J. Morton

M. Kilby, J. Morton, E. Roberts, 2001, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Expanding the phenotype of biallelic loss‐of‐function variants in the NSUN2 gene: Description of four individuals with juvenile cataract, chronic nephritis, or brain anomaly as novel complications

J. Morton, A. Lehmann, S. Mizuno, 2020, American journal of medical genetics. Part A.

De Novo Variants in CNOT1, a Central Component of the CCR4-NOT Complex Involved in Gene Expression and RNA and Protein Stability, Cause Neurodevelopmental Delay.

L. Vissers, I. Krantz, R. Bodmer, 2020, American journal of human genetics.

D. Dunaway, S. Twigg, A. Wilkie, 2019, American journal of medical genetics. Part A.

Deep phenotyping of 14 new patients with IQSEC2 variants, including monozygotic twins of discordant phenotype

J. Clayton-Smith, K. Lachlan, J. Morton, 2019, Clinical genetics.

A case of recurrent congenital fetal anomalies associated with a familial subtelomeric translocation

J. Flint, S. Knight, M. Kilby, 1999, Prenatal diagnosis.

Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

Joshua C Randall, Tomas W. Fitzgerald, G. J. Swaminathan, 2018, Nature Communications.

COLEC10 is mutated in 3MC patients and regulates early craniofacial development

P. Beales, D. Jenkins, J. Morton, 2017, PLoS genetics.

Genotype-phenotype correlation between position of constitutional APC gene mutation and CHRPE expression in familial adenomatous polyposis

J. Neoptolemos, J. Morton, D. Morton, 1994, Human Genetics.

NCOR1/2 loss of function impairs memory through a novel GABAergic hypothalamus–CA3 projection

Zhandong Liu, Ying-Wooi Wan, J. Morton, 2018, Nature Neuroscience.

Germline pathogenic variants in HNRNPU are associated with alterations in blood methylome

H. Stewart, J. Morton, S. Lynch, 2023, European Journal of Human Genetics.

Familial Dandy–Walker syndrome: a case report supporting an autosomal inheritance

J. Morton, A. Hockley, T. Bragg, 2006, Child's Nervous System.

De novo mutations in MSL3 cause an X-linked syndrome marked by impaired histone H4 lysine 16 acetylation

R. Pfundt, J. Ganesh, B. Menten, 2018, Nature Genetics.

Author Correction: Loss of function of NCOR1 and NCOR2 impairs memory through a novel GABAergic hypothalamus–CA3 projection

Ying-Wooi Wan, J. Morton, X. Hou, 2019, Nature Neuroscience.

Micro syndrome in Muslim Pakistan children.

J. Morton, M. Henderson, J. Ainsworth, 2001, Ophthalmology.

Loss-of-function mutations in RAB18 cause Warburg micro syndrome.

Mark T. Handley, J. Graham, F. Müller, 2011, American journal of human genetics.

Clinical and molecular consequences of disease-associated de novo mutations in SATB2

Ibitoye, Fitzpatrick, Connell, 2017, Genetics in Medicine.

NCOR1/2 loss of function impairs memory through a novel GABAergic hypothalamus–CA3 projection

Zhandong, Ying-Wooi Wan, Gong, 2019 .

Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia.

G. Carvill, I. Scheffer, H. Mefford, 2019, American journal of human genetics.

Elucidating the genetic architecture of Adams–Oliver syndrome in a large European cohort

W. Reardon, F. McKenzie, P. Itin, 2018, Human mutation.