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  • Showing 1-26 of 26 Results
2016
Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci.Liu, C., Kraja AT, Smith JA, Brody JA, Franceschini N., Bis JC, Rice K., Morrison AC, Lu Y., Weiss S., Guo X., Palmas W., Martin LW, Chen YI, Surendran P., Drenos F., Cook JP, Auer PL, Chu AY, Giri A., et al. Nature genetics, 2016/09/12, (2016) Read More / View Supplemental Materials
Abstract
Identification of a Bipolar Disorder Vulnerable Gene CHDH at 3p21.1.Chang, H., Li L., Peng T., Grigoroiu-Serbanescu M., Bergen SE, Landén M., Hultman CM, Forstner AJ, Strohmaier J., Hecker J., Schulze TG, Müller-Myhsok B., Reif A., Mitchell PB, Martin NG, Cichon S., Nöthen MM, Jamain S., Leboyer M., Bellivier F., et al. Molecular neurobiology, 2016/08/25, (2016) Read More / View Supplemental Materials
Abstract
Trans-ethnic Meta-Analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and Insulin.Liu, CT, Raghavan S., Maruthur N., Kabagambe EK, Hong J., Ng MC, Hivert MF, Lu Y., An P., Bentley AR, Drolet AM, Gaulton KJ, Guo X., Armstrong LL, Irvin MR, Li M., Lipovich L., Rybin DV, Taylor KD, Agyemang C., et al. American journal of human genetics, 2016/06/15, (2016) Read More / View Supplemental Materials
Abstract
Genetic Association of Curative and Adverse Reactions to Tyrosine Kinase Inhibitors in Chinese advanced Non-Small Cell Lung Cancer patients.Ruan, Y., Jiang J., Guo L., Li Y., Huang H., Shen L., Luan M., Li M., Du H., Ma C., He L., Zhang X., and Qin S. Scientific reports, 2016/03/18, Volume 6, p.23368, (2016) Read More / View Supplemental Materials
Abstract
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.Pattaro, C., Teumer A., Gorski M., Chu AY, Li M., Mijatovic V., Garnaas M., Tin A., Sorice R., Li Y., Taliun D., Olden M., Foster M., Yang Q., Chen MH, Pers TH, Johnson AD, Ko YA, Fuchsberger C., Tayo B., et al. Nature communications, 2016/01/21, Volume 7, p.10023, (2016) Read More / View Supplemental Materials
Abstract
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition).Klionsky, DJ, Abdelmohsen K., Abe A., Abedin MJ, Abeliovich H., Acevedo Arozena A., Adachi H., Adams CM, Adams PD, Adeli K., Adhihetty PJ, Adler SG, Agam G., Agarwal R., Aghi MK, Agnello M., Agostinis P., Aguilar PV, Aguirre-Ghiso J., Airoldi EM, et al. Autophagy, 2016/01/02, Volume 12, Issue 1, p.1-222, (2016) Read More / View Supplemental Materials
2015
Convergent Lines of Evidence Support LRP8 as a Susceptibility Gene for Psychosis.Li, M., Huang L., Grigoroiu-Serbanescu M., Bergen SE, Landén M., Hultman CM, Forstner AJ, Strohmaier J., Hecker J., Schulze TG, Müller-Myhsok B., Reif A., Mitchell PB, Martin NG, Cichon S., Nöthen MM, Alkelai A., Lerer B., Jamain S., Leboyer M., et al. Molecular neurobiology, 2015/12/04, (2015) Read More / View Supplemental Materials
Abstract
Targeted DNA Sequencing from Autism Spectrum Disorder Brains Implicates Multiple Genetic Mechanisms.D'Gama, AM, Pochareddy S., Li M., Jamuar SS, Reiff RE, Lam AT, Sestan N., and Walsh CA Neuron, 2015/12/02, Volume 88, Issue 5, p.910-7, (2015) Read More / View Supplemental Materials
Abstract
Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci.Gaulton, KJ, Ferreira T., Lee Y., Raimondo A., Mägi R., Reschen ME, Mahajan A., Locke A., William Rayner N., Robertson N., Scott RA, Prokopenko I., Scott LJ, Green T., Sparso T., Thuillier D., Yengo L., Grallert H., Wahl S., Frånberg M., et al. Nature genetics, 2015/11/09, (2015) Read More / View Supplemental Materials
Abstract
Impact of a cis-associated gene expression SNP on chromosome 20q11.22 on bipolar disorder susceptibility, hippocampal structure and cognitive performance.Li, M., Luo XJ, Landén M., Bergen SE, Hultman CM, Li X., Zhang W., Yao YG, Zhang C., Liu J., Mattheisen M., Cichon S., Mühleisen TW, Degenhardt FA, Nöthen MM, Schulze TG, Grigoroiu-Serbanescu M., Li H., Fuller CK, Chen C., et al. The British journal of psychiatry : the journal of mental science, 2015/09/03, (2015) Read More / View Supplemental Materials
Abstract
Association studies of genomic variants with treatment response to risperidone, clozapine, quetiapine and chlorpromazine in the Chinese Han population.Xu, Q., Wu X., Li M., Huang H., Minica C., Yi Z., Wang G., Shen L., Xing Q., Shi Y., He L., and Qin S. The pharmacogenomics journal, 2015/08/18, (2015) Read More / View Supplemental Materials
Abstract
Somatic Cell Fusions Reveal Extensive Heterogeneity in Basal-like Breast Cancer.Su, Y., Subedee A., Bloushtain-Qimron N., Savova V., Krzystanek M., Li L., Marusyk A., Tabassum DP, Zak A., Flacker MJ, Li M., Lin JJ, Sukumar S., Suzuki H., Long H., Szallasi Z., Gimelbrant A., Maruyama R., and Polyak K. Cell reports, 2015/06/16, Volume 11, Issue 10, p.1549-63, (2015) Read More / View Supplemental Materials
Abstract
Advancing Biological Understanding and Therapeutics Discovery with Small-Molecule Probes.Schreiber, SL, Kotz JD, Li M., Aubé J., Austin CP, Reed JC, Rosen H., White EL, Sklar LA, Lindsley CW, Alexander BR, Bittker JA, Clemons PA, De Souza A., Foley MA, Palmer M., Shamji AF, Wawer MJ, McManus O., Wu M., et al. Cell, 2015/06/04, Volume 161, Issue 6, p.1252-1265, (2015) Read More / View Supplemental Materials
Abstract
Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility.Wessel, J., Chu AY, Willems SM, Wang S., Yaghootkar H., Brody JA, Dauriz M., Hivert MF, Raghavan S., Lipovich L., Hidalgo B., Fox K., Huffman JE, An P., Lu Y., Rasmussen-Torvik LJ, Grarup N., Ehm MG, Li L., Baldridge AS, et al. Nature communications, 2015/01/29, Volume 6, p.5897, (2015) Read More / View Supplemental Materials
Abstract
Modulation of genetic associations with serum urate levels by body-mass-index in humans.Huffman, JE, Albrecht E., Teumer A., Mangino M., Kapur K., Johnson T., Kutalik Z., Pirastu N., Pistis G., Lopez LM, Haller T., Salo P., Goel A., Li M., Tanaka T., Dehghan A., Ruggiero D., Malerba G., Smith AV, Nolte IM, et al. PloS one, 2015/01/01, Volume 10, Issue 3, p.e0119752, (2015) Read More / View Supplemental Materials
Abstract
2014
Genome-wide association study of kidney function decline in individuals of European descent.Gorski, M., Tin A., Garnaas M., McMahon GM, Chu AY, Tayo BO, Pattaro C., Teumer A., Chasman DI, Chalmers J., Hamet P., Tremblay J., Woodward M., Aspelund T., Eiriksdottir G., Gudnason V., Harris TB, Launer LJ, Smith AV, Mitchell BD, et al. Kidney international, 2014/12/10, (2014) Read More / View Supplemental Materials
Abstract
Novel loci associated with usual sleep duration: the CHARGE Consortium Genome-Wide Association Study.Gottlieb, DJ, Hek K., Chen TH, Watson NF, Eiriksdottir G., Byrne EM, Cornelis M., Warby SC, Bandinelli S., Cherkas L., Evans DS, Grabe HJ, Lahti J., Li M., Lehtimäki T., Lumley T., Marciante KD, Pérusse L., Psaty BM, Robbins J., et al. Molecular psychiatry, 2014/12/02, (2014) Read More / View Supplemental Materials
Abstract
Novel loci associated with usual sleep duration: the CHARGE Consortium Genome-Wide Association Study.Gottlieb, DJ, Hek K., Chen TH, Watson NF, Eiriksdottir G., Byrne EM, Cornelis M., Warby SC, Bandinelli S., Cherkas L., Evans DS, Grabe HJ, Lahti J., Li M., Lehtimäki T., Lumley T., Marciante KD, Pérusse L., Psaty BM, Robbins J., et al. Molecular psychiatry, 2014/11/18, (2014) Read More / View Supplemental Materials
Polygenic inheritance of paclitaxel-induced sensory peripheral neuropathy driven by axon outgrowth gene sets in CALGB 40101 (Alliance).Chhibber, A., Mefford J., Stahl EA, Pendergrass SA, Baldwin RM, Owzar K., Li M., Winer EP, Hudis CA, Zembutsu H., Kubo M., Nakamura Y., McLeod HL, Ratain MJ, Shulman LN, Ritchie MD, Plenge RM, Witte JS, and Kroetz DL The pharmacogenomics journal, 2014/02/11, (2014) Read More / View Supplemental Materials
Abstract
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks.Peloso, GM, Auer PL, Bis JC, Voorman A., Morrison AC, Stitziel NO, Brody JA, Khetarpal SA, Crosby JR, Fornage M., Isaacs A., Jakobsdottir J., Feitosa MF, Davies G., Huffman JE, Manichaikul A., Davis B., Lohman K., Joon AY, Smith AV, et al. American journal of human genetics, 2014/02/06, Volume 94, Issue 2, p.223-32, (2014) Read More / View Supplemental Materials
Abstract
2013
High-throughput genetic screen for synaptogenic factors: identification of LRP6 as critical for excitatory synapse development.Sharma, K., Choi SY, Zhang Y., Nieland TJ, Long S., Li M., and Huganir RL Cell reports, 2013/12/12, Volume 5, Issue 5, p.1330-41, (2013) Read More / View Supplemental Materials
Abstract
2012
Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study.Voight, BF, Peloso GM, Orho-Melander M., Frikke-Schmidt R., Barbalic M., Jensen MK, Hindy G., Hólm H., Ding EL, Johnson T., Schunkert H., Samani NJ, Clarke R., Hopewell JC, Thompson JF, Li M., Thorleifsson G., Newton-Cheh C., Musunuru K., Pirruccello JP, et al. Lancet, 2012/05/17, (2012) Read More / View Supplemental Materials
Abstract
Large-Scale Gene-Centric Meta-Analysis across 39 Studies Identifies Type 2 Diabetes Loci.Saxena, R., Elbers CC, Guo Y., Peter I., Gaunt TR, Mega JL, Lanktree MB, Tare A., Castillo BA, Li YR, Johnson T., Bruinenberg M., Gilbert-Diamond D., Rajagopalan R., Voight BF, Balasubramanyam A., Barnard J., Bauer F., Baumert J., Bhangale T., et al. American journal of human genetics, 2012/03/09, Volume 90, Issue 3, p.410-425, (2012) Read More / View Supplemental Materials
Abstract
The NIH's role in accelerating translational sciences.Reed, JC, White EL, Aubé J., Lindsley C., Li M., Sklar L., and Schreiber S. Nature biotechnology, 2012/01/09, Volume 30, Issue 1, p.16-9, (2012) Read More / View Supplemental Materials
2010
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.Voight, BF, Scott LJ, Steinthorsdottir V., Morris AP, Dina C., Welch RP, Zeggini E., Huth C., Aulchenko YS, Thorleifsson G., McCulloch LJ, Ferreira T., Grallert H., Amin N., Wu G., Willer CJ, Raychaudhuri S., McCarroll SA, Langenberg C., Hofmann OM, et al. Nature genetics, 2010/07/01, Volume 42, Issue 7, p.579-89, (2010) Read More / View Supplemental Materials
Abstract
Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge.Saxena, R., Hivert MF, Langenberg C., Tanaka T., Pankow JS, Vollenweider P., Lyssenko V., Bouatia-Naji N., Dupuis J., Jackson AU, Kao WH, Li M., Glazer NL, Manning AK, Luan J., Stringham HM, Prokopenko I., Johnson T., Grarup N., Boesgaard TW, et al. Nature genetics, 2010/02/01, Volume 42, Issue 2, p.142-8, (2010) Read More / View Supplemental Materials
Abstract
  • Showing 1-26 of 26 Results