P. Shen

发表

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

R. W. Davis, L. Jin, P. Underhill, 1999, Proceedings of the National Academy of Sciences of the United States of America.

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

A. S. Torralba, J. Ross, P. Shen, 2003, Proceedings of the National Academy of Sciences of the United States of America.

A Test Case of Correlation Metric Construction of a Reaction Pathway from Measurements

J. Ross, A. Arkin, P. Shen, 1997 .

Conservation of the RB1 gene in human and primates

Peidong Shen, P. Shen, P. Oefner, 2005, Human mutation.

Phylogeography of Y-chromosome haplogroup I reveals distinct domains of prehistoric gene flow in europe.

Anne Cambon-Thomsen, Wolfgang Scheffrahn, Dragan Primorac, 2004, American journal of human genetics.

Rare variant detection using family-based sequencing analysis

Ronald W. Davis, P. Shen, C. Scharfe, 2013, Proceedings of the National Academy of Sciences.

High-quality DNA sequence capture of 524 disease candidate genes

Terence P. Speed, Gregory M. Enns, Curt Scharfe, 2011, Proceedings of the National Academy of Sciences.

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

Alice A. Lin, Colin Renfrew, Phillip Endicott, 2007, Proceedings of the National Academy of Sciences.

Multiplex target capture with double-stranded

P. Shen, C. Scharfe, Aung-Kyaw Chi, 2013 .

Multiplex target capture with double-stranded DNA probes

P. Shen, C. Scharfe, Aung-Kyaw Chi, 2013, Genome Medicine.

Steady-State Measurements on the Fructose 6-Phosphate/Fructose 1,6-Bisphosphate Interconversion Cycle

P. Shen, and Adam P. Arkin, D. Hauri, 1997 .

A two-pronged approach for rapid and high-throughput SARS-CoV-2 nucleic acid testing

P. Shen, A. Giraldez, C. Scharfe, 2020, medRxiv.

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

P. Shen, E. Fung, C. Scharfe, 2016, The Journal of molecular diagnostics : JMD.

Transplant Virus Detection Using Multiplex Targeted Sequencing.

P. Shen, E. Fung, C. Scharfe, 2018, The journal of applied laboratory medicine.

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

Hongyu Zhao, P. Shen, E. Fung, 2018, Genetics in Medicine.

Genetics and the History of the Samaritans: Y-Chromosomal Microsatellites and Genetic Affinity between Samaritans and Cohanim

M. Feldman, N. Rosenberg, P. Underhill, 2013, Human biology.

Origin, diffusion, and differentiation of Y-chromosome haplogroups E and J: inferences on the neolithization of Europe and later migratory events in the Mediterranean area.

P. Underhill, P. Shen, L. Cavalli-Sforza, 2004, American journal of human genetics.

Excavating Y-chromosome haplotype strata in Anatolia

P. Underhill, P. Shen, P. Oefner, 2003, Human Genetics.

Analysis of glycolysis metabolites by capillary zone electrophoresis with indirect UV detection.

P. Shen, P. Oefner, D. Hauri, 1996, Journal of capillary electrophoresis.

Global analysis of ATM polymorphism reveals significant functional constraint.

R. W. Davis, P. Shen, P. Oefner, 2001, American journal of human genetics.

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

Wenyi Wang, Terence P. Speed, Ronald W. Davis, 2010, Nucleic Acids Res..

The Role of Selection in the Evolution of Human Mitochondrial Genomes

Alfredo Coppa, Dennis P. Wall, David Modiano, 2006, Genetics.

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

Christopher R. Gignoux, S. Tishkoff, P. Underhill, 2008, Proceedings of the National Academy of Sciences.

A back migration from Asia to sub-Saharan Africa is supported by high-resolution analysis of human Y-chromosome haplotypes.

P. Underhill, P. Shen, L. Cavalli-Sforza, 2002, American journal of human genetics.

The phylogeography of Y chromosome binary haplotypes and the origins of modern human populations

L L Cavalli-Sforza, P. Underhill, P. Shen, 2001, Annals of human genetics.

Population genetic implications from sequence variation in four Y chromosome genes.

R. W. Davis, P. Underhill, P. Shen, 2000, Proceedings of the National Academy of Sciences of the United States of America.

Y-chromosome evidence of southern origin of the East Asian-specific haplogroup O3-M122.

Li Jin, Ranajit Chakraborty, Bing Su, 2005, American journal of human genetics.

Population genetic implications from DNA polymorphism in random human genomic sequences

P. Shen, P. Oefner, Wei-Hsien Yang, 2002, Human mutation.

Origins and divergence of the Roma (gypsies).

P. Underhill, P. Shen, P. Oefner, 2001, American journal of human genetics.

The Werner syndrome gene and global sequence variation.

P. Underhill, P. Shen, P. Oefner, 2001, Genomics.

Y chromosome sequence variation and the history of human populations

Li Jin, Jaume Bertranpetit, Alberto Piazza, 2000, Nature Genetics.

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

M W Feldman, R Thomson, M. Feldman, 2000, Proceedings of the National Academy of Sciences of the United States of America.

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

M. Feldman, D. Siegmund, P. Shen, 2002, Genetics.

Reconstruction of patrilineages and matrilineages of Samaritans and other Israeli populations from Y‐Chromosome and mitochondrial DNA sequence Variation

M. Feldman, P. Shen, P. Oefner, 2004, Human mutation.

Multiplex target capture with double-stranded DNA probes

P. Shen, C. Scharfe, Aung-Kyaw Chi, 2013, Genome Medicine.

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

Nader Pourmand, Curt Scharfe, Peidong Shen, 2010, Journal of biomedicine & biotechnology.

Conservation of the Class I -Tubulin Gene in Human Populations and Lack of Mutations in Lung Cancers and Paclitaxel-resistant Ovarian Cancers 1

P. Shen, P. Oefner, T. Fojo, 2002 .

A novel Y-chromosome variant puts an upper limit on the timing of first entry into the Americas.

P. Underhill, P. Shen, P. Oefner, 2003, American journal of human genetics.

Conservation of the class I beta-tubulin gene in human populations and lack of mutations in lung cancers and paclitaxel-resistant ovarian cancers.

P. Shen, P. Oefner, T. Fojo, 2002, Molecular cancer therapeutics.

Reduced genetic structure of the Iberian peninsula revealed by Y-chromosome analysis: implications for population demography

P. Underhill, P. Shen, P. Oefner, 2004, European Journal of Human Genetics.

Reduced Y-chromosome, but not mitochondrial DNA, diversity in human populations from West New Guinea.

P. Underhill, P. Shen, P. Oefner, 2003, American journal of human genetics.

Case-control study evaluating risk factors for SARS-CoV-2 outbreak amongst healthcare personnel at a tertiary care center

L. Steinmetz, P. Shen, W. Xiao, 2021, American Journal of Infection Control.

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

P. Shen, E. Ashley, E. Fung, 2015, Circulation research.

Y-Chromosome evidence for a northward migration of modern humans into Eastern Asia during the last Ice Age.

P. Underhill, P. Shen, L. Cavalli-Sforza, 1999, American journal of human genetics.

FEM1A is a candidate gene for polycystic ovary syndrome

P. Shen, P. Oefner, James G. Wilson, 2005, Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology.

Global sequence diversity of BRCA2: analysis of 71 breast cancer families and 95 control individuals of worldwide populations.

P. Underhill, P. Shen, P. Oefner, 1999, Human molecular genetics.

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

Christopher R. Gignoux, S. Tishkoff, P. Underhill, 2008, Proceedings of the National Academy of Sciences.

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

P. Shen, E. Fung, C. Scharfe, 2016, The Journal of molecular diagnostics : JMD.