FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Susan Moore

Research Profile

Disorders

Chemicals & Drugs

Geographic Areas

Newfoundland and Labrador

Physiology

Living Beings

Infants

Concepts & Ideas

Prevalence

Co-author Network

Publications

TOP 3
Krista Mahoney; Muhammed Alam; David Buckley; Patrick Parfrey; Sharon Penney; TL Young; Susan J Moore
High incidence of pediatric idiopathic epilepsy is associated with familial and autosomal dominant disease in Eastern Newfoundland.
Krista Mahoney; Susan J Moore; David Buckley; Muhammed Alam; Patrick Parfrey; Sharon Penney; Nancy Merner; Kathy Hodgkinson; Terry-Lynn Young
Variable neurologic phenotype in a GEFS+ family with a novel mutation in SCN1A.
Adelene D Rasalam; Hazel Hailey; J H G Williams; Susan J Moore; Peter D Turnpenny; DJ Lloyd; John C S Dean
Characteristics of fetal anticonvulsant syndrome associated autistic disorder.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Susan Moore (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2012: Krista Mahoney; Muhammed Alam; David Buckley; Patrick Parfrey; Sharon Penney; TL Young; Susan J Moore
High incidence of pediatric idiopathic epilepsy is associated with familial and autosomal dominant disease in Eastern Newfoundland.
Epilepsy research 2012;98(2-3):140-7.
2009: Krista Mahoney; Susan J Moore; David Buckley; Muhammed Alam; Patrick Parfrey; Sharon Penney; Nancy Merner; Kathy Hodgkinson; Terry-Lynn Young
Variable neurologic phenotype in a GEFS+ family with a novel mutation in SCN1A.
Seizure : the journal of the British Epilepsy Association 2009;18(7):492-7.
2005: Adelene D Rasalam; Hazel Hailey; J H G Williams; Susan J Moore; Peter D Turnpenny; DJ Lloyd; John C S Dean
Characteristics of fetal anticonvulsant syndrome associated autistic disorder.
Developmental medicine and child neurology 2005;47(8):551-5.
2005: Susan J Moore; Jane S Green; Yanli Fan; Ashvinder K Bhogal; Elizabeth Dicks; Bridget A Fernandez; Mark Stefanelli; Christopher Murphy; Benvon C Cramer; John C S Dean; Philip L Beales; Nicholas Katsanis; Anne S Bassett; William S Davidson; Patrick S Parfrey
Clinical and genetic epidemiology of Bardet-Biedl syndrome in Newfoundland: a 22-year prospective, population-based, cohort study.
American journal of medical genetics. Part A 2005;132(4):352-60.
2004: Yanli Fan; Muneer A Esmail; Stephen J Ansley; Oliver E Blacque; Keith A Boroevich; Alison J Ross; Susan J Moore; Jose L Badano; Helen May-Simera; Deanna S Compton; Jane S Green; Richard Alan Lewis; Mieke M van Haelst; Patrick S Parfrey; David Baillie; Philip L Beales; Nicholas Katsanis; William S Davidson; Michel R Leroux
Mutations in a member of the Ras superfamily of small GTP-binding proteins causes Bardet-Biedl syndrome.
Nature genetics 2004;36(9):989-93.
2004: Yanli Fan; Proton Rahman; Lynette Peddle; Donna Hefferton; N Gladney; Susan J Moore; Jane S Green; Patrick S Parfrey; William S Davidson
Bardet-Biedl syndrome 1 genotype and obesity in the Newfoundland population.
International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity 2004;28(5):680-4.
2002: Simon J Glover; Anthony G Quinn; Philippa Barter; Jane Hart; Susan J Moore; John C S Dean; Peter D Turnpenny
Ophthalmic findings in fetal anticonvulsant syndrome(s).
Ophthalmology 2002;109(5):942-7.
2002: John C S Dean; Hazel Hailey; Susan J Moore; DJ Lloyd; Peter D Turnpenny; Julian Little
Long term health and neurodevelopment in children exposed to antiepileptic drugs before birth.
Journal of medical genetics 2002;39(4):251-9.
2000: Susan J Moore; Peter D Turnpenny; A Quinn; S Glover; DJ Lloyd; T Montgomery; John C S Dean
A clinical study of 57 children with fetal anticonvulsant syndromes.
Journal of medical genetics 2000;37(7):489-97.
2000: John C S Dean; Susan J Moore; Peter D Turnpenny
Developing diagnostic criteria for the fetal anticonvulsant syndromes.
Seizure : the journal of the British Epilepsy Association 2000;9(3):233-4.
1999: John C S Dean; Susan J Moore; A Osborne; J Howe; Peter D Turnpenny
Fetal anticonvulsant syndrome and mutation in the maternal MTHFR gene.
Clinical genetics 1999;56(3):216-20.
1999: Susan J Moore; L Strain; G F Cole; Z Miedzybrodzka; K F Kelly; John C S Dean
Fragile X syndrome with FMR1 and FMR2 deletion.
Journal of medical genetics 1999;36(7):565-6.
1999: Susan J Moore; I A Auchterlonie; G F Cole; E S Gray; John C S Dean
Partial lipodystrophy presenting with myopathy.
Developmental medicine and child neurology 1999;41(2):127-31.
1998: Susan J Moore; N E Haites; Iain Broom; I White; R J Coleman; Morteza Pourfarzam; Andrew A M Morris
Acylcarnitine analysis in the investigation of myopathy.
Journal of inherited metabolic disease 1998;21(4):427-8.