Searchable abstracts of presentations at key conferences in endocrinology

ea0050p181 | Clinical Biochemistry | SFEBES2017

Personalized medicine and endocrine disorders: the challenges of interpreting genetic variants

David Alessia , Ittisoponpisan SIrawit , Sternberg Michael JE

Introduction: Genetic projects, such as 100KGenomes, are identifying a vast amount of genetic variants that require interpretation. Several variants lack sufficient evidence to be classified as neutral or damaging. Such variants are annotated as ‘unclassified’ and interpretation of their biological effect is of paramount importance, but remains a major challenge. Variant predictors are widely used to prioritize variants for further studies...

ea0050p181 | Clinical Biochemistry | SFEBES2017

Personalized medicine and endocrine disorders: the challenges of interpreting genetic variants

David Alessia , Ittisoponpisan SIrawit , Sternberg Michael JE

Introduction: Genetic projects, such as 100KGenomes, are identifying a vast amount of genetic variants that require interpretation. Several variants lack sufficient evidence to be classified as neutral or damaging. Such variants are annotated as ‘unclassified’ and interpretation of their biological effect is of paramount importance, but remains a major challenge. Variant predictors are widely used to prioritize variants for further studies...

ea0044p27 | Adrenal and Steroids | SFEBES2016

Structural analysis of nicotinamide nucleotide transhydrogenase (NNT) genetic variants causing adrenal disorders

Metherell Lou , Guerra-Assuncao Jose Afonso , Sternberg Michael , David Alessia

Nicotinamide nucleotide transhydrogenase (NNT) is an integral protein of the inner mitochondrial membrane and plays a major role in maintaining the redox balance by catalysing the trans-hydrogenation between NADH and NADP+ and proton translocation across the mitochondrial membrane.Genetic variants in NNT have recently been reported in patients with familial glucocorticoid deficiency (FGD), combined mineralocorticoid and glucocorticoid deficiency...

ea0038oc1.2 | Early Career Oral Communications | SFEBES2015

Mutations in IGSF10 cause self-limited delayed puberty, via disturbance of GnRH neuronal migration

Howard Sasha , Guasti Leo , Ruiz-Babot Gerard , Mancini Alessandra , David Alessia , Storr Helen , Metherell Louise , Sternberg Michael , Cabrera Claudia , Warren Helen , Barnes Michael , Wehkalampi Karoliina , Andre Valentina , Gothilf Yoav , Cariboni Anna , Dunkel Leo

Background: Timing of puberty is associated with height, cardiovascular health and cancer risk, with a significant public health impact. Previous studies estimate that 60–80% of variation in the timing of pubertal onset is genetically determined. Self-limited delayed puberty (DP) segregates in an autosomal dominant pattern, but the underlying genetic background is unknown.Methods: We performed whole exome sequencing in 111 members of 18 families fro...