Experimental test of a method for determining causal connectivities of species in reactions

por Torralba, Antonio S., Yu, Kristine, Shen, Peidong, Oefner, Peter J., Ross, John
Publicado 2003

Recent common ancestry of human Y chromosomes: Evidence from DNA sequence data

por Thomson, Russell, Pritchard, Jonathan K., Shen, Peidong, Oefner, Peter J., Feldman, Marcus W.
Publicado 2000

Frequentist estimation of coalescence times from nucleotide sequence data using a tree-based partition.

por Tang, Hua, Siegmund, David O, Shen, Peidong, Oefner, Peter J, Feldman, Marcus W
Publicado 2002

Multiplex target capture with double-stranded DNA probes

por Shen, Peidong, Wang, Wenyi, Chi, Aung-Kyaw, Fan, Yu, Davis, Ronald W, Scharfe, Curt
Publicado 2013

A Novel Y-Chromosome Variant Puts an Upper Limit on the Timing of First Entry into the Americas

por Seielstad, Mark, Yuldasheva, Nadira, Singh, Nadia, Underhill, Peter, Oefner, Peter, Shen, Peidong, Wells, R. Spencer
Publicado 2003

Semi-Automated Library Preparation for High-Throughput DNA Sequencing Platforms

por Farias-Hesson, Eveline, Erikson, Jonathan, Atkins, Alexander, Shen, Peidong, Davis, Ronald W., Scharfe, Curt, Pourmand, Nader
Publicado 2010

Distribution of haplotypes from a chromosome 21 region distinguishes multiple prehistoric human migrations

por Jin, Li, Underhill, Peter A., Doctor, Vishal, Davis, Ronald W., Shen, Peidong, Cavalli-Sforza, L. Luca, Oefner, Peter J.
Publicado 1999

Reduced Y-Chromosome, but Not Mitochondrial DNA, Diversity in Human Populations from West New Guinea

por Kayser, Manfred, Brauer, Silke, Weiss, Gunter, Schiefenhövel, Wulf, Underhill, Peter, Shen, Peidong, Oefner, Peter, Tommaseo-Ponzetta, Mila, Stoneking, Mark
Publicado 2003

Global Analysis of ATM Polymorphism Reveals Significant Functional Constraint

por Thorstenson, Yvonne R., Shen, Peidong, Tusher, Virginia G., Wayne, Tierney L., Davis, Ronald W., Chu, Gilbert, Oefner, Peter J.
Publicado 2001

Rare variant detection using family-based sequencing analysis

por Peng, Gang, Fan, Yu, Palculict, Timothy B., Shen, Peidong, Ruteshouser, E. Cristy, Chi, Aung-Kyaw, Davis, Ronald W., Huff, Vicki, Scharfe, Curt, Wang, Wenyi
Publicado 2013

Transplant Virus Detection Using Multiplex Targeted Sequencing

por Tan, Susanna K., Shen, Peidong, Lefterova, Martina I., Sahoo, Malaya K., Fung, Eula, Odegaard, Justin I., Davis, Ronald W., Pinsky, Benjamin A., Scharfe, Curt
Publicado en J Appl Lab Med (2018)

Revealing the prehistoric settlement of Australia by Y chromosome and mtDNA analysis

por Hudjashov, Georgi, Kivisild, Toomas, Underhill, Peter A., Endicott, Phillip, Sanchez, Juan J., Lin, Alice A., Shen, Peidong, Oefner, Peter, Renfrew, Colin, Villems, Richard, Forster, Peter
Publicado 2007

High-quality DNA sequence capture of 524 disease candidate genes

por Shen, Peidong, Wang, Wenyi, Krishnakumar, Sujatha, Palm, Curtis, Chi, Aung-Kyaw, Enns, Gregory M., Davis, Ronald W., Speed, Terence P., Mindrinos, Michael N., Scharfe, Curt
Publicado 2011

Next-Generation Molecular Testing of Newborn Dried Blood Spots for Cystic Fibrosis

por Lefterova, Martina I., Shen, Peidong, Odegaard, Justin I., Fung, Eula, Chiang, Tsoyu, Peng, Gang, Davis, Ronald W., Wang, Wenyi, Kharrazi, Martin, Schrijver, Iris, Scharfe, Curt
Publicado en J Mol Diagn (2016)

Y-chromosomal evidence of a pastoralist migration through Tanzania to southern Africa

por Henn, Brenna M., Gignoux, Christopher, Lin, Alice A., Oefner, Peter J., Shen, Peidong, Scozzari, Rosaria, Cruciani, Fulvio, Tishkoff, Sarah A., Mountain, Joanna L., Underhill, Peter A.
Publicado 2008

Combining newborn metabolic and DNA analysis for second-tier testing of methylmalonic acidemia

por Peng, Gang, Shen, Peidong, Gandotra, Neeru, Le, Anthony, Fung, Eula, Jelliffe-Pawlowski, Laura, Davis, Ronald W., Enns, Gregory M., Zhao, Hongyu, Cowan, Tina M., Scharfe, Curt
Publicado en Genet Med (2018)

Identification of rare DNA variants in mitochondrial disorders with improved array-based sequencing

por Wang, Wenyi, Shen, Peidong, Thiyagarajan, Sreedevi, Lin, Shengrong, Palm, Curtis, Horvath, Rita, Klopstock, Thomas, Cutler, David, Pique, Lynn, Schrijver, Iris, Davis, Ronald W., Mindrinos, Michael, Speed, Terence P., Scharfe, Curt
Publicado 2011

A Rapid, High-Quality, Cost-Effective, Comprehensive and Expandable Targeted Next-Generation Sequencing Assay for Inherited Heart Diseases

por Wilson, Kitchener D., Shen, Peidong, Fung, Eula, Karakikes, Ioannis, Zhang, Angela, InanlooRahatloo, Kolsoum, Odegaard, Justin, Sallam, Karim, Davis, Ronald W., Lui, George K., Ashley, Euan A., Scharfe, Curt, Wu, Joseph C.
Publicado en Circ Res (2015)

Population genetic implications from sequence variation in four Y chromosome genes

por Shen, Peidong, Wang, Frank, Underhill, Peter A., Franco, Claudia, Yang, Wei-Hsien, Roxas, Adriane, Sung, Raphael, Lin, Alice A., Hyman, Richard W., Vollrath, Douglas, Davis, Ronald W., Cavalli-Sforza, L. Luca, Oefner, Peter J.
Publicado 2000

A Back Migration from Asia to Sub-Saharan Africa Is Supported by High-Resolution Analysis of Human Y-Chromosome Haplotypes

por Cruciani, Fulvio, Santolamazza, Piero, Shen, Peidong, Macaulay, Vincent, Moral, Pedro, Olckers, Antonel, Modiano, David, Holmes, Susan, Destro-Bisol, Giovanni, Coia, Valentina, Wallace, Douglas C., Oefner, Peter J., Torroni, Antonio, Cavalli-Sforza, L. Luca, Scozzari, Rosaria, Underhill, Peter A.
Publicado 2002