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1 Diagnostic odyssey of patients with mitochondrial disease: Results of a survey

Author(s):
Grier, Johnston; Hirano, Michio; Karaa, Amel; Shepard, Emma; Thompson, John L.
Date:
2018
Subject:
Neurology, Genetics, Mitochondrial pathology, Biometry
Content Type:
Articles
Persistent URL:

2 A New Estimating Equation Based Approach for Secondary Trait Analyses in Genetic Case-control Studies

Author(s):
Song, Xiaoyu
Date:
2015
Subject:
Biometry, Genetics, Case-control method, Generalized estimating equations
Content Type:
Theses
Persistent URL:

3 Phenotypic and molecular analyses of primary lateral sclerosis

Author(s):
Mitsumoto, Hiroshi; Nagy, Peter L.; Gennings, Chris; Murphy, Jennifer; Andrews, Howard F.; Goetz, Raymond R.; Floeter, Mary Kay; Hupf, Jonathan; Singleton, Jessica; Barohn, Richard J.; Nations, Sharon; Shoesmith, Christen; Kasarskis, Edward; Factor-Litvak, Pam; The PLS COSMOS Study Group
Date:
2015
Subject:
Neurology, Genetics, Amyotrophic lateral sclerosis, Motor neurons--Diseases
Content Type:
Articles
Persistent URL:

4 A Rare HBV Subgenotype D4 with Unique Genomic Signatures Identified in North-Eastern India –An Emerging Clinical Challenge?

Author(s):
Banerjee, Priyanka; Mondal, Rajiv Kumar; Nandi, Madhuparna; Ghosh, Sumantra; Khatun, Mousumi; Chakraborty, Nabendu; Bhattacharya, Swatilekha; RoyChoudhury, Arindam; Banerjee, Soma; Santra, Amal; Sil, Samir; Chowdhury, Abhijit; Bhaumik, Pradip; Datta, Simanti
Date:
2014
Subject:
Nucleotide sequence, Phylogeny--Molecular aspects, Hepatitis B virus, Epidemiology, Genetics, Medical sciences
Content Type:
Articles
Publisher:
Public Library of Science
Persistent URL:

5 Comparing the power of family-based association tests for sequence data with applications in the GAW18 simulated data

Author(s):
Huang, Jing; Chen, Yong; Swartz, Michael; Ionita-Laza, Iuliana
Date:
2014
Subject:
Human genetics--Variation, Biometry, Genetics
Content Type:
Articles
Persistent URL:

6 Identification of Rare Causal Variants in Sequence-Based Studies: Methods and Applications to VPS13B, a Gene Involved in Cohen Syndrome and Autism

Author(s):
Ionita-Laza, Iuliana; Capanu, Marinela; De Rubeis, Silvia; McCallum, Kenneth; Buxbaum, Joseph D.
Date:
2014
Subject:
Genetic disorders, Human genetics--Variation, Autism, Genetics, Biometry
Content Type:
Articles
Publisher:
Public Library of Science
Persistent URL:

7 Small sample properties of rare variant analysis methods

Author(s):
Swartz, Michael; Kim, Taebeom; Niu, Jiangong; Yu, Robert; Shete, Sanjay; Ionita-Laza, Iuliana
Date:
2014
Subject:
Human genetics--Variation, Biometry, Genetics
Content Type:
Articles
Persistent URL:

8 A method to identify differential expression profiles of time-course gene data with Fourier transformation

Author(s):
Kim, Jaehee; Ogden, Robert T.; Kim, Haseong
Date:
2013
Subject:
Gene expression--Data processing, Genetics--Data processing, Fourier analysis, Bioinformatics, Gene expression, Genetics, Biology
Content Type:
Articles
Persistent URL:

9 Association analysis of complex diseases using triads, parent-child dyads and singleton monads

Author(s):
Fan, Ruzong; Lee, Annie Jehe; Lu, Zhaohui; Liu, Aiyi; Troendle, James; Mills, James
Date:
2013
Subject:
Medical genetics, Genetic markers, Familial diseases, Association schemes (Combinatorial analysis), Medicine, Biometry, Genetics
Content Type:
Articles
Publisher:
BioMed Central
Persistent URL:

10 Rare Variant Analysis for Family-Based Design

Author(s):
De, Gourab; Yip, Wai-Ki; Ionita-Laza, Iuliana; Laird, Nan
Date:
2013
Subject:
Biometry, Genetics
Content Type:
Articles
Publisher:
Public Library of Science
Persistent URL:

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