Follow
Mark Curran
Mark Curran
Janssen R&D LLC
Verified email at its.jnj.com
Title
Cited by
Cited by
Year
A mechanistic link between an inherited and an acquird cardiac arrthytmia: HERG encodes the IKr potassium channel
MC Sanguinetti, C Jiang, ME Curran, MT Keating
Cell 81 (2), 299-307, 1995
28651995
A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome
ME Curran, I Splawski, KW Timothy, GM Vincen, ED Green, MT Keating
Cell 80 (5), 795-803, 1995
27711995
Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
Q Wang, ME Curran, I Splawski, TC Burn, JM Millholland, TJ VanRaay, ...
Nature genetics 12 (1), 17-23, 1996
22051996
Coassembly of KVLQT1 and minK (IsK) proteins to form cardiac IKS potassium channel
MC Sanguinetti, ME Curran, A Zou, J Shen, PS Specter, DL Atkinson, ...
Nature 384 (6604), 80-83, 1996
21391996
Spectrum of HERG K+-channel dysfunction in an inherited cardiac arrhythmia.
MC Sanguinetti, ME Curran, PS Spector, MT Keating
Proceedings of the National Academy of Sciences 93 (5), 2208-2212, 1996
5781996
The elastin gene is disrupted by a translocation associated with supravalvular aortic stenosis
ME Curran, DL Atkinson, AK Ewart, CA Morris, MF Leppert, MT Keating
Cell 73 (1), 159-168, 1993
5271993
Fast inactivation causes rectification of the IKr channel.
PS Spector, ME Curran, A Zou, MT Keating, MC Sanguinetti
The Journal of general physiology 107 (5), 611-619, 1996
5231996
A genomewide analysis provides evidence for novel linkages in inflammatory bowel disease in a large European cohort
J Hampe, S Schreiber, SH Shaw, KF Lau, S Bridger, AJS Macpherson, ...
The American journal of human genetics 64 (3), 808-816, 1999
4451999
Idiopathic congenital central hypoventilation syndrome: analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in …
DE Weese‐Mayer, EM Berry‐Kravis, L Zhou, BS Maher, JM Silvestri, ...
American journal of medical genetics Part A 123 (3), 267-278, 2003
4322003
Class III Antiarrhythmic Drugs Block HERG, a Human Cardiac Delayed Rectifier K+ Channel: Open-Channel Block by Methanesulfonanilides
PS Spector, ME Curran, MT Keating, MC Sanguinetti
Circulation research 78 (3), 499-503, 1996
3701996
Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: implications for arrhythmogenic susceptibility and Brugada/long …
MJ Ackerman, I Splawski, JC Makielski, DJ Tester, ML Will, KW Timothy, ...
Heart rhythm 1 (5), 600-607, 2004
3282004
Ethnic differences in cardiac potassium channel variants: implications for genetic susceptibility to sudden cardiac death and genetic testing for congenital long QT syndrome
MJ Ackerman, DJ Tester, GS Jones, ML Will, CR Burrow, ME Curran
Mayo clinic proceedings 78 (12), 1479-1487, 2003
3272003
Linkage of inflammatory bowel disease to human chromosome 6p
J Hampe, SH Shaw, R Saiz, N Leysens, A Lantermann, S Mascheretti, ...
The American Journal of Human Genetics 65 (6), 1647-1655, 1999
2891999
Genome screen for QTLs contributing to normal variation in bone mineral density and osteoporosis
DL Koller, MJ Econs, PA Morin, JC Christian, SL Hui, P Parry, ME Curran, ...
The Journal of Clinical Endocrinology & Metabolism 85 (9), 3116-3120, 2000
2452000
A functional genomics predictive network model identifies regulators of inflammatory bowel disease
LA Peters, J Perrigoue, A Mortha, A Iuga, W Song, EM Neiman, ...
Nature genetics 49 (10), 1437-1449, 2017
2312017
Genetic analysis of inflammatory bowel disease in a large European cohort supports linkage to chromosomes 12 and 16
ME Curran, KF Lau, J Hampe, S Schreiber, S Bridger, AJS Macpherson, ...
Gastroenterology 115 (5), 1066-1071, 1998
2221998
Linkage of a QTL contributing to normal variation in bone mineral density to chromosome 11q12–13
DL Koller, LA Rodriguez, JC Christian, CW Slemenda, MJ Econs, SL Hui, ...
Journal of Bone and Mineral Research 13 (12), 1903-1908, 1998
1901998
Sudden infant death syndrome: association with a promoter polymorphism of the serotonin transporter gene
DE Weese‐Mayer, EM Berry‐Kravis, BS Maher, JM Silvestri, ME Curran, ...
American Journal of Medical Genetics Part A 117 (3), 268-274, 2003
1662003
Evidence for a NOD2-independent susceptibility locus for inflammatory bowel disease on chromosome 16p
J Hampe, H Frenzel, MM Mirza, PJP Croucher, A Cuthbert, S Mascheretti, ...
Proceedings of the National Academy of Sciences 99 (1), 321-326, 2002
1422002
Sudden infant death syndrome: case-control frequency differences at genes pertinent to early autonomic nervous system embryologic development
DE Weese-Mayer, EM Berry-Kravis, L Zhou, BS Maher, ME Curran, ...
Pediatric research 56 (3), 391-395, 2004
1312004
The system can't perform the operation now. Try again later.
Articles 1–20