Literature DB >> 11037314

Definition of the phenotype.

J P Rice1, N L Saccone, E Rasmussen.   

Abstract

Definition of the phenotype is a key issue in designing any genetic study whose goal is to detect disease genes. This chapter describes strategies to increase the power to detect susceptibility loci for complex diseases. A narrowly defined disease phenotype can offer advantages over broad definitions. Studies of clinical disease can also benefit from judicious selection of endophenotypes and related quantitative traits for analysis. The effect of diagnostic and measurement error is also discussed; power is maximized when strategies to reduce error are incorporated into a study design.

Mesh:

Year:  2001        PMID: 11037314     DOI: 10.1016/s0065-2660(01)42015-3

Source DB:  PubMed          Journal:  Adv Genet        ISSN: 0065-2660            Impact factor:   1.944


  25 in total

1.  Pleiotropic effects of a chromosome 3 locus on speech-sound disorder and reading.

Authors:  Catherine M Stein; James H Schick; H Gerry Taylor; Lawrence D Shriberg; Christopher Millard; Amy Kundtz-Kluge; Karlie Russo; Nori Minich; Amy Hansen; Lisa A Freebairn; Robert C Elston; Barbara A Lewis; Sudha K Iyengar
Journal:  Am J Hum Genet       Date:  2004-01-20       Impact factor: 11.025

2.  Genomewide rapid association using mixed model and regression: a fast and simple method for genomewide pedigree-based quantitative trait loci association analysis.

Authors:  Yurii S Aulchenko; Dirk-Jan de Koning; Chris Haley
Journal:  Genetics       Date:  2007-07-29       Impact factor: 4.562

Review 3.  Genetics of the Framingham Heart Study population.

Authors:  Diddahally R Govindaraju; L Adrienne Cupples; William B Kannel; Christopher J O'Donnell; Larry D Atwood; Ralph B D'Agostino; Caroline S Fox; Marty Larson; Daniel Levy; Joanne Murabito; Ramachandran S Vasan; Greta Lee Splansky; Philip A Wolf; Emelia J Benjamin
Journal:  Adv Genet       Date:  2008       Impact factor: 1.944

4.  Identification of Phenotypes in People with COPD: Influence of Physical Activity, Sedentary Behaviour, Body Composition and Skeletal Muscle Strength.

Authors:  Rafaella F Xavier; Ana Carolina A C Pereira; Aline C Lopes; Vinícius Cavalheri; Regina M C Pinto; Alberto Cukier; Ercy M C Ramos; Celso R F Carvalho
Journal:  Lung       Date:  2018-11-14       Impact factor: 2.584

5.  Validation of electronic medical record-based phenotyping algorithms: results and lessons learned from the eMERGE network.

Authors:  Katherine M Newton; Peggy L Peissig; Abel Ngo Kho; Suzette J Bielinski; Richard L Berg; Vidhu Choudhary; Melissa Basford; Christopher G Chute; Iftikhar J Kullo; Rongling Li; Jennifer A Pacheco; Luke V Rasmussen; Leslie Spangler; Joshua C Denny
Journal:  J Am Med Inform Assoc       Date:  2013-03-26       Impact factor: 4.497

6.  Association between AVPR1A, DRD2, and ASPM and endophenotypes of communication disorders.

Authors:  Catherine M Stein; Barbara Truitt; Fenghua Deng; Allison Avrich Ciesla; Feiyou Qiu; Peronne Joseph; Rekha Raghavendra; Jeremy Fondran; Robert P Igo; Jessica Tag; Lisa Freebairn; H Gerry Taylor; Barbara A Lewis; Sudha K Iyengar
Journal:  Psychiatr Genet       Date:  2014-10       Impact factor: 2.458

7.  Database queries for hospitalizations for acute congestive heart failure: flexible methods and validation based on set theory.

Authors:  Marc Rosenman; Jinghua He; Joel Martin; Kavitha Nutakki; George Eckert; Kathleen Lane; Irmina Gradus-Pizlo; Siu L Hui
Journal:  J Am Med Inform Assoc       Date:  2013-10-10       Impact factor: 4.497

Review 8.  Genomic variants, genes, and pathways of Alzheimer's disease: An overview.

Authors:  Adam C Naj; Gerard D Schellenberg
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2017-01       Impact factor: 3.568

Review 9.  A testable prognostic model of nicotine dependence.

Authors:  Rachel Badovinac Ramoni; Nancy L Saccone; Dorothy K Hatsukami; Laura J Bierut; Marco F Ramoni
Journal:  J Neurogenet       Date:  2009-01-31       Impact factor: 1.250

10.  Otitis media: a genome-wide linkage scan with evidence of susceptibility loci within the 17q12 and 10q22.3 regions.

Authors:  Margaretha L Casselbrant; Ellen M Mandel; Jeesun Jung; Robert E Ferrell; Kathleen Tekely; Jin P Szatkiewicz; Amrita Ray; Daniel E Weeks
Journal:  BMC Med Genet       Date:  2009-09-03       Impact factor: 2.103

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