Imperial College London

DrChristopherRhodes

Faculty of MedicineNational Heart & Lung Institute

Reader in Pulmonary Vascular Disease
 
 
 
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Contact

 

+44 (0)20 7594 7638c.rhodes07

 
 
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Location

 

535ICTEM buildingHammersmith Campus

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Summary

 

Publications

Citation

BibTex format

@article{Carss:2017:10.1016/j.ajhg.2016.12.003,
author = {Carss, KJ and Arno, G and Erwood, M and Stephens, J and Sanchis-Juan, A and Hull, S and Megy, K and Grozeva, D and Dewhurst, E and Malka, S and Plagnol, V and Penkett, C and Stirrups, K and Rizzo, R and Wright, G and Josifova, D and Bitner-Glindzicz, M and Scott, RH and Clement, E and Allen, L and Armstrong, R and Brady, AF and Carmichael, J and Chitre, M and Henderson, RHH and Hurst, J and MacLaren, RE and Murphy, E and Paterson, J and Rosser, E and Thompson, DA and Wakeling, E and Ouwehand, WH and Michaelides, M and Moore, AT and Webster, AR and Raymond, FL},
doi = {10.1016/j.ajhg.2016.12.003},
journal = {AMERICAN JOURNAL OF HUMAN GENETICS},
pages = {75--90},
title = {Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease},
url = {http://dx.doi.org/10.1016/j.ajhg.2016.12.003},
volume = {100},
year = {2017}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AU - Carss,KJ
AU - Arno,G
AU - Erwood,M
AU - Stephens,J
AU - Sanchis-Juan,A
AU - Hull,S
AU - Megy,K
AU - Grozeva,D
AU - Dewhurst,E
AU - Malka,S
AU - Plagnol,V
AU - Penkett,C
AU - Stirrups,K
AU - Rizzo,R
AU - Wright,G
AU - Josifova,D
AU - Bitner-Glindzicz,M
AU - Scott,RH
AU - Clement,E
AU - Allen,L
AU - Armstrong,R
AU - Brady,AF
AU - Carmichael,J
AU - Chitre,M
AU - Henderson,RHH
AU - Hurst,J
AU - MacLaren,RE
AU - Murphy,E
AU - Paterson,J
AU - Rosser,E
AU - Thompson,DA
AU - Wakeling,E
AU - Ouwehand,WH
AU - Michaelides,M
AU - Moore,AT
AU - Webster,AR
AU - Raymond,FL
DO - 10.1016/j.ajhg.2016.12.003
EP - 90
PY - 2017///
SN - 0002-9297
SP - 75
TI - Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease
T2 - AMERICAN JOURNAL OF HUMAN GENETICS
UR - http://dx.doi.org/10.1016/j.ajhg.2016.12.003
UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000391910500007&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=a2bf6146997ec60c407a63945d4e92bb
VL - 100
ER -