Publications 2009
EBV transformation and cell culturing destabilizes DNA methylation in human lymphoblastoid cell lines.
Grafodatskaya D, Choufani S, Ferreira JC, Butcher DT, Lou Y, Zhao C, Scherer SW, Weksberg R. Genomics. 2009 Dec 18. [Epub ahead of print]
PMID: 20005943
Transmission-ratio distortion in the Framingham Heart Study.
Paterson AD, Waggott D, Schillert A, Infante-Rivard C, Bull SB, Yoo YJ, Pinnaduwage D. BMC Proc. 2009 Dec 15;3 Suppl 7:S51.
PMID: 20018044
Using a latent growth curve model for an integrative assessment of the effects of genetic and environmental factors on multiple phenotypes.
Hamid JS, Roslin NM, Paterson AD, Beyene J. BMC Proc. 2009 Dec 15;3 Suppl 7:S44.
PMID: 20018036
Using a higher criticism statistic to detect modest effects in a genome-wide study of rheumatoid arthritis.
Parkhomenko E, Tritchler D, Lemire M, Hu P, Beyene J. BMC Proc. 2009 Dec 15;3 Suppl 7:S40.
PMID: 20018032
Pathway-based analysis of a genome-wide case-control association study of rheumatoid arthritis.
Beyene J, Hu P, Hamid JS, Parkhomenko E, Paterson AD, Tritchler D. BMC Proc. 2009 Dec 15;3 Suppl 7:S128.
PMID: 20017994
Genome-wide association analysis of cardiovascular-related quantitative traits in the Framingham Heart Study.
Roslin NM, Hamid JS, Paterson AD, Beyene J. BMC Proc. 2009 Dec 15;3 Suppl 7:S117.
PMID: 20017982
Genetic Analysis Workshop 16: Strategies for genome-wide association study analyses.
Cupples LA, Beyene J, Bickeböller H, Daw EW, Fallin MD, Gauderman WJ, Ghosh S, Goode EL, Hauser ER, Hinrichs A, Kent JW Jr, Martin LJ, Martinez M, Neuman RJ, Province M, Szymczak S, Wilcox MA, Ziegler A, Maccluer JW, Almasy L. BMC Proc. 2009 Dec 15;3 Suppl 7:S1.
PMID: 20017962
Direct-to-consumer genetic testing: good, bad or benign?
Caulfield T, Ries NM, Ray PN, Shuman C, Wilson B. Clin Genet. 2010 Feb;77(2):101-5. Epub 2009 Nov 21.
PMID: 19968666
Identification of ANKRD11 and ZNF778 as candidate genes for autism and variable cognitive impairment in the novel 16q24.3 microdeletion syndrome.
Willemsen MH, Fernandez BA, Bacino CA, Gerkes E, de Brouwer AP, Pfundt R, Sikkema-Raddatz B, Scherer SW, Marshall CR, Potocki L, van Bokhoven H, Kleefstra T. Eur J Hum Genet. 2009 Nov 18. [Epub ahead of print]
PMID: 19920853
Screening of DNA methylation at the H19 promoter or the distal region of its ICR1 ensures efficient detection of chromosome 11p15 epimutations in Russell-Silver syndrome.
Horike S, Ferreira JC, Meguro-Horike M, Choufani S, Smith AC, Shuman C, Meschino W, Chitayat D, Zackai E, Scherer SW, Weksberg R. Am J Med Genet A. 2009 Nov;149A(11):2415-23.
PMID: 19876907
Computational methods for discovering structural variation with next-generation sequencing.
Medvedev P, Stanciu M, Brudno M. Nat Methods. 2009 Nov;6(11 Suppl):S13-20.
PMID: 9844226
Using the ratio of means as the effect size measure in combining results of microarray experiments.
Hu P, Greenwood CM, Beyene J. BMC Syst Biol. 2009 Nov 5;3:106
PMID: 19891778
Whole genome scanning: resolving clinical diagnosis and management amidst complex data.
Ali-Khan SE, Daar AS, Shuman C, Ray PN, Scherer SW. Pediatr Res. 2009 Oct;66(4):357-63.
PMID: 19531980
Origins and functional impact of copy number variation in the human genome.
Conrad DF, Pinto D, Redon R, Feuk L, Gokcumen O, Zhang Y, Aerts J, Andrews TD, Barnes C, Campbell P, Fitzgerald T, Hu M, Ihm CH, Kristiansson K, Macarthur DG, Macdonald JR, Onyiah I, Pang AW, Robson S, Stirrups K, Valsesia A, Walter K, Wei J; The Wellcome Trust Case Control Consortium, Tyler-Smith C, Carter NP, Lee C, Scherer SW, Hurles ME. Nature. 2009 Oct 7. [Epub ahead of print]
PMID: 19812545
Association between tumor necrosis factor-alpha promoter -308 A/G polymorphism and susceptibility to sepsis and sepsis mortality: a systematic review and meta-analysis.
Teuffel O, Ethier MC, Beyene J, Sung L. Crit Care Med. 2009 Sep 28. [Epub ahead of print]
PMID: 19789454
A report on the 2009 SIG on short read sequencing and algorithms (Short-SIG).
Brudno M, Medvedev P, Stoye J, De La Vega F. Bioinformatics. 2009 Sep 24. [Epub ahead of print]
PMID: 19783529
Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder.
Fernandez BA, Roberts W, Chung B, Weksberg R, Meyn S, Szatmari P, Joseph-George AM, Mackay S, Whitten K, Noble B, Vardy C, Crosbie V, Luscombe S, Tucker E, Turner L, Marshall CR, Scherer SW. J Med Genet. 2009 Sep 24. [Epub ahead of print]
PMID: 19755429
Brachydactyly A-1 mutations restricted to the central region of the N-terminal active fragment of Indian Hedgehog.
Byrnes AM, Racacho L, Grimsey A, Hudgins L, Kwan AC, Sangalli M, Kidd A, Yaron Y, Lau YL, Nikkel SM, Bulman DE. Eur J Hum Genet. 2009 Sep;17(9):1112-20.
PMID: 19277064
Determining relative importance of variables in developing and validating predictive models.
Beyene J, Atenafu EG, Hamid JS, To T, Sung L. BMC Med Res Methodol. 2009 Sep 14;9:64.
PMID: 19751506
Prepublication data sharing.
Toronto International Data Release Workshop Authors, Birney E, Hudson TJ, Green ED, Gunter C, Eddy S, Rogers J, Harris JR, Ehrlich SD, Apweiler R, Austin CP, Berglund L, Bobrow M, Bountra C, Brookes AJ, Cambon-Thomsen A, Carter NP, Chisholm RL, Contreras JL, Cooke RM, Crosby WL, Dewar K, Durbin R, Dyke SO, Ecker JR, El Emam K, Feuk L, Gabriel SB, Gallacher J, Gelbart WM, Granell A, Guarner F, Hubbard T, Jackson SA, Jennings JL, Joly Y, Jones SM, Kaye J, Kennedy KL, Knoppers BM, Kyrpides NC, Lowrance WW, Luo J, MacKay JJ, Martín-Rivera L, McCombie WR, McPherson JD, Miller L, Miller W, Moerman D, Mooser V, Morton CC, Ostell JM, Ouellette BF, Parkhill J, Raina PS, Rawlings C, Scherer SE, Scherer SW, Schofield PN, Sensen CW, Stodden VC, Sussman MR, Tanaka T, Thornton J, Tsunoda T, Valle D, Vuorio EI, Walker NM, Wallace S, Weinstock G, Whitman WB, Worley KC, Wu C, Wu J, Yu J. Nature. 2009 Sep 10;461(7261):168-70.
PMID: 19741685
Gene expression using microarrays in transplant recipients at risk of EBV lymphoproliferation after organ transplantation: preliminary proof-of-concept.
Allen U, Barton M, Beyene J, Hu P, Khodai-Booran N, Hébert D, Dipchand A, Ng V, Solomon M, Grant D, Fecteau A, Ngan B, Read S, Zielenska M, Weitzman S. Pediatr Transplant. 2009 Sep 7. [Epub ahead of print]
PMID: 19735433
Characterization of a de novo translocation t(5;18)(q33.1;q12.1) in an autistic boy identifies a breakpoint close to SH3TC2, ADRB2, and HTR4 on 5q, and within the desmocollin gene cluster on 18q.
Vincent JB, Noor A, Windpassinger C, Gianakopoulos PJ, Schwarzbraun T, Alfred SE, Stachowiak B, Scherer SW, Roberts W, Wagner K, Kroisel PM, Petek E. Am J Med Genet B Neuropsychiatr Genet. 2009 Sep 5;150B(6):817-26.
PMID: 19086034
Maximum likelihood genome assembly.
Medvedev P, Brudno M. J Comput Biol. 2009 Aug;16(8):1101-16.
PMID: 19645596
Genomic variation in a global village: report of the 10th annual Human Genome Variation Meeting 2008.
Brookes AJ, Chanock SJ, Hudson TJ, Peltonen L, Abecasis G, Kwok PY, Scherer SW. Hum Mutat. 2009 Jul;30(7):1134-8.
PMID: 19384970
Shwachman-Bodian Diamond syndrome is a multi-functional protein implicated in cellular stress responses.
Ball HL, Zhang B, Riches JJ, Gandhi R, Li J, Rommens JM, Myers JS. Hum Mol Genet. 2009 Oct 1;18(19):3684-95. Epub 2009 Jul 14.
PMID: 19602484
Heterogeneous effects of fructose on blood lipids in individuals with type 2 diabetes: systematic review and meta-analysis of experimental trials in humans.
Sievenpiper JL, Carleton AJ, Chatha S, Jiang HY, de Souza RJ, Beyene J, Kendall CW, Jenkins DJ. Diabetes Care. 2009 Oct;32(10):1930-7. Epub 2009 Jul 10.
PMID: 19592634
Oral versus intravenous steroids for treatment of relapses in multiple sclerosis.
Burton JM, O'Connor PW, Hohol M, Beyene J. Cochrane Database Syst Rev. 2009 Jul 8;(3):CD006921.
PMID: 19588409
MoDIL: detecting small indels from clone-end sequencing with mixtures of distributions.
Lee S, Hormozdiari F, Alkan C, Brudno M. Nat Methods. 2009 Jul;6(7):473-4.
PMID: 19483690
Identifying concerted evolution and gene conversion in mammalian gene pairs lasting over 100 million years.
Carson AR, Scherer SW. BMC Evol Biol. 2009 Jul 7;9:156.
PMID: 19583854
A meta-analysis of the effect of antibody therapy for the prevention of severe respiratory syncytial virus infection.
Morris SK, Dzolganovski B, Beyene J, Sung L. BMC Infect Dis. 2009 Jul 5;9:106.
PMID: 19575815
Preterm birth and low birth weight among in vitro fertilization singletons: a systematic review and meta-analyses.
McDonald SD, Han Z, Mulla S, Murphy KE, Beyene J, Ohlsson A; Knowledge Synthesis Group. Eur J Obstet Gynecol Reprod Biol. 2009 Oct;146(2):138-48. Epub 2009 Jul 4.
PMID: 19577836
A multivariate growth curve model for ranking genes in replicated time course microarray data.
Hamid JS, Beyene J. Stat Appl Genet Mol Biol. 2009;8(1):Article33. Epub 2009 Jul 1.
PMID: 19572832
Filtering genes for cluster and network analysis.
Tritchler D, Parkhomenko E, Beyene J. BMC Bioinformatics. 2009 Jun 23;10:193.
PMID: 19549335
Copy number variation analysis and sequencing of the X-linked mental retardation gene TSPAN7/TM4SF2 in patients with autism spectrum disorder.
Noor A, Gianakopoulos PJ, Fernandez B, Marshall CR, Szatmari P, Roberts W, Scherer SW, Vincent JB. Psychiatr Genet. 2009 Jun;19(3):154-5.
PMID: 19339915
Bone marrow cells from patients with Shwachman-Diamond syndrome abnormally express genes involved in ribosome biogenesis and RNA processing.
Rujkijyanont P, Adams SL, Beyene J, Dror Y. Br J Haematol. 2009 Jun;145(6):806-15.
PMID: 19438500
Comparison of brachial and carotid artery ultrasound for assessing extent of subclinical atherosclerosis in HIV: a prospective cohort study.
Odueyungbo A, Smieja M, Thabane L, Smaill F, Gough K, Gill J, Anderson T, Elston D, Smith S, Beyene J, Lonn E. AIDS Res Ther. 2009 Jun 11;6:11.
PMID: 19519884
Whole genome scanning: resolving clinical diagnosis and management amidst complex data.
Ali-Khan SE, Daar AS, Shuman C, Ray PN, Scherer SW. Pediatr Res. 2009 Jun 10. [Epub ahead of print]
PMID: 19531980
TNF-alpha-308 G/A polymorphism and responsiveness to TNF-alpha blockade therapy in moderate to severe rheumatoid arthritis: a systematic review and meta-analysis.
O'Rielly DD, Roslin NM, Beyene J, Pope A, Rahman P. Pharmacogenomics J. 2009 Jun;9(3):161-7.
PMID: 19365401
Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes.
Pezzolesi MG, Poznik GD, Mychaleckyj JC, Paterson AD, Barati MT, Klein JB, Ng DP, Placha G, Canani LH, Bochenski J, Waggott D, Merchant ML, Krolewski B, Mirea L, Wanic K, Katavetin P, Kure M, Wolkow P, Dunn JS, Smiles A, Walker WH, Boright AP, Bull SB; DCCT/EDIC Research Group, Doria A, Rogus JJ, Rich SS, Warram JH, Krolewski AS. Diabetes. 2009 Jun;58(6):1403-10.
PMID: 19252134
MoDIL: detecting small indels from clone-end sequencing with mixtures of distributions.
Lee S, Hormozdiari F, Alkan C, Brudno M. Nat Methods. 2009 Jul;6(7):473-4. Epub 2009 May 31.
Family history of renal disease severity predicts the mutated gene in ADPKD.
Barua M, Cil O, Paterson AD, Wang K, He N, Dicks E, Parfrey P, Pei Y. J Am Soc Nephrol. 2009 Aug;20(8):1833-8. Epub 2009 May 14.
PMID: 19443633
Application of biomedical informatics to chronic pediatric diseases: a systematic review.
Moeinedin F, Moineddin R, Jadad AR, Hamid JS, To T, Beyene J. BMC Med Inform Decis Mak. 2009 May 5;9:22.
PMID: 19416540
SHRiMP: accurate mapping of short color-space reads.
Rumble SM, Lacroute P, Dalca AV, Fiume M, Sidow A, Brudno M. PLoS Comput Biol. 2009 May;5(5):e1000386.
PMID: 19461883
Association between hematologic findings and brain injury due to neonatal hypoxic-ischemic encephalopathy.
Shah V, Beyene J, Shah P, Perlman M. Am J Perinatol. 2009 Apr;26(4):295-302.
PMID: 19031351
Hematopoietic colony-stimulating factor priming does not influence survival in acute myeloid leukemia: a meta-analysis of randomized trials.
Sung L, Alibhai SM, Beyene J, Gamis A, Almeida R, Smith S, Aplenc R. Leukemia. 2009 Apr;23(4):811-3.
PMID: 18987652
Multiple whole-genome alignments without a reference organism.
Dubchak I, Poliakov A, Kislyuk A, Brudno M. Genome Res. 2009 Apr;19(4):682-9.
PMID: 19176791
Conservation of core gene expression in vertebrate tissues.
Chan ET, Quon GT, Chua G, Babak T, Trochesset M, Zirngibl RA, Aubin J, Ratcliffe MJ, Wilde A, Brudno M, Morris QD, Hughes TR. J Biol. 2009;8(3):33. Epub 2009 Apr 16.
PMID: 19371447
Multiple recurrent genetic events converge on control of histone lysine methylation in medulloblastoma.
Northcott PA, Nakahara Y, Wu X, Feuk L, Ellison DW, Croul S, Mack S, Kongkham PN, Peacock J, Dubuc A, Ra YS, Zilberberg K, McLeod J, Scherer SW, Sunil Rao J, Eberhart CG, Grajkowska W, Gillespie Y, Lach B, Grundy R, Pollack IF, Hamilton RL, Van Meter T, Carlotti CG, Boop F, Bigner D, Gilbertson RJ, Rutka JT, Taylor MD. Nat Genet. 2009 Apr;41(4):465-72.
PMID: 19270706
>Type 1 diabetes in the BB rat: a polygenic disease.
Wallis RH, Wang K, Marandi L, Hsieh E, Ning T, Chao GY, Sarmiento J, Paterson AD, Poussier P. Diabetes. 2009 Apr;58(4):1007-17.
PMID: 19168599
Copy number variation analysis and sequencing of the X-linked mental retardation gene TSPAN7/TM4SF2 in patients with autism spectrum disorder.
Noor A, Gianakopoulos PJ, Fernandez B, Marshall CR, Szatmari P, Roberts W, Scherer SW, Vincent JB. Psychiatr Genet. 2009 Mar 31. [Epub ahead of print]
PMID: 19339915
A small p-value from an observed data is not evidence of adequate power for future similar-sized studies: a cautionary note.
Atenafu EG, Hamid JS, Stephens D, To T, Beyene J. Contemp Clin Trials. 2009 Mar;30(2):155-7.
PMID: 19063996
Brachydactyly A-1 mutations restricted to the central region of the N-terminal active fragment of Indian Hedgehog.
Byrnes AM, Racacho L, Grimsey A, Hudgins L, Kwan AC, Sangalli M, Kidd A, Yaron Y, Lau YL, Nikkel SM, Bulman DE.Eur J Hum Genet. 2009 Mar 11. [Epub ahead of print]
PMID: 19277064
Multiple recurrent genetic events converge on control of histone lysine methylation in medulloblastoma.
Northcott PA, Nakahara Y, Wu X, Feuk L, Ellison DW, Croul S, Mack S, Kongkham PN, Peacock J, Dubuc A, Ra YS, Zilberberg K, McLeod J, Scherer SW, Sunil Rao J, Eberhart CG, Grajkowska W, Gillespie Y, Lach B, Grundy R, Pollack IF, Hamilton RL, Van Meter T, Carlotti CG, Boop F, Bigner D, Gilbertson RJ, Rutka JT, Taylor MD. Nat Genet. 2009 Apr;41(4):465-72. Epub 2009 Mar 8.
PMID: 19270706
Genomic variation in a global village: Report of the 10th annual Human Genome Variation Meeting 2008.
Brookes AJ, Chanock SJ, Hudson TJ, Peltonen L, Abecasis G, Kwok PY, Scherer SW. Hum Mutat. 2009 Mar 3. [Epub ahead of print]
PMID: 19384970
Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes mellitus.
Pezzolesi MG, Poznik GD, Mychaleckyj JC, Paterson AD, Barati MT, Klein JB, Ng
DP, Placha G, Canani LH, Bochenski J, Waggott D, Merchant ML, Krolewski B, Mirea L, Wanic K, Katavetin P, Kure M, Wolkow P, Dunn JS, Smiles A, Walker WH, Boright AP, Bull SB; DCCT/EDIC Research Group, Doria A, Rogus JJ, Rich SS, Warram JH, Krolewski AS. Diabetes. 2009 Feb 27. [Epub ahead of print]
PMID: 19252134
Association and mutation analyses of 16p11.2 autism candidate genes.
Kumar RA, Marshall CR, Badner JA, Babatz TD, Mukamel Z, Aldinger KA, Sudi J, Brune CW, Goh G, Karamohamed S, Sutcliffe JS, Cook EH, Geschwind DH, Dobyns WB, Scherer SW, Christian SL. PLoS ONE. 2009;4(2):e4582. Epub 2009 Feb 26.
PMID: 19242545
Family-based genetic association study of insulin-like growth factor I microsatellite markers and premenopausal breast cancer risk.
Fehringer G, Boyd NF, Knight JA, Paterson AD, Dite GS, Giles GG, Southey MC, Andrulis IL, Hopper JL, Ozcelik H. Breast Cancer Res Treat. 2009 Feb 20. [Epub ahead of print]
PMID: 19229608
Becker muscular dystrophy caused by an intronic mutation reducing the efficiency of the splice donor site of intron 26 of the dystrophin gene.
Baskin B, Banwell B, Khater RA, Hawkins C, Ray PN. Neuromuscul Disord. 2009 Mar;19(3):189-92. Epub 2009 Feb 18.
PMID: 19230662
The cycle of genome-directed medicine.
Buchanan JA, Carson AR, Chitayat D, Malkin D, Meyn MS, Ray PN, Shuman C, Weksberg R, Scherer SW. Genome Med. 2009 Feb 2;1(2):16. [Epub ahead of print]
PMID: 19341487
Quebec platelet disorder is linked to the urokinase plasminogen activator gene (PLAU) and increases expression of the linked allele in megakaryocytes.
Diamandis M, Paterson AD, Rommens JM, Veljkovic DK, Blavignac J, Bulman DE, Waye JS, Derome F, Rivard GE, Hayward CP. Blood. 2009 Feb 12;113(7):1543-6.
PMID: 18988861
Evidence for pathogenicity of atypical splice mutations in autosomal dominant polycystic kidney disease.
Wang K, Zhao X, Chan S, Cil O, He N, Song X, Paterson AD, Pei Y. Clin J Am Soc Nephrol. 2009 Feb;4(2):442-9.
PMID: 19158373
Indicators of pain in neonates at risk for neurological impairment.
Stevens B, McGrath P, Dupuis A, Gibbins S, Beyene J, Breau L, Camfield C, Finley GA, Franck LS, Howlett A, Johnston C, McKeever P, O'Brien K, Ohlsson A, Yamada J. J Adv Nurs. 2009 Feb;65(2):285-96.
PMID: 19040693
Antenatal steroid therapy for fetal lung maturation: is there an association with childhood asthma?
Pole JD, Mustard CA, To T, Beyene J, Allen AC. J Asthma. 2009 Feb;46(1):47-52.
PMID: 19191137
Mammographic density: a heritable risk factor for breast cancer.
Boyd NF, Martin LJ, Rommens JM, Paterson AD, Minkin S, Yaffe MJ, Stone J, Hopper JL. Methods Mol Biol. 2009;472:343-60. 2009;472:343-60.
PMID: 19107441
Rosiglitazone: can meta-analysis accurately estimate excess cardiovascular risk given the available data? Re-analysis of randomized trials using various methodologic approaches.
Friedrich JO, Beyene J, Adhikari NK. BMC Res Notes. 2009 Jan 10;2:5.
PMID: 19134216
Type 1 diabetes in the BB rat: a polygenic disease.
Wallis RH, Wang K, Marandi L, Hsieh E, Ning T, Chao GY, Sarmiento J, Paterson AD, Poussier P. Diabetes. 2009 Apr;58(4):1007-17. Epub 2009 Jan 23.
PMID: 19168599
Type 1 diabetes in the BB rat: a polygenic disease.
Pei Y, Obaji J, Dupuis A, Paterson AD, Magistroni R, Dicks E, Parfrey P, Cramer B, Coto E, Torra R, San Millan JL, Gibson R, Breuning M, Peters D, J Am Soc Nephrol. 2009 Jan;20(1):205-12.
PMID: 18945943
Race and ancestry in biomedical research: exploring the challenges.
Caulfield T, Fullerton SM, Ali-Khan SE, Arbour L, Burchard EG, Cooper RS, Hardy BJ, Harry S, Hyde-Lay R, Kahn J, Kittles R, Koenig BA, Lee SS, Malinowski M, Ravitsky V, Sankar P, Scherer SW, Séguin B, Shickle D, Suarez-Kurtz G, Daar AS. Genome Med. 2009 Jan 21;1(1):8. [Epub ahead of print]
PMID: 19348695
Sparse canonical correlation analysis with application to genomic data integration.
Parkhomenko E, Tritchler D, Beyene J. Stat Appl Genet Mol Biol. 2009 Jan;8(1):Article 1. Epub 2009 Jan 6.
PMID: 19222376
Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes.
Grant SF, Qu HQ, Bradfield JP, Marchand L, Kim CE, Glessner JT, Grabs R, Taback SP, Frackelton EC, Eckert AW, Annaiah K, Lawson ML, Otieno FG, Santa E, Shaner JL, Smith RM, Skraban R, Imielinski M, Chiavacci RM, Grundmeier RW, Stanley CA, Kirsch SE, Waggott D, Paterson AD, Monos DS; DCCT/EDIC Research Group, Polychronakos C, Hakonarson H. Diabetes. 2009 Jan;58(1):290-5.
PMID: 18840781
Unified criteria for ultrasonographic diagnosis of ADPKD.
Pei Y, Obaji J, Dupuis A, Paterson AD, Magistroni R, Dicks E, Parfrey P, Cramer B, Coto E, Torra R, San Millan JL, Gibson R, Breuning M, Peters D, Ravine D. J Am Soc Nephrol. 2009 Jan;20(1):205-12.
PMID: 18945943