Deborah Morrogh - Concepedia

Author

Deborah Morrogh

Also Known As

Alison Male, Ana Beleza, D Morrogh, D. Morrogh, Deborah M. Morrogh, Deborah Morrogh, Morrogh, D, Morrogh, D., Simon J H Heales

Publications

2.2K

Citations

H-Index

Concepts

All Affiliations

University College London Great Ormond Street Hospital Wessex Regional Genetics Laboratory Great Ormond Street Hospital for Children NHS Foundation Trust Sheffield Children's Hospital

About

Deborah Morrogh is an author at University College London specializing in medicine, genetics, and schizophrenia.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	265
2	Social Sciences	2	2	71
3	Molecular Genetics	1	1	161
4	Molecular Medicine	1	1	161
5	Neurology	1	1	40

Deborah Morrogh

Publications

1.1K

Citations

H-Index

Page 1

	Year	Citations
Multiple Congenital Melanocytic Nevi and Neurocutaneous Melanosis Are Caused by Postzygotic Mutations in Codon 61 of NRAS Veronica A. Kinsler, Anna Thomas, Miho Ishida, Journal of Investigative Dermatology	2013	343
Improving diagnosis and broadening the phenotypes in early-onset seizure and severe developmental delay disorders through gene panel analysis Natalie Trump, Amy McTague, Helen Brittain, Journal of Medical Genetics	2016	206
Somatic mutations and progressive monosomy modify SAMD9-related phenotypes in humans Federica Buonocore, Peter Kühnen, Jenifer P. Suntharalingham, Journal of Clinical Investigation GeneticsGenetic EpidemiologyMolecular GeneticsDisease Gene IdentificationClinical Genetics	2017	161
Mutations in SNX14 Cause a Distinctive Autosomal-Recessive Cerebellar Ataxia and Intellectual Disability Syndrome Anna Thomas, Hywel Williams, Núria Setó‐Salvia, The American Journal of Human Genetics	2014	100
Clinical and immunological features in a cohort of patients with partial DiGeorge syndrome followed at a single center Giuliana Giardino, Nesrine Radwan, Patra Koletsi, Blood	2019	65
Chromosomal microarray testing in adults with intellectual disability presenting with comorbid psychiatric disorders Kate Wolfe, André Strydom, Deborah Morrogh, European Journal of Human Genetics Psychiatric DisordersGeneticsComorbid Psychiatric DisordersGenomicsDisease Gene Identification	2016	40
Sotos syndrome, infantile hypercalcemia, and nephrocalcinosis: a contiguous gene syndrome Janna Kenny, Melissa Lees, Susan Drury, Pediatric Nephrology Developmental AnomalyMendelian DisorderGenetic DisorderGeneticsInherited Metabolic Disease	2011	33
The instability of the BTB-KELCH protein Gigaxonin causes Giant Axonal Neuropathy and constitutes a new penetrant and specific diagnostic test Alexia Boizot, Yasmina Talmat-Amar, Deborah Morrogh, Acta Neuropathologica Communications	2014	33
Delineating the psychiatric and behavioral phenotype of recurrent 2q13 deletions and duplications Kate Wolfe, Andrew McQuillin, Viola Alesi, American Journal of Medical Genetics Part B Neuropsychiatric Genetics GeneticsDisease Gene IdentificationGenomicsPsychologySocial Sciences	2018	31
X-linked intellectual disability type Nascimento is a clinically distinct, probably underdiagnosed entity Johanna Christina Czeschik, Peter Bauer, Karin Buiting, Orphanet Journal of Rare Diseases	2013	26

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