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Chiao‐Feng Lin

Directorate-General for Interpretation · TW
Area of research
Genetics · Physiology
Research interest
Research interests include Genomics and Rare Diseases, Alzheimer's disease research and treatments, Genetic Associations and Epidemiology, and RNA and protein synthesis mechanisms.
h-index
28
citations
17,974
works
59
NIH funding
primary concept
email

Recent publications

A Rigorous Interlaboratory Examination of the Need to Confirm Next-Generation Sequencing–Detected Variants with an Orthogonal Method in Clinical Genetic Testing
Journal of Molecular Diagnostics 2019cited by 78position: middledoi
Assessing predictions of the impact of variants on splicing in CAGI5
Human Mutation 2019cited by 26position: middledoi
Global and local ancestry in African‐Americans: Implications for Alzheimer's disease risk
Alzheimer s & Dementia 2015cited by 55position: middledoi
Association of Long Runs of Homozygosity With Alzheimer Disease Among African American Individuals
JAMA Neurology 2015cited by 51position: middledoi
Synaptic, transcriptional and chromatin genes disrupted in autism
Nature 2014cited by 2,909position: middledoi
Gene-Wide Analysis Detects Two New Susceptibility Genes for Alzheimer's Disease
PLoS ONE 2014cited by 1,405position: middledoi
Convergent genetic and expression data implicate immunity in Alzheimer's disease
Alzheimer s & Dementia 2014cited by 207position: middledoi
Rarity of the Alzheimer Disease–Protective<i>APP</i>A673T Variant in the United States
JAMA Neurology 2014cited by 49position: middledoi
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
Nature Genetics 2013cited by 4,640position: middledoi
Variants in the ATP-Binding Cassette Transporter (ABCA7), Apolipoprotein E ϵ4, and the Risk of Late-Onset Alzheimer Disease in African Americans
JAMA 2013cited by 457position: middledoi
Rare Complete Knockouts in Humans: Population Distribution and Significant Role in Autism Spectrum Disorders
Neuron 2013cited by 279position: middledoi
Patterns and rates of exonic de novo mutations in autism spectrum disorders
Nature 2012cited by 1,795position: middledoi

Grants

No grants ingested yet.

Frequent collaborators

Liran Carmel · Hebrew University of Jerusalem1 papers (2019–2019) · 1 papers (2019–2019) · 1 papers (2019–2019)Muhammed Hasan Çelik · Technical University of Munich1 papers (2019–2019)Valer Gotea · National Human Genome Research Institute1 papers (2019–2019)Noa Cohen · Hebrew University of Jerusalem1 papers (2019–2019)Stephen M. Mount · University of Maryland, College Park1 papers (2019–2019)William G. Fairbrother · Brown University1 papers (2019–2019) · 1 papers (2019–2019)Robert L. Nussbaum · Mayo Clinic in Florida1 papers (2019–2019)Rebecca Truty · Invitae (United States)1 papers (2019–2019)Stephen E. Lincoln · Case Western Reserve University1 papers (2019–2019)Thi Yen Duong Nguyen · Technical University of Munich1 papers (2019–2019) · 1 papers (2019–2019)Ron Unger · University of Kentucky1 papers (2019–2019)Žiga Avsec · Google (United States)1 papers (2019–2019)Justin M. Zook · Directorate-General for Interpretation1 papers (2019–2019) · 1 papers (2019–2019) · 1 papers (2019–2019)Jun Cheng · Google DeepMind (United Kingdom)1 papers (2019–2019)