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Search life-sciences literature (45,105,671 articles, preprints and more)

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nf-core/airrflow: An adaptive immune receptor repertoire analysis workflow employing the Immcantation framework.
Gabernet G, Marquez S, Bjornson R, Peltzer A, Meng H, Aron E, Lee NY, Jensen CG, Ladd D, Polster M, Hanssen F, Heumos S, nf-core community, Yaari G, Kowarik MC, Nahnsen S, Kleinstein SH
PLoS Comput Biol, 20(7):e1012265, 26 Jul 2024
Cited by: 1 article | PMID: 39058741 | PMCID: PMC11305553
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nf-core/airrflow: an adaptive immune receptor repertoire analysis workflow employing the Immcantation framework
Gabernet G, Marquez S, Bjornson R, Peltzer A, Meng H, Aron E, Lee NY, Jensen C, Ladd D, Hanssen F, Heumos S, nf-core community, Yaari G, Kowarik MC, Nahnsen S, Kleinstein SH
bioRxiv, 20 Jan 2024
Cited by: 0 articles | PPR: PPR790394
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Experimental Evolution of the TolC-Receptor Phage U136B Functionally Identifies a Tail Fiber Protein Involved in Adsorption through Strong Parallel Adaptation.
Burmeister AR, Tzintzun-Tapia E, Roush C, Mangal I, Barahman R, Bjornson RD, Turner PE
Appl Environ Microbiol, 89(6):e0007923, 16 May 2023
Cited by: 5 articles | PMID: 37191555 | PMCID: PMC10304864
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Using blockchain to log genome dataset access: efficient storage and query.
Gürsoy G, Bjornson R, Green ME, Gerstein M
BMC Med Genomics, 13(suppl 7):78, 21 Jul 2020
Cited by: 9 articles | PMID: 32693796 | PMCID: PMC7372787
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De Novo Mutation in Genes Regulating Neural Stem Cell Fate in Human Congenital Hydrocephalus.
Furey CG, Choi J, Jin SC, Zeng X, Timberlake AT, Nelson-Williams C, Mansuri MS, Lu Q, Duran D, Panchagnula S, Allocco A, Karimy JK, Khanna A, Gaillard JR, DeSpenza T, Antwi P, Loring E, Butler WE, Smith ER, [...] Kahle KT
Neuron, 99(2):302-314.e4, 05 Jul 2018
Cited by: 74 articles | PMID: 29983323 | PMCID: PMC7839075
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Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands.
Jin SC, Homsy J, Zaidi S, Lu Q, Morton S, DePalma SR, Zeng X, Qi H, Chang W, Sierant MC, Hung WC, Haider S, Zhang J, Knight J, Bjornson RD, Castaldi C, Tikhonoa IR, Bilguvar K, Mane SM, [...] Brueckner M
Nat Genet, 49(11):1593-1601, 09 Oct 2017
Cited by: 442 articles | PMID: 28991257 | PMCID: PMC5675000
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Large-Scale trans-eQTLs Affect Hundreds of Transcripts and Mediate Patterns of Transcriptional Co-regulation.
Brynedal B, Choi J, Raj T, Bjornson R, Stranger BE, Neale BM, Voight BF, Cotsapas C
Am J Hum Genet, 100(4):581-591, 09 Mar 2017
Cited by: 45 articles | PMID: 28285767 | PMCID: PMC5384037
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Korean Variant Archive (KOVA): a reference database of genetic variations in the Korean population.
Lee S, Seo J, Park J, Nam JY, Choi A, Ignatius JS, Bjornson RD, Chae JH, Jang IJ, Lee S, Park WY, Baek D, Choi M
Sci Rep, 7(1):4287, 27 Jun 2017
Cited by: 42 articles | PMID: 28655895 | PMCID: PMC5487339
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Large-scaletrans-eQTLs affect hundreds of transcripts and mediate patterns of transcriptional co-regulation Short:trans-eQTLs reveal patterns of transcriptional co-regulation
Brynedal B, Choi J, Raj T, Bjornson R, Stranger BE, Neale BM, Voight BF, Cotsapas C
bioRxiv, 31 May 2016
Cited by: 0 articles | PPR: PPR28856
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Genomic landscape of cutaneous T cell lymphoma.
Choi J, Goh G, Walradt T, Hong BS, Bunick CG, Chen K, Bjornson RD, Maman Y, Wang T, Tordoff J, Carlson K, Overton JD, Liu KJ, Lewis JM, Devine L, Barbarotta L, Foss FM, Subtil A, Vonderheid EC, [...] Lifton RP
Nat Genet, 47(9):1011-1019, 20 Jul 2015
Cited by: 235 articles | PMID: 26192916 | PMCID: PMC4552614
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YPED: an integrated bioinformatics suite and database for mass spectrometry-based proteomics research.
Colangelo CM, Shifman M, Cheung KH, Stone KL, Carriero NJ, Gulcicek EE, Lam TT, Wu T, Bjornson RD, Bruce C, Nairn AC, Rinehart J, Miller PL, Williams KR
Genomics Proteomics Bioinformatics, 13(1):25-35, 21 Feb 2015
Cited by: 8 articles | PMID: 25712262 | PMCID: PMC4411476
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A spatial simulation approach to account for protein structure when identifying non-random somatic mutations.
Ryslik GA, Cheng Y, Cheung KH, Bjornson RD, Zelterman D, Modis Y, Zhao H
BMC Bioinformatics, 15:231, 03 Jul 2014
Cited by: 14 articles | PMID: 24990767 | PMCID: PMC4227039
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Development of a novel method to create double-strand break repair fingerprints using next-generation sequencing.
Soong CP, Breuer GA, Hannon RA, Kim SD, Salem AF, Wang G, Yu R, Carriero NJ, Bjornson R, Sundaram RK, Bindra RS
DNA Repair (Amst), 26:44-53, 19 Dec 2014
Cited by: 11 articles | PMID: 25547252
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Comparative genomics reveals multiple genetic backgrounds of human pathogenicity in the Trypanosoma brucei complex.
Sistrom M, Evans B, Bjornson R, Gibson W, Balmer O, Mäser P, Aksoy S, Caccone A
Genome Biol Evol, 6(10):2811-2819, 05 Oct 2014
Cited by: 28 articles | PMID: 25287146 | PMCID: PMC4224348
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Comparative Genomics Reveals Multiple Genetic Backgrounds of Human Pathogenicity in the Trypanosoma brucei Complex
Sistrom M, Evans B, Bjornson R, Gibson W, Balmer O, Mäser P, Aksoy S, Caccone A
Genome biology and evolution., 6(10):2811-2819, 01 Oct 2014
Cited by: 0 articles | AGR: IND601178032
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Identification of PLX4032-resistance mechanisms and implications for novel RAF inhibitors.
Choi J, Landrette SF, Wang T, Evans P, Bacchiocchi A, Bjornson R, Cheng E, Stiegler AL, Gathiaka S, Acevedo O, Boggon TJ, Krauthammer M, Halaban R, Xu T
Pigment Cell Melanoma Res, 27(2):253-262, 06 Jan 2014
Cited by: 34 articles | PMID: 24283590 | PMCID: PMC4065135
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Low-copy piggyBac transposon mutagenesis in mice identifies genes driving melanoma.
Ni TK, Landrette SF, Bjornson RD, Bosenberg MW, Xu T
Proc Natl Acad Sci U S A, 110(38):E3640-9, 03 Sep 2013
Cited by: 23 articles | PMID: 24003131 | PMCID: PMC3780872
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De novo mutations in histone-modifying genes in congenital heart disease.
Zaidi S, Choi M, Wakimoto H, Ma L, Jiang J, Overton JD, Romano-Adesman A, Bjornson RD, Breitbart RE, Brown KK, Carriero NJ, Cheung YH, Deanfield J, DePalma S, Fakhro KA, Glessner J, Hakonarson H, Italia MJ, Kaltman JR, [...] Lifton RP
Nature, 498(7453):220-223, 12 May 2013
Cited by: 579 articles | PMID: 23665959 | PMCID: PMC3706629
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The functional spectrum of low-frequency coding variation.
Marth GT, Yu F, Indap AR, Garimella K, Gravel S, Leong WF, Tyler-Smith C, Bainbridge M, Blackwell T, Zheng-Bradley X, Chen Y, Challis D, Clarke L, Ball EV, Cibulskis K, Cooper DN, Fulton B, Hartl C, Koboldt D, [...] 1000 Genomes Project
Genome Biol, 12(9):R84, 14 Sep 2011
Cited by: 146 articles | PMID: 21917140 | PMCID: PMC3308047
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Variation in genome-wide mutation rates within and between human families.
Conrad DF, Keebler JE, DePristo MA, Lindsay SJ, Zhang Y, Casals F, Idaghdour Y, Hartl CL, Torroja C, Garimella KV, Zilversmit M, Cartwright R, Rouleau GA, Daly M, Stone EA, Hurles ME, Awadalla P, 1000 Genomes Project
Nat Genet, 43(7):712-714, 12 Jun 2011
Cited by: 344 articles | PMID: 21666693 | PMCID: PMC3322360
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De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
Sanders SJ, Murtha MT, Gupta AR, Murdoch JD, Raubeson MJ, Willsey AJ, Ercan-Sencicek AG, DiLullo NM, Parikshak NN, Stein JL, Walker MF, Ober GT, Teran NA, Song Y, El-Fishawy P, Murtha RC, Choi M, Overton JD, Bjornson RD, [...] State MW
Nature, 485(7397):237-241, 04 Apr 2012
Cited by: 1272 articles | PMID: 22495306 | PMCID: PMC3667984
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Demographic history and rare allele sharing among human populations.
Gravel S, Henn BM, Gutenkunst RN, Indap AR, Marth GT, Clark AG, Yu F, Gibbs RA, 1000 Genomes Project, Bustamante CD
Proc Natl Acad Sci U S A, 108(29):11983-11988, 05 Jul 2011
Cited by: 388 articles | PMID: 21730125 | PMCID: PMC3142009
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The 1000 Genomes Project: data management and community access.
Clarke L, Zheng-Bradley X, Smith R, Kulesha E, Xiao C, Toneva I, Vaughan B, Preuss D, Leinonen R, Shumway M, Sherry S, Flicek P, 1000 Genomes Project Consortium
Nat Methods, 9(5):459-462, 27 Apr 2012
Cited by: 221 articles | PMID: 22543379 | PMCID: PMC3340611
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Insight into the transmission biology and species-specific functional capabilities of tsetse (Diptera: glossinidae) obligate symbiont Wigglesworthia.
Rio RV, Symula RE, Wang J, Lohs C, Wu YN, Snyder AK, Bjornson RD, Oshima K, Biehl BS, Perna NT, Hattori M, Aksoy S
mBio, 3(1):e00240-11, 14 Feb 2012
Cited by: 68 articles | PMID: 22334516 | PMCID: PMC3280448
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Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities.
Boyden LM, Choi M, Choate KA, Nelson-Williams CJ, Farhi A, Toka HR, Tikhonova IR, Bjornson R, Mane SM, Colussi G, Lebel M, Gordon RD, Semmekrot BA, Poujol A, Välimäki MJ, De Ferrari ME, Sanjad SA, Gutkin M, Karet FE, [...] Lifton RP
Nature, 482(7383):98-102, 22 Jan 2012
Cited by: 384 articles | PMID: 22266938 | PMCID: PMC3278668
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1-25 of 53 results

1 2 3

Search life-sciences literature (45,105,671 articles, preprints and more)

Search results

nf-core/airrflow: An adaptive immune receptor repertoire analysis workflow employing the Immcantation framework.

nf-core/airrflow: an adaptive immune receptor repertoire analysis workflow employing the Immcantation framework

Experimental Evolution of the TolC-Receptor Phage U136B Functionally Identifies a Tail Fiber Protein Involved in Adsorption through Strong Parallel Adaptation.

Using blockchain to log genome dataset access: efficient storage and query.

De Novo Mutation in Genes Regulating Neural Stem Cell Fate in Human Congenital Hydrocephalus.

Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands.

Large-Scale trans-eQTLs Affect Hundreds of Transcripts and Mediate Patterns of Transcriptional Co-regulation.

Korean Variant Archive (KOVA): a reference database of genetic variations in the Korean population.

Large-scaletrans-eQTLs affect hundreds of transcripts and mediate patterns of transcriptional co-regulation Short:trans-eQTLs reveal patterns of transcriptional co-regulation

Genomic landscape of cutaneous T cell lymphoma.

YPED: an integrated bioinformatics suite and database for mass spectrometry-based proteomics research.

A spatial simulation approach to account for protein structure when identifying non-random somatic mutations.

Development of a novel method to create double-strand break repair fingerprints using next-generation sequencing.

Comparative genomics reveals multiple genetic backgrounds of human pathogenicity in the Trypanosoma brucei complex.

Comparative Genomics Reveals Multiple Genetic Backgrounds of Human Pathogenicity in the Trypanosoma brucei Complex

Identification of PLX4032-resistance mechanisms and implications for novel RAF inhibitors.

Low-copy piggyBac transposon mutagenesis in mice identifies genes driving melanoma.

De novo mutations in histone-modifying genes in congenital heart disease.

The functional spectrum of low-frequency coding variation.

Variation in genome-wide mutation rates within and between human families.

De novo mutations revealed by whole-exome sequencing are strongly associated with autism.

Demographic history and rare allele sharing among human populations.

The 1000 Genomes Project: data management and community access.

Insight into the transmission biology and species-specific functional capabilities of tsetse (Diptera: glossinidae) obligate symbiont Wigglesworthia.

Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities.

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