Cavelti-Weder, C; Muggli, B; Keller, C; Babians-Brunner, A; Biason-Lauber, A; Donath, M Y; Schmid-Grendelmeier, P (2012). Successful use of Omalizumab in a inadequately controlled type 2 diabetic Patient with severe Insulin Allergy. Diabetes Care, 35(6):41.
Hauri-Hohl, A; Meyer-Böni, M; Lang-Muritano, M; Hauri-Hohl, M; Schoenle, E J; Biason-Lauber, A (2011). Aromatase deficiency due to a functional variant in the placenta promoter and a novel missense mutation in the CYP19A1 gene. Clinical Endocrinology, 75(1):39-43.
Philibert, P; Biason-Lauber, A; Gueorguieva, I; Stuckens, C; Pienkowski, C; Lebon-Labich, B; Paris, F; Sultan, C (2011). Molecular analysis of WNT4 gene in four adolescent girls with mullerian duct abnormality and hyperandrogenism (atypical Mayer-Rokitansky-Küster-Hauser syndrome). Fertility and Sterility, 95(8):2683-2686.
Flück, C E; Meyer-Böni, M; Pandey, A V; Kempná, P; Miller, W L; Schoenle, E J; Biason-Lauber, A (2011). Why boys will be boys: two pathways of fetal testicular androgen biosynthesis are needed for male sexual differentiation. American Journal of Human Genetics, 89(2):201-218.
Rosa, S; Steigert, M; Lang-Muritano, M; l'Allemand, D; Schoenle, E J; Biason-Lauber, A (2010). Clinical, genetic and functional characteristics of three novel CYP17A1 mutations causing combined 17alpha-hydroxylase/17,20-lyase deficiency. Hormone Research in Paediatrics, 73(3):198-204.
Biason-Lauber, A (2010). Control of sex development. Best Practice & Research: Clinical Endocrinology & Metabolism, 24(2):163-86.
Biason-Lauber, A; Boscaro, M; Mantero, F; Balercia, G (2010). Defects of steroidogenesis. Journal of Endocrinological Investigation, 33(10):756-66.
Biason-Lauber, A; Konrad, D; Meyer, Monika; DeBeaufort, C; Schoenle, E J (2009). Ovaries and female phenotype in a girl with 46,XY karyotype and mutations in the CBX2 gene. American Journal of Human Genetics, 84(5):658-663.
Sultan, C; Biason-Lauber, A; Philibert, P (2009). Mayer-Rokitansky-Kuster-Hauser syndrome: recent clinical and genetic findings. Gynecological endocrinology, 25(1):8-11.
Philibert, P; Biason-Lauber, A; Rouzier, R; Pienkowski, C; Paris, F; Konrad, D; Schoenle, E; Sultan, C (2008). Identification and functional analysis of a new WNT4 gene mutation among 28 adolescent girls with primary amenorrhea and müllerian duct abnormalities: a French collaborative study. Journal of Clinical Endocrinology and Metabolism, 93(3):895-900.
Lavery, G G; Walker, E A; Tiganescu, A; Ride, J P; Shackleton, C H L; Tomlinson, J W; Connell, J M C; Ray, D W; Biason-Lauber, A; Malunowicz, E M; Arlt, W; Stewart, P M (2008). Steroid biomarkers and genetic studies reveal inactivating mutations in hexose-6-phosphate dehydrogenase in patients with cortisone reductase deficiency. Journal of Clinical Endocrinology and Metabolism, 93(10):3827-3832.
Biason-Lauber, A; Konrad, D (2008). WNT4 and sex development. Sexual Development, 2(4-5):210-218.