Genome-Wide Association studies : (Record no. 516021)
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| 000 -LEADER | |
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| fixed length control field | 04876nam a22003498i 4500 |
| 001 - CONTROL NUMBER | |
| control field | CR9781107337459 |
| 003 - CONTROL NUMBER IDENTIFIER | |
| control field | UkCbUP |
| 005 - DATE AND TIME OF LATEST TRANSACTION | |
| control field | 20200124160213.0 |
| 006 - FIXED-LENGTH DATA ELEMENTS--ADDITIONAL MATERIAL CHARACTERISTICS--GENERAL INFORMATION | |
| fixed length control field | m|||||o||d|||||||| |
| 007 - PHYSICAL DESCRIPTION FIXED FIELD--GENERAL INFORMATION | |
| fixed length control field | cr|||||||||||| |
| 008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION | |
| fixed length control field | 130206s2016||||enk o ||1 0|eng|d |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER | |
| International Standard Book Number | 9781107337459 (ebook) |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER | |
| Cancelled/invalid ISBN | 9781107042766 (hardback) |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER | |
| Cancelled/invalid ISBN | 9781107661202 (paperback) |
| 040 ## - CATALOGING SOURCE | |
| Original cataloging agency | UkCbUP |
| Language of cataloging | eng |
| Description conventions | rda |
| Transcribing agency | UkCbUP |
| 050 00 - LIBRARY OF CONGRESS CALL NUMBER | |
| Classification number | RB155 |
| Item number | .G46 2016 |
| 082 00 - DEWEY DECIMAL CLASSIFICATION NUMBER | |
| Classification number | 616/.042 |
| Edition number | 23 |
| 245 00 - TITLE STATEMENT | |
| Title | Genome-Wide Association studies : |
| Remainder of title | from polymorphism to personalized medicine / |
| Statement of responsibility, etc | Edited by Krishnarao Appasani. |
| 264 #1 - Production, Publication, Distribution, Manufacture, and Copyright Notice (R) | |
| Place of production, publication, distribution, manufacture (R) | Cambridge : |
| Name of producer, publisher, distributor, manufacturer (R) | Cambridge University Press, |
| Date of production, publication, distribution, manufacture, or copyright notice | 2016. |
| 300 ## - PHYSICAL DESCRIPTION | |
| Extent | 1 online resource (xxxi, 391 pages) : |
| Other physical details | digital, PDF file(s). |
| 336 ## - Content Type (R) | |
| Content type term (R) | text |
| Content type code (R) | txt |
| Source (NR) | rdacontent |
| 337 ## - Media Type (R) | |
| Media type term (R) | computer |
| Media type code (R) | c |
| Source (NR) | rdamedia |
| 338 ## - Carrier Type (R) | |
| Carrier type term (R) | online resource |
| Carrier type code (R) | cr |
| Source (NR) | rdacarrier |
| 500 ## - GENERAL NOTE | |
| General note | Title from publisher's bibliographic system (viewed on 01 Jan 2016). |
| 505 0# - FORMATTED CONTENTS NOTE | |
| Formatted contents note | Introduction to genome wide association / Krishnarao Appasani and Raghu K. Appasani -- GWAS : a milestone in the road from genotypes to phenotypes / Urko Martinez-Marigorta, Juan Antonio Rodriguez, and Arcadi Navarro -- Introduction to statistical methods in genome-wide association studies / Can Yang, Cong Li, Dongjun Chung, Mengjie Chen, Joel Gelernter, and Hongyu Zhao -- GWAS replicability across time and space / Urko Martinez-Marigorta, Juan Antonio Rodriguez, and Arcadi Navarro -- Genome-wide association studies of body mass index / Tuomas O. Kilpelainen -- Identification of myocardial infarction susceptible genes and their functional analyses / Kouichi Ozaki and Toshihiro Tanaka -- Admixture mapping for disease gene discovery / Randall C. Johnson, Cheryl A. Winkler, and Meredith Yeager -- Genome-wide association analysis in schizophrenia / Sven Stringer, Dorien H. Nieman, Rene S. Kahn, and Eske M. Derks -- Epigenome-wide association studies in neurodevelopmental disorders / Takeo Kubota, Kunio Miyake, and Takae Hirasawa -- Finding SNPs that affect microRNA regulation in disease-associated genomic regions / Laurent F. Thomas and Pal Saetrom -- From linkage to complex associations : the role of GABRA2 as a risk factor for alcohol use / Sandra Villafuerte, Elisa M. Trucco, and Margit Burmeister -- Copy number variation in monozygous twins / Erwin Brosens, K.G. Snoek, D. Veenma, H. Eussen, D. Tibboel, and A. de Klein -- |
| 505 0# - FORMATTED CONTENTS NOTE | |
| Formatted contents note | Haplotypes of CpG-related SNPs and association with DNA methylation patterns / Yiyi Ma, Caren E. Smith, Yu-Chi Lee, Laurence D. Parnell, Chao-Qiang Lai, and Jose M. Ordovas -- eQTL mapping / Mengjie Chen, Can Yang, Cong Li, and Hongyu Zhao -- Next-generation sequencing for rare diseases / Elena Bosch and Ferran Casals -- Next-generation sequencing for complex disorders / Ferran Casals and Elena Bosch -- Chromosomal breakpoints in breast cancer co-localize with differentially methylated regions / Man-Hung Eric Tang, Vinay Varadan, Sitharthan Kamalakaran, Michael Q. Zhang, James Hicks, and Nevenka Dimitrova -- Signaling network analysis of genomic alterations predict breast cancer drug targets / Naif Zaman and Edwin Wang -- Pharmacogenetic studies in pediatric acute myeloid leukemia / Neha S. Bhise, Lata Chauhan, and Jatinder K. Lamba -- Pharmacogenomics of antiretroviral drugs / Chonlaphat Sukasem, Apichaya Puangpetch, and Sadeep Medhasi -- Population stratification and its implications : lessons from genome-wide studies / Sheikh Nizamuddin, Rakesh Tamang, and Kumarasamy Thangaraj -- How to solve genetic disease on a population scale / Barry Merriman -- Economics of personalized medicine / Katherine Payne and Martin Eden. |
| 520 ## - SUMMARY, ETC. | |
| Summary, etc | Over the last twenty years, genome-wide association studies (GWAS) have revealed a great deal about the genetic basis of a wide range of complex diseases and they will undoubtedly continue to have a broad impact as we move to an era of personalised medicine. This authoritative text, written by leaders and innovators from both academia and industry, covers the basic science as well as the clinical, biotechnological and pharmaceutical potential of these methods. With special emphasis given to highlighting pharmacogenomics and population genomics studies using next-generation technology approaches, this is the first book devoted to combining association studies with single nucleotide polymorphisms, copy number variants, haplotypes and expressed quantitative trait loci. A reliable guide for newcomers to the field as well as for experienced scientists, this is a unique resource for anyone interested in how the revolutionary power of genomics can be applied to solve problems in complex disease. |
| 650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name as entry element | Medical genetics. |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Appasani, Krishnarao, |
| Dates associated with a name | 1959- |
| Relator term | editor. |
| 776 08 - ADDITIONAL PHYSICAL FORM ENTRY | |
| Display text | Print version: |
| International Standard Book Number | 9781107042766 |
| 856 40 - ELECTRONIC LOCATION AND ACCESS | |
| Uniform Resource Identifier | <a href="https://doi.org/10.1017/CBO9781107337459">https://doi.org/10.1017/CBO9781107337459</a> |
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