Hardelin, Jean-Pierre

European Consensus Statement on congenital hypogonadotropic hypogonadism—pathogenesis, diagnosis and treatment

Boehm, U., Bouloux, P.-M., Dattani, M. T., de Roux, N., Dodé, C., Dunkel, L., Dwyer, A. A., Giacobini, P., Hardelin, J.-P., Juul, A., et al. (2015) · Nature Reviews Endocrinology

Hypothalamic control of reproductive hormonesSexual Differentiation and Disorders

Cited by 874

The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules

Legouis, R., Hardelin, J.-P., Levilliers, J., Claverie, J.-M., Compain, S., Wunderle, V., Millasseau, P., Le Paslier, D., Cohen, D., & Caterina, D. (1991) · Cell

Hypothalamic control of reproductive hormonesGenetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Cited by 678

Kallmann Syndrome: Mutations in the Genes Encoding Prokineticin-2 and Prokineticin Receptor-2

Dodé, C., Teixeira, L., Levilliers, J., Fouveaut, C., Bouchard, P., Kottler, M.-L., Lespinasse, J., Lienhardt-Roussie, A., Mathieu, M., Moerman, A., et al. (2006) · PLoS Genetics

Hypothalamic control of reproductive hormonesOlfactory and Sensory Function Studies

Cited by 457

Dual AAV-mediated gene therapy restores hearing in a DFNB9 mouse model

Akil, O., Dyka, F., Calvet, C., Emptoz, A., Lahlou, G., Nouaille, S., Boutet de Monvel, J., Hardelin, J.-P., Hauswirth, W. W., Avan, P., et al. (2019) · Proceedings of the National Academy of Sciences

Hearing, Cochlea, Tinnitus, GeneticsVirus-based gene therapy research

Cited by 300

SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome

Hanchate, N. K., Giacobini, P., Lhuillier, P., Parkash, J., Espy, C., Fouveaut, C., Leroy, C., Baron, S., Campagne, C., Vanacker, C., et al. (2012) · PLoS Genetics

Hypothalamic control of reproductive hormonesOlfactory and Sensory Function Studies

Cited by 217

Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndrome

Hardelin, J.-P., Levilliers, J., Blanchard, S., Carel, J.-C., Leutenegger, M., Pinard-Bertelletto, J.-P., Bouloux, P., & Petit, C. (1993) · Human Molecular Genetics

Hypothalamic control of reproductive hormonesGenetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Cited by 203

Kallmann syndrome: 14 novel mutations in KAL1 and FGFR1(KAL2): MUTATIONS IN BRIEF

Albuisson, J., Pêcheux, C., Carel, J.-C., Lacombe, D., Leheup, B., Lapuzina, P., Bouchard, P., Legius, E., Matthijs, G., Wasniewska, M., et al. (2005) · Human Mutation

Hypothalamic control of reproductive hormonesPituitary Gland Disorders and Treatments

Cited by 146

Nicotine inhibits the VTA-to-amygdala dopamine pathway to promote anxiety

Nguyen, C., Mondoloni, S., Le Borgne, T., Centeno, I., Come, M., Jehl, J., Solié, C., Reynolds, L. M., Durand-de Cuttoli, R., Tolu, S., et al. (2021) · Neuron

Neurotransmitter Receptor Influence on BehaviorNicotinic Acetylcholine Receptors Study

Cited by 136

PROKR2 missense mutations associated with Kallmann syndrome impair receptor signalling activity

Monnier, C., Dodé, C., Fabre, L., Teixeira, L., Labesse, G., Pin, J.-P., Hardelin, J.-P., & Rondard, P. (2009) · Human Molecular Genetics

Hypothalamic control of reproductive hormonesReceptor Mechanisms and Signaling

Cited by 123

Biallelic mutations in the prokineticin-2 gene in two sporadic cases of Kallmann syndrome

Leroy, C., Fouveaut, C., Leclercq, S., Jacquemont, S., Boullay, H. D., Lespinasse, J., Delpech, M., Dupont, J.-M., Hardelin, J.-P., & Dodé, C. (2008) · European Journal of Human Genetics

Hypothalamic control of reproductive hormonesGenetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Cited by 48