Identifying the genetic causes of phenotypically diagnosed Pakistani mucopolysaccharidoses patients by whole genome sequencing

por Gul, Rutaba, Firasat, Sabika, Schubert, Mikkel, Ullah, Asmat, Peña, Elionora, Thuesen, Anne C. B., Hussain, Mulazim, Staeger, Frederik F., Gjesing, Anette P., Albrechtsen, Anders, Hansen, Torben
Publicado 2023

Identification of genetic variants associated with a wide spectrum of phenotypes clinically diagnosed as Sanfilippo and Morquio syndromes using whole genome sequencing

por Gul, Rutaba, Firasat, Sabika, Schubert, Mikkel, Ullah, Asmat, Peña, Elionora, Thuesen, Anne C. B., Gjesing, Annete P., Hussain, Mulazim, Tufail, Muhammad, Saqib, Muhammad, Afshan, Kiran, Hansen, Torben
Publicado 2023

Lactation Duration and Long-Term Thyroid Function: A Study among Women with Gestational Diabetes

por Panuganti, Pranati L., Hinkle, Stefanie N., Rawal, Shristi, Grunnet, Louise G., Lin, Yuan, Liu, Aiyi, Thuesen, Anne C. B., Ley, Sylvia H., Olesen, Sjurdur F., Zhang, Cuilin
Publicado 2018

Rationale and design of a prospective, clinical study of kidney biopsies in people with type 2 diabetes and severely increased albuminuria (the PRIMETIME 2 study)

por Møller, Marie, Borg, Rikke, Bressendorff, Iain, Fink, Lisbeth N, Gravesen, Eva, Jensen, Karina Haar, Hansen, Torben, Krustrup, Dorrit, Persson, Frederik, Rossing, Peter, Sembach, Frederikke E, Thuesen, Anne C B, Hansen, Ditte
Publicado 2023