Author details

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Full Name

Emily L Crawford

Affiliation

ORCID

Career Start Year

2006

Papers

15

H Index

12

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36439700	Ephrin-B2-expressing natural killer cells induce angiogenesis.	JVS-Vascular Science	2022
29499131	Dynamic Regulation of Long-Chain Fatty Acid Oxidation by a Noncanonical Interaction between the MCL-1 BH3 Helix and VLCAD.	Molecular Cell	2018
25270638	Consensus Genotyper for Exome Sequencing (CGES): improving the quality of exome variant genotypes.	Bioinformatics	2015
24695082	Pro32Pro33 mutations in the integrin Î²3 PSI domain result in Î±IIbÎ²3 priming and enhanced adhesion: reversal of the hypercoagulability phenotype by the Src inhibitor SKI-606.	Mol Pharmacol	2014
25363760	Synaptic, transcriptional and chromatin genes disrupted in autism.	Nature	2014
24768552	Convergence of genes and cellular pathways dysregulated in autism spectrum disorders.	Am J Hum Genet	2014
22566635	A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism.	Proc Natl Acad Sci U S A	2012
22843504	Individual common variants exert weak effects on the risk for autism spectrum disorders.	Hum Mol Genet	2012
22495311	Patterns and rates of exonic de novo mutations in autism spectrum disorders.	Nature	2012
21658581	Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.	Neuron	2011
20663923	A genome-wide scan for common alleles affecting risk for autism.	Hum Mol Genet	2010
20531469	Functional impact of global rare copy number variation in autism spectrum disorders.	Nature	2010
19404257	Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.	Nature	2009
17457615	Complex chromosome 17p rearrangements associated with low-copy repeats in two patients with congenital anomalies.	Hum Genet	2007
16507369	Isolating apparently pure libraries of replication origins from complex genomes.	Mol Cell	2006

1 - 15 of 15

James S Sutcliffe

Vanderbilt Genetics Institute, Vanderbilt University

Co-authored papers 11

Co-authored papers 10

Joseph D Buxbaum

Icahn School of Medicine at Mount Sinai

Co-authored papers 8

Co-authored papers 8

Gerard D Schellenberg

Co-authored papers 7

Co-authored papers 7

Alexander Kolevzon

Co-authored papers 6

Bridget A Fernandez

Memorial University of Newfoundland

Co-authored papers 6

Geraldine Dawson

Co-authored papers 6

Stephen W Scherer

The Hospital for Sick Children

Co-authored papers 6

Co-authored papers 6

Co-authored papers 6

Daniel H Geschwind

University of California los angeles

Co-authored papers 6

Hospital for Sick Children, University of Toronto

Co-authored papers 6

Catalina Betancur

Co-authored papers 6

Patrick F Bolton

Co-authored papers 5

Louise Gallagher

Co-authored papers 5

Hakon Hakonarson

The Center for Applied Genomics, Children's Hospital of Philadelphia

Co-authored papers 5

John I Nurnberger

Stark Neurosciences Research Institute, Indiana University School of Medicine

Co-authored papers 5

Co-authored papers 5

Stephen J Guter

Co-authored papers 5

University of California los angeles

Co-authored papers 5

Co-authored papers 5

Christine M Freitag

Co-authored papers 5

Eftichia Duketis

Co-authored papers 5

Sabine M Klauck

Co-authored papers 5

Oxford Brookes University

Co-authored papers 4

Margaret A Pericak-Vance

Co-authored papers 4

Agatino Battaglia

Co-authored papers 4

INSERM U

Co-authored papers 4

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