Author details

Full Name

Chiao-Feng Lin

Affiliation

ORCID

Career Start Year

2004

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
35041930	Automated Pharmacogenomic Reports for Clinical Genome Sequencing.	J Mol Diagn	2022
34417613	Corrigendum to: Detecting Genetic Ancestry and Adaptation in the Taiwanese Han People.	Molecular Biology and Evolution	2021
32439067	Bioinformatics in Clinical Genomic Sequencing.	Clin Lab Med	2020
31301154	Assessing predictions of the impact of variants on splicing in CAGI5.	Hum Mutat	2019
30610921	A Rigorous Interlaboratory Examination of the Need to Confirm Next-Generation Sequencing-Detected Variants with an Orthogonal MethodÂ in Clinical Genetic Testing.	J Mol Diagn	2019
26092349	Global and local ancestry in African-Americans: Implications for Alzheimer's disease risk.	Alzheimers Dement	2016
26927186	Bioinformatics Workflow for Clinical Whole Genome Sequencing at Partners HealthCare Personalized Medicine.	J Pers Med	2016
26366463	Association of Long Runs of Homozygosity With Alzheimer Disease Among African American Individuals.	JAMA Neurol	2015
25531812	Rarity of the Alzheimer disease-protective APP A673T variant in the United States.	JAMA Neurol	2015
25480377	HIPPIE: a high-throughput identification pipeline for promoter interacting enhancer elements.		2015
24922517	Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease.	PLoS One	2014
25363760	Synaptic, transcriptional and chromatin genes disrupted in autism.	Nature	2014
25199842	Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study.	JAMA Neurol	2014
24510649	Analyzing copy number variation using SNP array data: protocols for calling CNV and association tests.	Current Protocols in Human Genetics	2013
24162737	Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease.	Nat Genet	2013
23943636	DRAW+SneakPeek: analysis workflow and quality metric management for DNA-seq experiments.		2013
23352160	Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders.	Neuron	2013
23571587	Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E Ïµ4,and the risk of late-onset Alzheimer disease in African Americans.	JAMA	2013
22495311	Patterns and rates of exonic de novo mutations in autism spectrum disorders.	Nature	2012
22393306	U12-type spliceosomal introns of Insecta.	International Journal of Biological Sciences	2012
20163699	Evolutionary dynamics of U12-type spliceosomal introns.	BMC Evol Biol	2010
17095541	Spliceosomal small nuclear RNA genes in 11 insect genomes.	RNA	2007
17994087	Evolution of genes and genomes on the Drosophila phylogeny.	Nature	2007
17939861	Birth and death of gene overlaps in vertebrates.	BMC Evolutionary Biology	2007
16387879	Molecular evolution in the Drosophila melanogaster species subgroup: frequent parameter fluctuations on the timescale of molecular divergence.	Genetics	2006
15680581	Overlapping genes in vertebrate genomes.	Computational Biology and Chemistry	2005
15100401	Determinants of plant U12-dependent intron splicing efficiency.	Plant Cell	2004