J. Graham

发表

Alzheimer ’ s Disease Neuroimaging Initiativea Multivariate association between single-nucleotide polymorphisms in Alzgene linkage regions and structural changes in the brain : discovery , refinement and validation

M. Beg, F. Nathoo, E. Szefer, 2017 .

Single-Nucleotide Polymorphisms in Aldo-Keto and Carbonyl Reductase Genes Are Not Associated with Acute Cardiotoxicity after Daunorubicin Chemotherapy

J. Graham, T. Grigliatti, J. Lubieniecka, 2012, Cancer Epidemiology, Biomarkers & Prevention.

Gene genealogies for genetic association mapping, with application to Crohn's disease

C. Greenwood, J. Graham, K. Burkett, 2013, Front. Genet..

Cost–Effective Prediction of Gender-Labeling Errors and Estimation of Gender-Labeling Error Rates in Candidate-Gene Association Studies

Conghui Qu, Jinko Graham, Angela Brooks-Wilson, 2011, Front. Gene..

Using gene genealogies to localize rare variants associated with complex traits in diploid populations

Charith B. Karunarathna, J. Graham, 2017, bioRxiv.

MHC Class I Chain‐Related Gene‐A Is Associated with IA2 and IAA but Not GAD in Swedish Type 1 Diabetes Mellitus

Å. Lernmark, W. Hagopian, J. Graham, 2006, Annals of the New York Academy of Sciences.

Case-Control Inference of Interaction between Genetic and Nongenetic Risk Factors under Assumptions on Their Distribution

J. Graham, Ji-Hyung Shin, B. McNeney, 2007, Statistical applications in genetics and molecular biology.

Statistical Genetic Modeling and Analysis of Complex Traits

S. Bull, C. Greenwood, J. Graham, 2014 .

S100A12 Serum Levels and PMN Counts Are Elevated in Childhood Systemic Vasculitides Especially Involving Proteinase 3 Specific Anti-neutrophil Cytoplasmic Antibodies

Kristen M. Gibson, C. Ross, D. Foell, 2018, Front. Pediatr..

Identification of Novel Adenosine Deaminase 2 Gene Variants and Varied Clinical Phenotype in Pediatric Vasculitis

Kristen M. Gibson, C. Ross, D. Foell, 2019, Arthritis & rheumatology.

Supplementary Materials for Chapter 8 : Small Sample Methods of The Handbook of Statistical Methods for Case-Control Studies

J. Graham, R. Platt, B. McNeney, 2018 .

Segregation and linkage analysis of a quantitative versus a qualitative trait in large pedigrees

E. Wijsman, E. Goode, K. Goddard, 1997, Genetic epidemiology.

Single-Nucleotide Polymorphisms in Reductase Genes Are not Associated with Response to Daunorubicin-Based Remission Induction

J. Graham, T. Grigliatti, J. Lubieniecka, 2013, Cancer Epidemiology, Biomarkers & Prevention.

Inference of gene-environment interaction from heterogeneous case-parent trios

J. Graham, B. McNeney, Pulindu Ratnasekera, 2022, bioRxiv.

Simple Measures of Individual Cluster-Membership Certainty for Hard Partitional Clustering

Jinko Graham, Dongmeng Liu, J. Graham, 2017, The American Statistician.

Secondary Analysis of Publicly Available Data Reveals Superoxide and Oxygen Radical Pathways are Enriched for Associations Between Type 2 Diabetes and Low‐Frequency Variants

Jinko Graham, J. Graham, M. Yazdanpanah, 2013, Annals of human genetics.

SimRVSequences: an R package to simulate genetic sequence data for pedigrees

Jinko Graham, Christina Nieuwoudt, Angela Brooks-Wilson, 2019, bioRxiv.

Simulating pedigrees ascertained for multiple disease-affected relatives

Jinko Graham, Christina Nieuwoudt, Samantha J. Jones, 2017, bioRxiv.

hapassoc: Software for Likelihood Inference of Trait Associations with SNP Haplotypes and Other Attributes

Jinko Graham, Brad McNeney, Kelly M. Burkett, 2006 .

elrm: Software Implementing Exact-Like Inference for Logistic Regression Models

Jinko Graham, Brad McNeney, David S. Zamar, 2007 .

LDheatmap: An R Function for Graphical Display of Pairwise Linkage Disequilibria Between Single Nucleotide Polymorphisms

Jinko Graham, Brad McNeney, Ji-Hyung Shin, 2006 .

Implementing Exact-like Inference for Logistic Regression Models

J. Graham, D. Zamar, B. McNeney, 2009 .

A discovery study of daunorubicin induced cardiotoxicity in a sample of acute myeloid leukemia patients prioritizes P450 oxidoreductase polymorphisms as a potential risk factor

J. Graham, T. Grigliatti, J. Lubieniecka, 2013, Front. Genet..

CrypticIBDcheck: an R package for checking cryptic relatedness in nominally unrelated individuals

Jinko Graham, Brad McNeney, Annick Nembot-Simo, 2013, Source Code for Biology and Medicine.

On the Use of Allelic Transmission Rates for Assessing Gene‐by‐Environment Interaction in Case‐Parent Trios

J. Graham, Ji-Hyung Shin, B. McNeney, 2010, Annals of human genetics.

Nonrandom occurrence of lymphoid cancer types in 140 families

J. Connors, G. Slack, A. Brooks-Wilson, 2017, Leukemia & lymphoma.

Cell culture-induced aberrant methylation of the imprinted IG DMR in human lymphoblastoid cell lines

C. Polychronakos, T. Pastinen, E. Grundberg, 2010, Epigenetics.

Genetic Variation in Cell Death Genes and Risk of Non-Hodgkin Lymphoma

R. Gascoyne, J. Connors, A. Brooks-Wilson, 2012, PloS one.

Disequilibrium likelihoods for fine-scale mapping of a rare allele.

E A Thompson, E. Thompson, J. Graham, 1998, American journal of human genetics.

Disequilibrium fine-mapping of a rare allele via coalescent models of gene ancestry

J. Graham, 1998 .

Different Disease Endotypes in Phenotypically Similar Vasculitides Affecting Small-to-Medium Sized Blood Vessels

Erin E. Gill, Kristen M. Gibson, C. Ross, 2021, Frontiers in Immunology.

Markov chain Monte Carlo sampling of gene genealogies conditional on unphased SNP genotype data

J. Graham, K. Burkett, B. McNeney, 2013, Statistical applications in genetics and molecular biology.

Controlling Correlational Bias via Confirmatory Factor Analysis of MTMM Data.

N. Collins, J. Graham, N L Collins, 1991, Multivariate behavioral research.

A data-smoothing approach to explore and test gene-environment interaction in case-parent trios

J. Graham, C. Infante-Rivard, Ji-Hyung Shin, 2014, Statistical applications in genetics and molecular biology.

The Contribution Plot: Decomposition and Graphical Display of the RV Coefficient, with Application to Genetic and Brain Imaging Biomarkers of Alzheimer’s Disease

M. Beg, Donghuan Lu, J. Graham, 2019, Human Heredity.

An exploration of linkage fine‐mapping on sequences from case‐control studies

Charith B. Karunarathna, J. Graham, P. Nickchi, 2021, bioRxiv.

Mendelian Randomization for Causal Inference of the Relationship between Obesity and 28-day Survival following Septic Shock

J. Graham, B. McNeney, 2017 .

A Note on Inference of Trait Associations with SNP Haplotypes and Other Attributes in Generalized Linear Models

Jinko Graham, Brad McNeney, Kelly Burkett, 2004, Human Heredity.

Association Between HLA–DPB1 and Antineutrophil Cytoplasmic Antibody–Associated Vasculitis in Children

C. Ross, D. Foell, J. Graham, 2023 .

Analysis of quantitative risk factors for a common oligogenic disease

E. Wijsman, G. Jarvik, J. Graham, 1995, Genetic epidemiology.

Age-dependent variation of genotypes in MHC II transactivator gene (CIITA) in controls and association to type 1 diabetes

M. Orho-Melander, E. Lindholm, L. Padyukov, 2012, Genes and Immunity.

Using Gene Genealogies to Detect Rare Variants Associated with Complex Traits

C. Greenwood, J. Graham, K. Burkett, 2014, Human Heredity.

Association Between HLA–DPB1 and Antineutrophil Cytoplasmic Antibody–Associated Vasculitis in Children

D. Foell, J. Graham, B. Drögemöller, 2022, Arthritis & rheumatology.

Formation of dendritic branching patterns

Jinko Graham, J. Graham, H. B. Uylings, 2003 .

LDheatmap: An R Function for Graphical Display of Pairwise Linkage Disequilibria Between Single Nucleotide Polymorphisms

Simon Fraser, Simon Fraser University, J. Graham, 2006 .

Phylogenetic Profiling and Stepwise Detection of Recombination Breakpoints in Hiv-1 Sequences from an Individual

J. Graham, F. Seillier-Moiseiwitsch, B. McNeney, 2022 .

Using gene genealogies to localize rare variants associated with complex traits in diploid populations

Charith B. Karunarathna, J. Graham, 2017, bioRxiv.

Secondary Analysis of Publicly Available Data Reveals Superoxide and Oxygen Radical Pathways are Enriched for Associations Between Type 2 Diabetes and Low‐Frequency Variants

J. Graham, M. Yazdanpanah, Chuhua Chen, 2013, Annals of human genetics.