brunner HG, Wade PA, Fisher SE, Campeau PM.

Nat Commun. 2018 Nov 5;9(1):4619. doi: 10.1038/s41467-018-06014-6. Erratum in: Nat Commun. 2019 Feb 15;10(1):883. Nat Commun. 2019 May 2;10(1):2079.

37.

Correction: TANGO2: expanding the clinical phenotype and spectrum of pathogenic variants.

Dines JN, Golden-Grant K, LaCroix A, Muir AM, Cintrón DL, McWalter K, Cho MT, Sun A, Merritt JL, Thies J, Niyazov D, Burton B, Kim K, Fleming L, Westman R, Karachunski P, Dalton J, Basinger A, Ficicioglu C, Helbig I, Pendziwiat M, Muhle H, Helbig KL, Caliebe A, Santer R, Becker K, Suchy S, Douglas G, Millan F, Begtrup A, Monaghan KG, Mefford HC.

Genet Med. 2019 Aug;21(8):1899. doi: 10.1038/s41436-018-0336-6.

PMID:
30327536
38.

Predicting the Functional Potential of the Microbiome from Marker Genes Using PICRUSt.

Douglas GM, Beiko RG, Langille MGI.

Methods Mol Biol. 2018;1849:169-177. doi: 10.1007/978-1-4939-8728-3_11.

PMID:
30298254
39.

Processing a 16S rRNA Sequencing Dataset with the Microbiome Helper Workflow.

Douglas GM, Comeau AM, Langille MGI.

Methods Mol Biol. 2018;1849:131-141. doi: 10.1007/978-1-4939-8728-3_9.

PMID:
30298252
40.

A Recurrent De Novo Heterozygous COG4 Substitution Leads to Saul-Wilson Syndrome, Disrupted Vesicular Trafficking, and Altered Proteoglycan Glycosylation.

Ferreira CR, Xia ZJ, Clément A, Parry DA, Davids M, Taylan F, Sharma P, Turgeon CT, Blanco-Sánchez B, Ng BG, Logan CV, Wolfe LA, Solomon BD, Cho MT, Douglas G, Carvalho DR, Bratke H, Haug MG, Phillips JB, Wegner J, Tiemeyer M, Aoki K; Undiagnosed Diseases Network; Scottish Genome Partnership, Nordgren A, Hammarsjö A, Duker AL, Rohena L, Hove HB, Ek J, Adams D, Tifft CJ, Onyekweli T, Weixel T, Macnamara E, Radtke K, Powis Z, Earl D, Gabriel M, Russi AHS, Brick L, Kozenko M, Tham E, Raymond KM, Phillips JA 3rd, Tiller GE, Wilson WG, Hamid R, Malicdan MCV, Nishimura G, Grigelioniene G, Jackson A, Westerfield M, Bober MB, Gahl WA, Freeze HH.

Am J Hum Genet. 2018 Oct 4;103(4):553-567. doi: 10.1016/j.ajhg.2018.09.003.

41.

TANGO2: expanding the clinical phenotype and spectrum of pathogenic variants.

Dines JN, Golden-Grant K, LaCroix A, Muir AM, Cintrón DL, McWalter K, Cho MT, Sun A, Merritt JL, Thies J, Niyazov D, Burton B, Kim K, Fleming L, Westman R, Karachunski P, Dalton J, Basinger A, Ficicioglu C, Helbig I, Pendziwiat M, Muhle H, Helbig KL, Caliebe A, Santer R, Becker K, Suchy S, Douglas G, Millan F, Begtrup A, Monaghan KG, Mefford HC.

Genet Med. 2019 Mar;21(3):601-607. doi: 10.1038/s41436-018-0137-y. Epub 2018 Sep 24. Erratum in: Genet Med. 2018 Oct 15;:.

42.

Microbial reduction of nitrate in the presence of zero-valent iron.

Zhang Y, Douglas GB, Kaksonen AH, Cui L, Ye Z.

Sci Total Environ. 2019 Jan 1;646:1195-1203. doi: 10.1016/j.scitotenv.2018.07.112. Epub 2018 Jul 31.

PMID:
30235605
43.

Variations in the provision and cost of oral healthcare in 11 European countries: a case study.

Eaton KA, Ramsdale M, Leggett H, Csikar J, Vinall K, Whelton H, Douglas G.

Int Dent J. 2019 Apr;69(2):130-140. doi: 10.1111/idj.12437. Epub 2018 Sep 19.

44.

User-centered design and usability testing of RxMAGIC: a prescription management and general inventory control system for free clinic dispensaries.

Fisher AM, Mtonga TM, Espino JU, Jonkman LJ, Connor SE, Cappella NK, Douglas GP.

BMC Health Serv Res. 2018 Sep 10;18(1):703. doi: 10.1186/s12913-018-3517-8.

45.

Variable cardiovascular phenotypes associated with SMAD2 pathogenic variants.

Granadillo JL, Chung WK, Hecht L, Corsten-Janssen N, Wegner D, Nij Bijvank SWA, Toler TL, Pineda-Alvarez DE, Douglas G, Murphy JJ, Shimony J, Shinawi M.

Hum Mutat. 2018 Dec;39(12):1875-1884. doi: 10.1002/humu.23627. Epub 2018 Sep 24. Review.

PMID:
30157302
46.

Consumption frequency of added sugars and UK children's dental caries.

Hong J, Whelton H, Douglas G, Kang J.

Community Dent Oral Epidemiol. 2018 Oct;46(5):457-464. doi: 10.1111/cdoe.12413. Epub 2018 Aug 20.

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Denoising the Denoisers: an independent evaluation of microbiome sequence error-correction approaches.

Nearing JT, Douglas GM, Comeau AM, Langille MGI.

PeerJ. 2018 Aug 8;6:e5364. doi: 10.7717/peerj.5364. eCollection 2018.

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Identifying germ cell mutagens using OECD test guideline 488 (transgenic rodent somatic and germ cell gene mutation assays) and integration with somatic cell testing.

Marchetti F, Aardema MJ, Beevers C, van Benthem J, Godschalk R, Williams A, Yauk CL, Young R, Douglas GR.

Mutat Res Genet Toxicol Environ Mutagen. 2018 Aug;832-833:7-18. doi: 10.1016/j.mrgentox.2018.05.021. Epub 2018 May 29. Erratum in: Mutat Res. 2019 Aug;844:70-71.

49.

Simulation of mouse and rat spermatogenesis to inform genotoxicity testing using OECD test guideline 488.

Marchetti F, Aardema M, Beevers C, van Benthem J, Douglas GR, Godschalk R, Yauk CL, Young R, Williams A.

Mutat Res Genet Toxicol Environ Mutagen. 2018 Aug;832-833:19-28. doi: 10.1016/j.mrgentox.2018.05.020. Epub 2018 Jun 1. Erratum in: Mutat Res. 2019 Aug;844:69.

50.

De novo missense variants in MEIS2 recapitulate the microdeletion phenotype of cardiac and palate abnormalities, developmental delay, intellectual disability and dysmorphic features.

Douglas G, Cho MT, Telegrafi A, Winter S, Carmichael J, Zackai EH, Deardorff MA, Harr M, Williams L, Psychogios A, Erwin AL, Grebe T, Retterer K, Juusola J.

Am J Med Genet A. 2018 Sep;176(9):1845-1851. doi: 10.1002/ajmg.a.40368. Epub 2018 Jul 28.

PMID:
30055086

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