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Publications

Natural history and cell-of-origin of TCF3-ZNF384 and PTPN11 mutations in monozygotic twins with concordant BCP-ALL.

Bueno C. et al, (2019), Blood

Genetic Risk Score for Coronary Disease Identifies Predispositions to Cardiovascular and Noncardiovascular Diseases

Ntalla I. et al, (2019), Journal of the American College of Cardiology, 73, 2932 - 2942

Identification of infants with increased type 1 diabetes genetic risk for enrollment into Primary Prevention Trials-GPPAD-02 study design and first results.

Winkler C. et al, (2019), Pediatr Diabetes

Do health professionals value genomic testing? A discrete choice experiment in inherited cardiovascular disease.

Buchanan J. et al, (2019), Eur J Hum Genet

Impairment of Nrf2- and Nitrergic-Mediated Gastrointestinal Motility in an MPTP Mouse Model of Parkinson's Disease.

Sampath C. et al, (2019), Dig Dis Sci

Common Genetic Variations Associated with the Persistence of Immunity following Childhood Immunization.

O'Connor D. et al, (2019), Cell Rep, 27, 3241 - 3253.e4

A single-dose ChAdOx1-vectored vaccine provides complete protection against Nipah Bangladesh and Malaysia in Syrian golden hamsters.

van Doremalen N. et al, (2019), PLoS Negl Trop Dis, 13

Genetically modulated educational attainment and coronary disease risk.

Zeng L. et al, (2019), Eur Heart J

A knottin scaffold directs the CXC-chemokine-binding specificity of tick evasins.

Lee AW. et al, (2019), J Biol Chem

The impact of blood pressure variability on coronary arterial lumen dimensions as assessed by optical coherence tomography in patients with ST-elevation myocardial infarction.

Soud M. et al, (2019), Cardiovasc Revasc Med

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.

Turcot V. et al, (2019), Nat Genet

Remission of inflammatory bowel disease in Glucose-6-Phosphatase 3 deficiency by allogeneic haematopoietic stem cell transplantation.

Bolton C. et al, (2019), J Crohns Colitis

Author Correction: A dynamic three-step mechanism drives the HIV-1 pre-fusion reaction.

Iliopoulou M. et al, (2019), Nat Struct Mol Biol, 26

Evolutionary history of human colitis-associated colorectal cancer

Baker A-M. et al, (2019), Gut, 68, 985 - 995

A catalog of genetic loci associated with kidney function from analyses of a million individuals.

Wuttke M. et al, (2019), Nat Genet, 51, 957 - 972

Genetic and functional data identifying Cd101 as a type 1 diabetes (T1D) susceptibility gene in nonobese diabetic (NOD) mice.

Mattner J. et al, (2019), PLoS Genet, 15

Author Correction: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries.

Shrine N. et al, (2019), Nat Genet, 51

Pioneering function of Isl1 in the epigenetic control of cardiomyocyte cell fate.

Gao R. et al, (2019), Cell Res, 29, 486 - 501

Disruption of FOXF2 as a Likely Cause of Absent Uvula in an Egyptian Family.

Seselgyte R. et al, (2019), J Dent Res, 98, 659 - 665

Delineation of dominant and recessive forms of LZTR1-associated Noonan syndrome.

Pagnamenta AT. et al, (2019), Clin Genet, 95, 693 - 703

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