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Author Details
Full Name
Eric Scott
Affiliation
Rady Children's Institute for Genomic Medicine, University of California
ORCID
Career Start Year
2011
Papers
28
H Index
23
Expertise
CM4AI Collaborator
Trey Ideker (CM4AI)
PMID
Paper Title
Journal Title
Published Year
36400018
Evaluation of cell-free DNA approaches for multi-cancer early detection.
Cancer Cell
2022
30591557
Blacklisting variants common in private cohorts but not in public databases optimizes human exome analysis.
Proc Natl Acad Sci U S A
2019
31510681
Alignment-free filtering for cfNA fusion fragments.
Bioinformatics
2019
28626029
A homozygous founder mutation in <i>TRAPPC6B</i> associates with a neurodevelopmental disorder characterised by microcephaly, epilepsy and autistic features.
J Med Genet
2018
30013181
Biallelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 complex overactivity and disordered cortical neuronal migration.
Nat Genet
2018
28013290
Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stability.
Hum Mol Genet
2017
28092684
Biallelic mutations in the 3' exonuclease TOE1 cause pontocerebellar hypoplasia and uncover a role in snRNA processing.
Nat Genet
2017
26820543
The mutation significance cutoff: gene-level thresholds for variant predictions.
Nat Methods
2016
27588454
Autosomal-Recessive Mutations in the tRNA Splicing Endonuclease Subunit TSEN15 Cause Pontocerebellar Hypoplasia and Progressive Microcephaly.
Am J Hum Genet
2016
27428751
Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery.
Nat Genet
2016
27453578
Biallelic Mutations in Citron Kinase Link Mitotic Cytokinesis to Human Primary Microcephaly.
Am J Hum Genet
2016
27392077
Autosomal-Recessive Mutations in the tRNA Splicing Endonuclease Subunit TSEN15 Cause Pontocerebellar Hypoplasia and Progressive Microcephaly.
Am J Hum Genet
2016
27033521
Genome-wide screen identifies novel machineries required for both ciliogenesis and cell cycle arrest upon serum starvation.
Biochim Biophys Acta
2016
26026149
Functional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndrome.
Elife
2015
26483451
The human gene damage index as a gene-level approach to prioritizing exome variants.
Proc Natl Acad Sci U S A
2015
25848753
Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction.
Nat Genet
2015
26005868
Inactivating mutations in MFSD2A, required for omega-3 fatty acid transport in brain, cause a lethal microcephaly syndrome.
Nat Genet
2015
24482476
Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders.
Science
2014
25480035
Biallelic truncating mutations in FMN2, encoding the actin-regulatory protein Formin 2, cause nonsyndromic autosomal-recessive intellectual disability.
Am J Hum Genet
2014
24766810
CLP1 founder mutation links tRNA splicing and maturation to cerebellar development and neurodegeneration.
Cell
2014
24360807
Mutations in CSPP1 lead to classical Joubert syndrome.
Am J Hum Genet
2014
23453666
Whole-exome sequencing identifies mutated c12orf57 in recessive corpus callosum hypoplasia.
Am J Hum Genet
2013
23911318
AMPD2 regulates GTP synthesis and is mutated in a potentially treatable neurodegenerative brainstem disorder.
Cell
2013
23987214
Virmid: accurate detection of somatic mutations with sample impurity inference.
Genome Biol
2013
23386033
Phenotypic spectrum and prevalence of INPP5E mutations in Joubert syndrome and related disorders.
Eur J Hum Genet
2013
22729223
De novo somatic mutations in components of the PI3K-AKT3-mTOR pathway cause hemimegalencephaly.
Nat Genet
2012
22956686
Mutations in BCKD-kinase lead to a potentially treatable form of autism with epilepsy.
Science
2012
21685062
Error correction of high-throughput sequencing datasets with non-uniform coverage.
Bioinformatics
2011
1 - 28 of 28
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