Anne Simmonds

Genetic basis of inosine triphosphate pyrophosphohydrolase deficiency

Satoshi Sumi, Anthony M. Marinaki, Monica Arenas et al. · Human Genetics · 2002 · 267 citations

Genetic Disorder, Genetics, Biochemical Genetics +4

Alterations of uromodulin biology: a common denominator of the genetically heterogeneous FJHN/MCKD syndrome

Petr Vyleťal, Martina Kublová, Marie Hubálek Kalbáčová et al. · Kidney International · 2006 · 123 citations

Urology, Mendelian Disorder, Disease Mechanism +12

Pregnancy and infant loss: a survey of families’ experiences in Ontario Canada

Jo Watson, Anne Simmonds, Michelle La Fontaine et al. · BMC Pregnancy and Childbirth · 2019 · 57 citations · Full text

Adenylosuccinase deficiency: possibly underdiagnosed encephalopathy with variable clinical features

Martin Köhler, Birgit Assmann, Christa Bräutigam et al. · European Journal of Paediatric Neurology · 1999 · 49 citations

Ophthalmology, Neurological Disorder, Medicine +2

Nurses’ narratives of moral identity: Making a difference and reciprocal holding

Elizabeth Peter, Anne Simmonds, Joan Liaschenko · Nursing Ethics · 2016 · 39 citations