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British Heart Foundation Grant
 
Job Vacancy for a Postdoctoral Statistical Geneticist/Bioinformatician
 
Grant awarded to carry out pilot study investigating the coagulation system in neonates with necrotizing enterocolitis
 
New Gene Variations Associated With Heart Rate Identified
 
The genetics of pro-arrhythmic adverse drug reactions.
We've just published a new review summarising the current state of knowledge on the genetics of drug induced pro-arrhythmia.
Faye wins poster prize for her Brugada screening study at the A to Z of Sudden Cardiac Death meeting in London.
Poster prize for Brugada Screening Study
Yalda gives a presentation on Genomics and Sudden Death at the Cardiac Arrhythmias: From Bench to Bedside (EP Curriculum day) 29th May 2015
Cardiac Arrhythmias: From Bench to Bedside (EP Curriculum day) 29th May 2015
Yalda presents the latest results from the CHARGE cardiac conduction exome-chip study at the European Society of Human Genetics, 6th June 2015
Low Frequency Putative Functional Variation in Cardiac Conduction - Oral presentation at ESHG, Glasgow June 6th 2015
Heather receives a Genetics Society Summer Studentship
Summer studentship awarded to Heather Jeffery to carry out functional follow up of novel loci associated with cardiac conduction using the zebrafish model.
MyologyForum
 
Yalda gives a presentation on recent work at the London Myology Forum
Yalda has been invited to give a talk on recent work which has identified a novel transcriptional regulator of cardiac and skeletal muscle development at this one day meeting to be held at the Royal Veterinary College, London - 22nd July 2015.
Yalda is invited to join the Editorial Board of the newly revamped Physiological Genomics Journal
 
Jay presents her work on transcription elongation at 44th European Muscle Conference, Warsaw, Poland
 
Presentation on the "Identification of a novel transcriptional regulator in skeletal and cardiac muscle" at the 10th Workshop for Cardiomyopathy and Contractility
The meeting will take place on the 27th November at the Wolfson Centre, Hammersmith Campus, Imperial College London.
MRC DTP PhD studentship available to study genetic determinants of heart rhythm
MRC DTP PhD studentship available - September 2016 start
Paper: Whole exome sequence analysis reveals a homozygous mutation in PNPLA2 as the cause of severe dilated cardiomyopathy secondary to neutral lipid storage disease
Paper accepted: "Whole exome sequence analysis reveals a homozygous mutation in PNPLA2 as the cause of severe dilated cardiomyopathy secondary to neutral lipid storage disease" in the International Journal of Cardiology
Jade
jade
New intern in the lab
We'd like to welcome Jade Crockford who joins us from Exeter University as an intern.
Genetic study identifies a new form of congenital muscular dystrophy
A new form of congenital muscular dystrophy has been discovered which is caused by mutations in a previously un-linked gene.
Newlife Logo
 
Newlife Logo
 
Newlife Logo
 
newlife
 
New Project Funding to investigate congenital forms of muscular dystrophy
Project funding received from the Newlife Charity to investigate molecular and therapeutic mechanisms of a novel form of congenital muscular dystrophy
ESHG 2017 Copenhagen Talk - Exome sequencing in Cardiomyopathy
Yalda is presenting results from a collaborative study to identify the underlying genetic cause of cardiomyopathy in two families.
ESHG2017
 
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