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Items: 1 to 50 of 102

1.

Estimating the Genome-wide Mutation Rate with Three-Way Identity by Descent.

Tian X, Browning BL, Browning SR.

Am J Hum Genet. 2019 Nov 7;105(5):883-893. doi: 10.1016/j.ajhg.2019.09.012. Epub 2019 Oct 3.

PMID:
31587867
2.

Increasing Access to Autism Spectrum Disorder Diagnostic Consultation in Rural and Underserved Communities: Streamlined Evaluation Within Primary Care.

Hine JF, Allin J, Allman A, Black M, Browning B, Ramsey B, Swanson A, Warren ZE, Zawoyski A, Allen W.

J Dev Behav Pediatr. 2020 Jan;41(1):16-22. doi: 10.1097/DBP.0000000000000727.

PMID:
31490843
3.

Genetic history of the population of Crete.

Drineas P, Tsetsos F, Plantinga A, Lazaridis I, Yannaki E, Razou A, Kanaki K, Michalodimitrakis M, Perez-Jimenez F, De Silvestro G, Renda MC, Stamatoyannopoulos JA, Kidd KK, Browning BL, Paschou P, Stamatoyannopoulos G.

Ann Hum Genet. 2019 Nov;83(6):373-388. doi: 10.1111/ahg.12328. Epub 2019 Jun 13.

4.

Prospects for pharmacotherapies to treat alcohol use disorder: an update on recent human studies.

Farokhnia M, Browning BD, Leggio L.

Curr Opin Psychiatry. 2019 Jul;32(4):255-265. doi: 10.1097/YCO.0000000000000519.

PMID:
31107292
5.

Patellofemoral Arthroplasty.

Godshaw B, Kolodychuk N, Williams GK Jr, Browning B, Jones D.

Ochsner J. 2018 Fall;18(3):280-287. doi: 10.31486/toj.18.0009.

6.

A One-Penny Imputed Genome from Next-Generation Reference Panels.

Browning BL, Zhou Y, Browning SR.

Am J Hum Genet. 2018 Sep 6;103(3):338-348. doi: 10.1016/j.ajhg.2018.07.015. Epub 2018 Aug 9.

7.

Genotype Imputation from Large Reference Panels.

Das S, Abecasis GR, Browning BL.

Annu Rev Genomics Hum Genet. 2018 Aug 31;19:73-96. doi: 10.1146/annurev-genom-083117-021602. Epub 2018 May 23. Review.

PMID:
29799802
8.

Ancestry-specific recent effective population size in the Americas.

Browning SR, Browning BL, Daviglus ML, Durazo-Arvizu RA, Schneiderman N, Kaplan RC, Laurie CC.

PLoS Genet. 2018 May 24;14(5):e1007385. doi: 10.1371/journal.pgen.1007385. eCollection 2018 May.

9.

POPdemog: visualizing population demographic history from simulation scripts.

Zhou Y, Tian X, Browning BL, Browning SR.

Bioinformatics. 2018 Aug 15;34(16):2854-2855. doi: 10.1093/bioinformatics/bty184.

10.

Analysis of Human Sequence Data Reveals Two Pulses of Archaic Denisovan Admixture.

Browning SR, Browning BL, Zhou Y, Tucci S, Akey JM.

Cell. 2018 Mar 22;173(1):53-61.e9. doi: 10.1016/j.cell.2018.02.031. Epub 2018 Mar 15.

11.

Genome-wide association study of heart rate and its variability in Hispanic/Latino cohorts.

Kerr KF, Avery CL, Lin HJ, Raffield LM, Zhang QS, Browning BL, Browning SR, Conomos MP, Gogarten SM, Laurie CC, Sofer T, Thornton TA, Hohensee C, Jackson RD, Kooperberg C, Li Y, Méndez-Giráldez R, Perez MV, Peters U, Reiner AP, Zhang ZM, Yao J, Sotoodehnia N, Taylor KD, Guo X, Lange LA, Soliman EZ, Wilson JG, Rotter JI, Heckbert SR, Jain D, Whitsel EA.

Heart Rhythm. 2017 Nov;14(11):1675-1684. doi: 10.1016/j.hrthm.2017.06.018. Epub 2017 Jun 10.

12.

Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos.

Hodonsky CJ, Jain D, Schick UM, Morrison JV, Brown L, McHugh CP, Schurmann C, Chen DD, Liu YM, Auer PL, Laurie CA, Taylor KD, Browning BL, Li Y, Papanicolaou G, Rotter JI, Kurita R, Nakamura Y, Browning SR, Loos RJF, North KE, Laurie CC, Thornton TA, Pankratz N, Bauer DE, Sofer T, Reiner AP.

PLoS Genet. 2017 Apr 28;13(4):e1006760. doi: 10.1371/journal.pgen.1006760. eCollection 2017 Apr.

13.

Genetics of the peloponnesean populations and the theory of extinction of the medieval peloponnesean Greeks.

Stamatoyannopoulos G, Bose A, Teodosiadis A, Tsetsos F, Plantinga A, Psatha N, Zogas N, Yannaki E, Zalloua P, Kidd KK, Browning BL, Stamatoyannopoulos J, Paschou P, Drineas P.

Eur J Hum Genet. 2017 May;25(5):637-645. doi: 10.1038/ejhg.2017.18. Epub 2017 Mar 8.

14.

Genome-wide association of white blood cell counts in Hispanic/Latino Americans: the Hispanic Community Health Study/Study of Latinos.

Jain D, Hodonsky CJ, Schick UM, Morrison JV, Minnerath S, Brown L, Schurmann C, Liu Y, Auer PL, Laurie CA, Taylor KD, Browning BL, Papanicolaou G, Browning SR, Loos RJF, North KE, Thyagarajan B, Laurie CC, Thornton TA, Sofer T, Reiner AP.

Hum Mol Genet. 2017 Mar 15;26(6):1193-1204. doi: 10.1093/hmg/ddx024.

15.

Therapeutic Hypothermia after In-Hospital Cardiac Arrest in Children.

Moler FW, Silverstein FS, Holubkov R, Slomine BS, Christensen JR, Nadkarni VM, Meert KL, Browning B, Pemberton VL, Page K, Gildea MR, Scholefield BR, Shankaran S, Hutchison JS, Berger JT, Ofori-Amanfo G, Newth CJ, Topjian A, Bennett KS, Koch JD, Pham N, Chanani NK, Pineda JA, Harrison R, Dalton HJ, Alten J, Schleien CL, Goodman DM, Zimmerman JJ, Bhalala US, Schwarz AJ, Porter MB, Shah S, Fink EL, McQuillen P, Wu T, Skellett S, Thomas NJ, Nowak JE, Baines PB, Pappachan J, Mathur M, Lloyd E, van der Jagt EW, Dobyns EL, Meyer MT, Sanders RC Jr, Clark AE, Dean JM; THAPCA Trial Investigators.

N Engl J Med. 2017 Jan 26;376(4):318-329. doi: 10.1056/NEJMoa1610493. Epub 2017 Jan 24.

16.

Does the saline load test still have a role in the orthopaedic world? A systematic review of the literature.

Browning BB, Ventimiglia AV, Dixit A, Illical E, Urban WP, Jauregui JJ.

Acta Orthop Traumatol Turc. 2016 Dec;50(6):597-600. doi: 10.1016/j.aott.2016.01.004. Epub 2016 Dec 12. Review.

17.

Robust Inference of Identity by Descent from Exome-Sequencing Data.

Fu W, Browning SR, Browning BL, Akey JM.

Am J Hum Genet. 2016 Nov 3;99(5):1106-1116. doi: 10.1016/j.ajhg.2016.09.011. Epub 2016 Oct 13.

18.

A Multidisciplinary Self-Directed Learning Module Improves Knowledge of a Quality Improvement Instrument: The HEART Pathway.

Hartman ND, Harper EN, Leppert LM, Browning BM, Askew K, Manthey DE, Mahler SA.

J Healthc Qual. 2018 Jan/Feb;40(1):e9-e14. doi: 10.1097/JHQ.0000000000000044.

19.

Consideration of Cosegregation in the Pathogenicity Classification of Genomic Variants.

Jarvik GP, Browning BL.

Am J Hum Genet. 2016 Jun 2;98(6):1077-1081. doi: 10.1016/j.ajhg.2016.04.003. Epub 2016 May 26.

20.

Local Ancestry Inference in a Large US-Based Hispanic/Latino Study: Hispanic Community Health Study/Study of Latinos (HCHS/SOL).

Browning SR, Grinde K, Plantinga A, Gogarten SM, Stilp AM, Kaplan RC, Avilés-Santa ML, Browning BL, Laurie CC.

G3 (Bethesda). 2016 Jun 1;6(6):1525-34. doi: 10.1534/g3.116.028779.

21.

ASAFE: ancestry-specific allele frequency estimation.

Zhang QS, Browning BL, Browning SR.

Bioinformatics. 2016 Jul 15;32(14):2227-9. doi: 10.1093/bioinformatics/btw220. Epub 2016 May 3.

22.

Conversion of a Surgically Arthrodesed Knee to a Total Knee Arthroplasty-Is it Worth it? A Meta-Analysis.

Jauregui JJ, Buitrago CA, Pushilin SA, Browning BB, Mulchandani NB, Maheshwari AV.

J Arthroplasty. 2016 Aug;31(8):1736-41. doi: 10.1016/j.arth.2016.01.027. Epub 2016 Jan 21.

PMID:
26883158
23.

Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino Americans.

Schick UM, Jain D, Hodonsky CJ, Morrison JV, Davis JP, Brown L, Sofer T, Conomos MP, Schurmann C, McHugh CP, Nelson SC, Vadlamudi S, Stilp A, Plantinga A, Baier L, Bien SA, Gogarten SM, Laurie CA, Taylor KD, Liu Y, Auer PL, Franceschini N, Szpiro A, Rice K, Kerr KF, Rotter JI, Hanson RL, Papanicolaou G, Rich SS, Loos RJ, Browning BL, Browning SR, Weir BS, Laurie CC, Mohlke KL, North KE, Thornton TA, Reiner AP.

Am J Hum Genet. 2016 Feb 4;98(2):229-42. doi: 10.1016/j.ajhg.2015.12.003. Epub 2016 Jan 21.

24.

Genetic Diversity and Association Studies in US Hispanic/Latino Populations: Applications in the Hispanic Community Health Study/Study of Latinos.

Conomos MP, Laurie CA, Stilp AM, Gogarten SM, McHugh CP, Nelson SC, Sofer T, Fernández-Rhodes L, Justice AE, Graff M, Young KL, Seyerle AA, Avery CL, Taylor KD, Rotter JI, Talavera GA, Daviglus ML, Wassertheil-Smoller S, Schneiderman N, Heiss G, Kaplan RC, Franceschini N, Reiner AP, Shaffer JR, Barr RG, Kerr KF, Browning SR, Browning BL, Weir BS, Avilés-Santa ML, Papanicolaou GJ, Lumley T, Szpiro AA, North KE, Rice K, Thornton TA, Laurie CC.

Am J Hum Genet. 2016 Jan 7;98(1):165-84. doi: 10.1016/j.ajhg.2015.12.001.

25.

Genotype Imputation with Millions of Reference Samples.

Browning BL, Browning SR.

Am J Hum Genet. 2016 Jan 7;98(1):116-26. doi: 10.1016/j.ajhg.2015.11.020.

26.

Nurses' Attitudes Toward Clinical Research: Experience of the Therapeutic Hypothermia After Pediatric Cardiac Arrest Trials.

Browning B, Page KE, Kuhn RL, DiLiberto MA, Deschenes J, Taillie E, Tomanio E, Holubkov R, Dean JM, Moler FW, Meert K, Pemberton VL.

Pediatr Crit Care Med. 2016 Mar;17(3):e121-9. doi: 10.1097/PCC.0000000000000609.

27.

Accurate Non-parametric Estimation of Recent Effective Population Size from Segments of Identity by Descent.

Browning SR, Browning BL.

Am J Hum Genet. 2015 Sep 3;97(3):404-18. doi: 10.1016/j.ajhg.2015.07.012. Epub 2015 Aug 20.

28.

The Tec Kinase-Regulated Phosphoproteome Reveals a Mechanism for the Regulation of Inhibitory Signals in Murine Macrophages.

Tampella G, Kerns HM, Niu D, Singh S, Khim S, Bosch KA, Garrett ME, Moguche A, Evans E, Browning B, Jahan TA, Nacht M, Wolf-Yadlin A, Plebani A, Hamerman JA, Rawlings DJ, James RG.

J Immunol. 2015 Jul 1;195(1):246-56. doi: 10.4049/jimmunol.1403238. Epub 2015 May 29.

29.

Therapeutic hypothermia after out-of-hospital cardiac arrest in children.

Moler FW, Silverstein FS, Holubkov R, Slomine BS, Christensen JR, Nadkarni VM, Meert KL, Clark AE, Browning B, Pemberton VL, Page K, Shankaran S, Hutchison JS, Newth CJ, Bennett KS, Berger JT, Topjian A, Pineda JA, Koch JD, Schleien CL, Dalton HJ, Ofori-Amanfo G, Goodman DM, Fink EL, McQuillen P, Zimmerman JJ, Thomas NJ, van der Jagt EW, Porter MB, Meyer MT, Harrison R, Pham N, Schwarz AJ, Nowak JE, Alten J, Wheeler DS, Bhalala US, Lidsky K, Lloyd E, Mathur M, Shah S, Wu T, Theodorou AA, Sanders RC Jr, Dean JM; THAPCA Trial Investigators.

N Engl J Med. 2015 May 14;372(20):1898-908. doi: 10.1056/NEJMoa1411480. Epub 2015 Apr 25.

30.

The US Network of Pediatric Multiple Sclerosis Centers: Development, Progress, and Next Steps.

Casper TC, Rose JW, Roalstad S, Waubant E, Aaen G, Belman A, Chitnis T, Gorman M, Krupp L, Lotze TE, Ness J, Patterson M, Rodriguez M, Weinstock-Guttman B, Browning B, Graves J, Tillema JM, Benson L, Harris Y; US Network of Pediatric Multiple Sclerosis Centers.

J Child Neurol. 2015 Sep;30(10):1381-7. doi: 10.1177/0883073814550656. Epub 2014 Sep 30.

31.

Genome-wide haplotypic testing in a Finnish cohort identifies a novel association with low-density lipoprotein cholesterol.

Zhang QS, Browning BL, Browning SR.

Eur J Hum Genet. 2015 May;23(5):672-7. doi: 10.1038/ejhg.2014.105. Epub 2014 Jun 4.

32.

Efficient clustering of identity-by-descent between multiple individuals.

Qian Y, Browning BL, Browning SR.

Bioinformatics. 2014 Apr 1;30(7):915-22. doi: 10.1093/bioinformatics/btt734. Epub 2013 Dec 19.

33.

Large numbers of individuals are required to classify and define risk for rare variants in known cancer risk genes.

Shirts BH, Jacobson A, Jarvik GP, Browning BL.

Genet Med. 2014 Jul;16(7):529-34. doi: 10.1038/gim.2013.187. Epub 2013 Dec 19.

34.

Detecting identity by descent and estimating genotype error rates in sequence data.

Browning BL, Browning SR.

Am J Hum Genet. 2013 Nov 7;93(5):840-51. doi: 10.1016/j.ajhg.2013.09.014. Epub 2013 Oct 24.

35.

Exome sequencing reveals novel rare variants in the ryanodine receptor and calcium channel genes in malignant hyperthermia families.

Kim JH, Jarvik GP, Browning BL, Rajagopalan R, Gordon AS, Rieder MJ, Robertson PD, Nickerson DA, Fisher NA, Hopkins PM.

Anesthesiology. 2013 Nov;119(5):1054-65. doi: 10.1097/ALN.0b013e3182a8a998.

36.

Additive genetic variation in schizophrenia risk is shared by populations of African and European descent.

de Candia TR, Lee SH, Yang J, Browning BL, Gejman PV, Levinson DF, Mowry BJ, Hewitt JK, Goddard ME, O'Donovan MC, Purcell SM, Posthuma D; International Schizophrenia Consortium; Molecular Genetics of Schizophrenia Collaboration, Visscher PM, Wray NR, Keller MC.

Am J Hum Genet. 2013 Sep 5;93(3):463-70. doi: 10.1016/j.ajhg.2013.07.007. Epub 2013 Aug 15.

37.

Rationale, timeline, study design, and protocol overview of the therapeutic hypothermia after pediatric cardiac arrest trials.

Moler FW, Silverstein FS, Meert KL, Clark AE, Holubkov R, Browning B, Slomine BS, Christensen JR, Dean JM.

Pediatr Crit Care Med. 2013 Sep;14(7):e304-15. doi: 10.1097/PCC.0b013e31828a863a.

38.

Improving the accuracy and efficiency of identity-by-descent detection in population data.

Browning BL, Browning SR.

Genetics. 2013 Jun;194(2):459-71. doi: 10.1534/genetics.113.150029. Epub 2013 Mar 27.

39.

Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.

Wu JH, Lemaitre RN, Manichaikul A, Guan W, Tanaka T, Foy M, Kabagambe EK, Djousse L, Siscovick D, Fretts AM, Johnson C, King IB, Psaty BM, McKnight B, Rich SS, Chen YD, Nettleton JA, Tang W, Bandinelli S, Jacobs DR Jr, Browning BL, Laurie CC, Gu X, Tsai MY, Steffen LM, Ferrucci L, Fornage M, Mozaffarian D.

Circ Cardiovasc Genet. 2013 Apr;6(2):171-83. doi: 10.1161/CIRCGENETICS.112.964619. Epub 2013 Jan 29.

40.

Therapeutic hypothermia after pediatric cardiac arrest trials: the vanguard phase experience and implications for other trials.

Pemberton VL, Browning B, Webster A, Dean JM, Moler FW.

Pediatr Crit Care Med. 2013 Jan;14(1):19-26. doi: 10.1097/PCC.0b013e31825b860b.

41.

Identity-by-descent-based heritability analysis in the Northern Finland Birth Cohort.

Browning SR, Browning BL.

Hum Genet. 2013 Feb;132(2):129-38. doi: 10.1007/s00439-012-1230-y. Epub 2012 Sep 29. Erratum in: Hum Genet. 2013 Aug;132(8):957-8.

42.

Identity by descent between distant relatives: detection and applications.

Browning SR, Browning BL.

Annu Rev Genet. 2012;46:617-33. doi: 10.1146/annurev-genet-110711-155534. Epub 2012 Sep 17. Review.

PMID:
22994355
43.

Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.

Patsopoulos NA; Bayer Pharma MS Genetics Working Group; Steering Committees of Studies Evaluating IFNβ-1b and a CCR1-Antagonist; ANZgene Consortium; GeneMSA; International Multiple Sclerosis Genetics Consortium, Esposito F, Reischl J, Lehr S, Bauer D, Heubach J, Sandbrink R, Pohl C, Edan G, Kappos L, Miller D, Montalbán J, Polman CH, Freedman MS, Hartung HP, Arnason BG, Comi G, Cook S, Filippi M, Goodin DS, Jeffery D, O'Connor P, Ebers GC, Langdon D, Reder AT, Traboulsee A, Zipp F, Schimrigk S, Hillert J, Bahlo M, Booth DR, Broadley S, Brown MA, Browning BL, Browning SR, Butzkueven H, Carroll WM, Chapman C, Foote SJ, Griffiths L, Kermode AG, Kilpatrick TJ, Lechner-Scott J, Marriott M, Mason D, Moscato P, Heard RN, Pender MP, Perreau VM, Perera D, Rubio JP, Scott RJ, Slee M, Stankovich J, Stewart GJ, Taylor BV, Tubridy N, Willoughby E, Wiley J, Matthews P, Boneschi FM, Compston A, Haines J, Hauser SL, McCauley J, Ivinson A, Oksenberg JR, Pericak-Vance M, Sawcer SJ, De Jager PL, Hafler DA, de Bakker PI.

Ann Neurol. 2011 Dec;70(6):897-912. doi: 10.1002/ana.22609. Erratum in: Ann Neurol. 2013 Apr;73(4):561.

44.

Performance of genotype imputation for rare variants identified in exons and flanking regions of genes.

Li L, Li Y, Browning SR, Browning BL, Slater AJ, Kong X, Aponte JL, Mooser VE, Chissoe SL, Whittaker JC, Nelson MR, Ehm MG.

PLoS One. 2011;6(9):e24945. doi: 10.1371/journal.pone.0024945. Epub 2011 Sep 19.

45.

Haplotype phasing: existing methods and new developments.

Browning SR, Browning BL.

Nat Rev Genet. 2011 Sep 16;12(10):703-14. doi: 10.1038/nrg3054. Review.

46.

Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.

Lemaitre RN, Tanaka T, Tang W, Manichaikul A, Foy M, Kabagambe EK, Nettleton JA, King IB, Weng LC, Bhattacharya S, Bandinelli S, Bis JC, Rich SS, Jacobs DR Jr, Cherubini A, McKnight B, Liang S, Gu X, Rice K, Laurie CC, Lumley T, Browning BL, Psaty BM, Chen YD, Friedlander Y, Djousse L, Wu JH, Siscovick DS, Uitterlinden AG, Arnett DK, Ferrucci L, Fornage M, Tsai MY, Mozaffarian D, Steffen LM.

PLoS Genet. 2011 Jul;7(7):e1002193. doi: 10.1371/journal.pgen.1002193. Epub 2011 Jul 28.

47.

Population structure can inflate SNP-based heritability estimates.

Browning SR, Browning BL.

Am J Hum Genet. 2011 Jul 15;89(1):191-3; author reply 193-5. doi: 10.1016/j.ajhg.2011.05.025. No abstract available.

48.

A fast, powerful method for detecting identity by descent.

Browning BL, Browning SR.

Am J Hum Genet. 2011 Feb 11;88(2):173-82. doi: 10.1016/j.ajhg.2011.01.010.

49.

Busulfan dosing in children with BMIs ≥ 85% undergoing HSCT: a new optimal strategy.

Browning B, Thormann K, Donaldson A, Halverson T, Shinkle M, Kletzel M.

Biol Blood Marrow Transplant. 2011 Sep;17(9):1383-8. doi: 10.1016/j.bbmt.2011.01.013. Epub 2011 Feb 1.

50.

Objective preoperative measurement of anterior glenoid bone loss: a pilot study of a computer-based method using unilateral 3-dimensional computed tomography.

Nofsinger C, Browning B, Burkhart SS, Pedowitz RA.

Arthroscopy. 2011 Mar;27(3):322-9. doi: 10.1016/j.arthro.2010.09.007. Epub 2010 Dec 31.

PMID:
21195579

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