Roeleveld, Nel

Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity

Thorleifsson, G., Walters, G. B., Gudbjartsson, D. F., Steinthorsdottir, V., Sulem, P., Helgadottir, A., Styrkarsdottir, U., Gretarsdottir, S., Thorlacius, S., Jonsdottir, I., et al. (2009) · Nature Genetics

Genetic Associations and EpidemiologyGenetic Mapping and Diversity in Plants and Animals

Cited by 1,375

Impact of maternal body mass index and gestational weight gain on pregnancy complications: an individual participant data meta‐analysis of European, North American and Australian cohorts

Santos, S., Voerman, E., Amiano, P., Barros, H., Beilin, L., Bergström, A., Charles, M., Chatzi, L., Chevrier, C., Chrousos, G., et al. (2019) · BJOG: An International Journal of Obstetrics & Gynaecology

Gestational Diabetes Research and ManagementBirth, Development, and Health

Cited by 591

Genome-wide association study identifies sequence variants on 6q21 associated with age at menarche

Sulem, P., Gudbjartsson, D. F., Rafnar, T., Holm, H., Olafsdottir, E. J., Olafsdottir, G. H., Jonsson, T., Alexandersen, P., Feenstra, B., Boyd, H. A., et al. (2009) · Nature Genetics

Hypothalamic control of reproductive hormonesGenetic Associations and Epidemiology

Cited by 219

Gestational weight gain charts for different body mass index groups for women in Europe, North America, and Oceania

Santos, S., Eekhout, I., Voerman, E., Gaillard, R., Barros, H., Charles, M.-A., Chatzi, L., Chevrier, C., Chrousos, G. P., Corpeleijn, E., et al. (2018) · BMC Medicine

Gestational Diabetes Research and ManagementMaternal and Neonatal Healthcare

Cited by 133

Gonadal function in adult male patients with congenital adrenal hyperplasia

Engels, M., Gehrmann, K., Falhammar, H., Webb, E. A., Nordenström, A., Sweep, F. C., Span, P. N., van Herwaarden, A. E., Rohayem, J., Richter-Unruh, A., et al. (2018) · European Journal of Endocrinology

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 69

Phenotype in girls and women with Turner syndrome: association between dysmorphic features, karyotype and cardio-aortic malformations

Noordman, I., Duijnhouwer, A., Kapusta, L., Kempers, M., Roeleveld, N., Schokking, M., Smeets, D., Freriks, K., Timmers, H., & van Alfen-van der Velden, J. (2018) · European Journal of Medical Genetics

Genetic and Clinical Aspects of Sex Determination and Chromosomal AbnormalitiesSexual Differentiation and Disorders

Cited by 35

Exome chip association study excluded the involvement of rare coding variants with large effect sizes in the etiology of anorectal malformations

van de Putte, R., Wijers, C. H. W., Reutter, H., Vermeulen, S. H., Marcelis, C. L. M., Brosens, E., Broens, P. M. A., Homberg, M., Ludwig, M., Jenetzky, E., et al. (2019) · PLOS ONE

Congenital gastrointestinal and neural anomaliesGenetic Associations and Epidemiology

Cited by 6