1.
Inferring Identical-by-Descent Sharing of Sample Ancestors Promotes High-Resolution Relative Detection
by Ramstetter, Monica D
American journal of human genetics, 2018, Vol.103 (1), p.30-44
2.
Profiling and Leveraging Relatedness in a Precision Medicine Cohort of 92,455 Exomes
by Staples, Jeffrey
American journal of human genetics, 2018, Vol.102 (5), p.874-889
3.
PADRE: Pedigree-Aware Distant-Relationship Estimation
by Staples, Jeffrey
American journal of human genetics, 2016, Vol.99 (1), p.154-162
4.
Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS
by DeJesus-Hernandez, Mariely
Neuron (Cambridge, Mass.), 2011, Vol.72 (2), p.245-256
5.
A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD
by Renton, Alan E
Neuron (Cambridge, Mass.), 2011, Vol.72 (2), p.257-268
6.
Family-Based Association Tests for Genomewide Association Scans
by Chen, Wei-Min
American journal of human genetics, 2007, Vol.81 (5), p.913-926
7.
The Rare-Variant Generalized Disequilibrium Test for Association Analysis of Nuclear and Extended Pedigrees with Application to Alzheimer Disease WGS Data
by He, Zongxiao
American journal of human genetics, 2017, Vol.100 (2), p.193-204
8.
Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders
by Pinto, Dalila
American journal of human genetics, 2014, Vol.94 (5), p.677-694
9.
Finding the missing heritability of complex diseases
by Haines, Jonathan L
Nature (London), 2009, Vol.461 (7265), p.747-753
10.
Genome-wide Linkage Analysis of a Parkinsonian-Pyramidal Syndrome Pedigree by 500 K SNP Arrays
by Shojaee, Seyedmehdi
American journal of human genetics, 2008, Vol.82 (6), p.1375-1384
11.
Detection of Clinically Relevant Genetic Variants in Autism Spectrum Disorder by Whole-Genome Sequencing
by Jiang, Yong-hui
American journal of human genetics, 2013, Vol.93 (2), p.249-263
12.
Genotype imputation
by Li, Yun
Annual review of genomics and human genetics, 2009, Vol.10 (1), p.387-406
13.
Mutations in GANAB, Encoding the Glucosidase IIα Subunit, Cause Autosomal-Dominant Polycystic Kidney and Liver Disease
by Porath, Binu
American journal of human genetics, 2016, Vol.98 (6), p.1193-1207
14.
Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNA
by Turner, Tychele N
American journal of human genetics, 2016, Vol.98 (1), p.58-74
15.
The kinship2 R Package for Pedigree Data
by Sinnwell, Jason P
Human heredity, 2014, Vol.78 (2), p.91-93
16.
Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic Disease
by Karaca, Ender
Neuron (Cambridge, Mass.), 2015, Vol.88 (3), p.499-513
17.
18.
DISCO: Species Tree Inference using Multicopy Gene Family Tree Decomposition
by Willson, James
Systematic biology, Vol.71 (3), p.610-629
19.
Male sterility and fertility restoration in crops
by Chen, Letian
Annual review of plant biology, 2014, Vol.65 (1), p.579-606
20.
Handling Marker-Marker Linkage Disequilibrium: Pedigree Analysis with Clustered Markers
by Abecasis, Gonçalo R
American journal of human genetics, 2005, Vol.77 (5), p.754-767
