(Q27133763)

object named as

Christine E Seidman

0 references

Jong Bhak

object named as

Jong Bhak

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Kimberly Robasky

object named as

Kimberly Robasky

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author name string

Joseph V Thakuria

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Alexander Wait Zaranek

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Abraham M Rosenbaum

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Xiaodi Wu

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Misha Angrist

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Matthew J Callow

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Carlos Cano

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Michael F Chou

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Wendy K Chung

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Shawn M Douglas

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Preston W Estep

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Athurva Gore

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Peter Hulick

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Je-Hyuk Lee

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Byung Chul Kim

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Jong-Il Kim

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Zhe Li

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Michael F Murray

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Geoffrey B Nilsen

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Anugraha M Raman

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Hugh Y Rienhoff

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Matthew T Wheeler

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Ward Vandewege

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Daniel B Vorhaus

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Joyce L Yang

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John Aach

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Euan A Ashley

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Radoje Drmanac

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Seong-Jin Kim

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Jin Billy Li

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Leonid Peshkin

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Jeong-Sun Seo

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Kun Zhang

Proceedings of the National Academy of Sciences of the United States of America

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language of work or name

English

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publication date

24 July 2012

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published in

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volume

109

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issue

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page(s)

11920-7

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cites work

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From genetic privacy to open consent

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Familial hypertrophic cardiomyopathy mutations in the regulatory light chains of myosin affect their structure, Ca2+ binding, and phosphorylation

21 March 2017

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21 March 2017

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Genomics and privacy: implications of the new reality of closed data for the field

21 March 2017

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Using VAAST to identify an X-linked disorder resulting in lethality in male infants due to N-terminal acetyltransferase deficiency

21 March 2017

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Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays

21 March 2017

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Functional characterization of the antibiotic resistance reservoir in the human microflora

21 March 2017

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Targeted and genome-scale strategies reveal gene-body methylation signatures in human cells

21 March 2017

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Free Factories: Unified Infrastructure for Data Intensive Web Services

21 March 2017

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Integrating genotype and phenotype information: an overview of the PharmGKB project. Pharmacogenetics Research Network and Knowledge Base

21 March 2017

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Evolution and functional impact of rare coding variation from deep sequencing of human exomes

21 March 2017

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Personal omics profiling reveals dynamic molecular and medical phenotypes

7 April 2017

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A systematic survey of loss-of-function variants in human protein-coding genes

7 April 2017

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Keeping up with genetic discoveries in amyotrophic lateral sclerosis: the ALSoD and ALSGene databases

7 April 2017

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A probabilistic disease-gene finder for personal genomes.

28 September 2017

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Whole-genome sequencing in a patient with Charcot-Marie-Tooth neuropathy

28 September 2017

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A robust approach to identifying tissue-specific gene expression regulatory variants using personalized human induced pluripotent stem cells

28 September 2017

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Generation of functional human hepatic endoderm from human induced pluripotent stem cells

28 September 2017

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Digital RNA allelotyping reveals tissue-specific and allele-specific gene expression in human

28 September 2017

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Multiplex padlock targeted sequencing reveals human hypermutable CpG variations

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The incidentalome: a threat to genomic medicine

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31 May 2018

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A navigator for human genome epidemiology.

21 January 2018

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Crossref

https://api.crossref.org/works/10.1073%2FPNAS.1201904109

Familial Hypertrophic Cardiomyopathy-linked Alterations in Ca2+ Binding of Human Cardiac Myosin Regulatory Light Chain Affect Cardiac Muscle Contraction

21 January 2018

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Crossref

https://api.crossref.org/works/10.1073%2FPNAS.1201904109

One third of Danish hypertrophic cardiomyopathy patients with MYH7 mutations have mutations [corrected] in MYH7 rod region

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.1201904109

21 January 2018

Identifiers

DOI

10.1073/PNAS.1201904109

1 reference

ADS bibcode

2012PNAS..10911920B

0 references

1 reference

1 reference

PubMed publication ID

22797899

1 reference