L. Gregory

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The phenotypic spectrum associated with OTX2 mutations in humans

Jun Z. Li, M. Maghnie, M. Dattani, 2021, European journal of endocrinology.

Mutations in MAGEL2 and L1CAM are associated with congenital hypopituitarism and arthrogryposis.

H. Williams, M. Dattani, J. Hurst, 2018, The Journal of clinical endocrinology and metabolism.

TCF7L1 is involved in hypothalamo-pituitary axis development in mice and humans

Stephen W. Wilson, S. A. Jayakody, J. Martinez-Barbera, 2016 .

1 TCF 7 L 1 is involved in hypothalamo-pituitary axis development in mice and humans

Stephen W. Wilson, S. A. Jayakody, J. Martinez-Barbera, 2016 .

The molecular basis of congenital hypopituitarism and related disorders.

M. Dattani, L. Gregory, 2019, The Journal of clinical endocrinology and metabolism.

Transcription factor 7-like 1 is involved in hypothalamo–pituitary axis development in mice and humans

Stephen W. Wilson, S. A. Jayakody, M. Dattani, 2016, Proceedings of the National Academy of Sciences.

Structural Pituitary Abnormalities Associated With CHARGE Syndrome

M. Dattani, F. Bilan, M. McCabe, 2013, The Journal of clinical endocrinology and metabolism.

Variations in PROKR2, But Not PROK2, Are Associated With Hypopituitarism and Septo-optic Dysplasia

M. Dattani, M. Nagano, Y. Shigeyoshi, 2013, The Journal of clinical endocrinology and metabolism.

Genetic overlap in Kallmann syndrome, combined pituitary hormone deficiency, and septo-optic dysplasia.

S. Radovick, M. Dattani, R. Quinton, 2012, The Journal of clinical endocrinology and metabolism.

Partial Loss of Function of the GHRH Receptor Leads to Mild Growth Hormone Deficiency.

M. Dattani, P. Hindmarsh, J. Saldanha, 2016, The Journal of clinical endocrinology and metabolism.

Development of the Pituitary Gland.

M. Dattani, K. Alatzoglou, L. Gregory, 2020, Comprehensive Physiology.

Activating mutations in BRAF disrupt the hypothalamo-pituitary axis leading to hypopituitarism in mice and humans

M. Dattani, I. Robinson, J. Blackburn, 2021, Nature Communications.

BRAF mutations disrupt the hypothalamo-pituitary axis leading to hypopituitarism in mouse and humans 1

M. Dattani, I. Robinson, J. Blackburn, 2021 .

A recessive PRDM13 mutation results in congenital hypogonadotropic hypogonadism and cerebellar hypoplasia

H. Williams, M. Dattani, I. Robinson, 2021, medRxiv.

Embryologic and Genetic Disorders of the Pituitary Gland

M. Dattani, L. Gregory, 2019, Pituitary Disorders of Childhood.

Pituitary gland development: an update.

M. Dattani, M. McCabe, Rodrigo E. Bancalari, 2012, Endocrine development.

Pathogenic Variants in RNPC3 are Associated with Hypopituitarism and Primary Ovarian Insufficiency

M. Maghnie, S. Gustincich, M. Dattani, 2021, Genetics in medicine : official journal of the American College of Medical Genetics.

Neuropathy target esterase impairments cause Oliver–McFarlane and Laurence–Moon syndromes

M. Dattani, T. Révész, V. Plagnol, 2014, Journal of Medical Genetics.

Novel FGF8 mutations associated with recessive holoprosencephaly, craniofacial defects, and hypothalamo-pituitary dysfunction.

E. Puelles, M. Dattani, D. Gerrelli, 2011, The Journal of clinical endocrinology and metabolism.

Genetic screening in a large cohort of patients with congenital hypopituitarism; current knowledge and future directions

M. Dattani, M. McCabe, E. Webb, 2012 .

Impaired EIF2S3 function associated with a novel phenotype of X-linked hypopituitarism with glucose dysregulation

H. Williams, M. Dattani, I. Robinson, 2019, EBioMedicine.

Novel Lethal Form of Congenital Hypopituitarism Associated With the First Recessive LHX4 Mutation.

M. Dattani, M. McCabe, K. Humayun, 2015, The Journal of clinical endocrinology and metabolism.

The role of the sonic hedgehog signalling pathway in patients with midline defects and congenital hypopituitarism

M. Dattani, J. Saldanha, N. Canham, 2015, Clinical endocrinology.

HESX1 mutations in patients with congenital hypopituitarism: variable phenotypes with the same genotype

M. Dattani, S. Camper, B. Mendonca, 2016, Clinical endocrinology.

Loss-of-Function Variants in TBC1D32 Underlie Syndromic Hypopituitarism

M. Dattani, M. Varjosalo, T. Raivio, 2020, The Journal of clinical endocrinology and metabolism.

Novel application of luciferase assay for the in vitro functional assessment of KAL1 variants in three females with septo-optic dysplasia (SOD)

M. Dattani, J. Saldanha, S. Townshend, 2015, Molecular and Cellular Endocrinology.

The role of the sonic hedgehog signalling pathway in patients with midline defects and congenital hypopituitarism

M. Dattani, C. Andoniadou, M. Rossi, 2015, Clinical endocrinology.

Structural Pituitary Abnormalities Associated With CHARGE Syndrome

M. Dattani, F. Bilan, M. McCabe, 2013, Journal of Clinical Endocrinology and Metabolism.

This Work Is Licensed under a Creative Commons Attribution-noncommercial 3.0 Unported License Genetic Overlap in Kallmann Syndrome, Combined Pituitary Hormone Deficiency, and Septo-optic Dysplasia

S. Radovick, M. Dattani, R. Quinton, 2022 .