D. Gerrelli

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FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder.

A. Monaco, S. Fisher, Cecilia S. L. Lai, 2003, Brain : a journal of neurology.

HDBR Expression: A Unique Resource for Global and Individual Gene Expression Studies during Early Human Brain Development

G. Clowry, A. Copp, D. Gerrelli, 2016, Front. Neuroanat..

Spatiotemporal expansion of primary progenitor zones in the developing human cerebellum

P. Hof, I. Glass, D. Gerrelli, 2019, Science.

Cardiovascular Defects Associated With Abnormalities in Midline Development in the Loop-tail Mouse Mutant

N. Greene, A. Copp, D. Gerrelli, 2001, Circulation research.

Integrated genome and transcriptome sequencing identifies a noncoding mutation in the genome replication factor DONSON as the cause of microcephaly-micromelia syndrome

Michael E. Coulter, C. Walsh, S. Wiemann, 2017, Genome research.

Mechanisms of normal and abnormal neurulation: evidence from embryo culture studies.

N. Greene, A. Copp, D. Gerrelli, 1997, The International journal of developmental biology.

Analysis of LIN28A in early human ovary development and as a candidate gene for primary ovarian insufficiency

M. Dattani, D. Gerrelli, G. Conway, 2012, Molecular and Cellular Endocrinology.

Mutations in CPAMD8 Cause a Unique Form of Autosomal-Recessive Anterior Segment Dysgenesis

D. Gerrelli, S. Tuft, V. Plagnol, 2016, American journal of human genetics.

Mutations in BMP4 cause eye, brain, and digit developmental anomalies: overlap between the BMP4 and hedgehog signaling pathways.

C. Ponting, H. Johansen-Berg, J. Klein, 2008, American journal of human genetics.

DEV122820 3073..3076

A. Copp, D. Gerrelli, S. Lindsay, 2015 .

Novel mutations in LHX3 are associated with hypopituitarism and sensorineural hearing loss.

M. Dattani, D. Gerrelli, H. Biebermann, 2008, Human molecular genetics.

SOX2 plays a critical role in the pituitary, forebrain, and eye during human embryonic development.

R. Lovell-Badge, Shuwen Huang, J. Crolla, 2008, The Journal of clinical endocrinology and metabolism.

Widespread dynamic and pleiotropic expression of the melanocortin‐1‐receptor (MC1R) system is conserved across chick, mouse and human embryonic development

D. Gerrelli, V. Kinsler, N. Solanky, 2017, bioRxiv.

CBP/p300-interacting transactivator, with Glu/Asp-rich C-terminal domain, 2, and pre-B-cell leukemia transcription factor 1 in human adrenal development and disease.

D. Gerrelli, F. Beuschlein, A. Huebner, 2009, The Journal of clinical endocrinology and metabolism.

CBP / p 300-Interacting Transactivator , with Glu / Asp-Rich C-Terminal Domain , 2 , and Pre-B-Cell Leukemia Transcription Factor 1 in Human Adrenal Development and Disease

D. Gerrelli, F. Beuschlein, A. Huebner, 2009 .

A genomic atlas of human adrenal and gonad development

Lin Lin, Dianne Gerrelli, Martino Barenco, 2017, Wellcome open research.

Human RSPO1/R-spondin1 Is Expressed during Early Ovary Development and Augments β-Catenin Signaling

D. Gerrelli, M. Mazzilli, P. Grammatico, 2011, PloS one.

Abnormalities of floor plate, notochord and somite differentiation in the loop-tail (Lp) mouse: a model of severe neural tube defects

Dianne Gerrelli, N. Greene, A. Copp, 1998, Mechanisms of Development.

Neurulation and neural tube closure defects.

A. Copp, D. Gerrelli, A. Fleming, 2000, Methods in molecular biology.

Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability

D. Pinto, S. Scherer, J. Sutcliffe, 2010, Journal of Medical Genetics.

Reduced TFAP2A function causes variable optic fissure closure and retinal defects and sensitizes eye development to mutations in other morphogenetic regulators

Tomas W. Fitzgerald, Stephen W. Wilson, N. Carter, 2009, Human Genetics.

Genomic organization and embryonic expression of igsf8, an immunoglobulin superfamily member implicated in development of the nervous system and organ epithelia

A. Copp, D. Gerrelli, P. Stanier, 2003, Molecular and Cellular Neuroscience.

Sonic hedgehog and the molecular regulation of mouse neural tube closure.

Patricia Ybot-Gonzalez, Dianne Gerrelli, A. Copp, 2002, Development.

Convergent extension, planar-cell-polarity signalling and initiation of mouse neural tube closure

N. Greene, A. Copp, D. Gerrelli, 2007, Development.

Heterozygous mutations of OTX2 cause severe ocular malformations.

B. Lorenz, S. Sisodiya, A. Fielder, 2005, American journal of human genetics.

De Novo Missense Variants in FBXW11 Cause Diverse Developmental Phenotypes Including Brain, Eye, and Digit Anomalies

Stephen W. Wilson, R. Holt, E. van Binsbergen, 2019, American journal of human genetics.

Transient expression of the conserved zinc finger gene INSM1 in progenitors and nascent neurons throughout embryonic and adult neurogenesis

D. Gerrelli, J. García-Añoveros, A. Duggan, 2008, The Journal of comparative neurology.

Endocrine effects of a single infection with Ostertagia ostertagi in the calf.

D. Gerrelli, A. Simmonds, I. Hart, 1987, International journal for parasitology.

Effect of diet on gastrin response to Ostertagia ostertagi infection in the calf.

D. Gerrelli, D. Jacobs, M. Fox, 1988, International journal for parasitology.

Ostertagia ostertagi infection in the calf: effects of a trickle challenge on appetite, digestibility, rate of passage of digesta and liveweight gain.

D. Gerrelli, D. Jacobs, M. Gill, 1989, Research in veterinary science.

Use of blood gastrin assay in the diagnosis of ovine haemonchiasis

D. Gerrelli, P. Goddard, D. Adhikari, 1988, Veterinary Record.

Common polymorphisms in the SERPINI2 gene are associated with refractive error in the 1958 British Birth Cohort.

P. Sham, D. Gerrelli, S. Bhattacharya, 2012, Investigative Ophthalmology and Visual Science.

Redefining the Etiologic Landscape of Cerebellar Malformations.

I. Krantz, D. Nickerson, G. Seelig, 2019, American journal of human genetics.

New variant and expression studies provide further insight into the genotype-phenotype correlation in YAP1-related developmental eye disorders

R. Holt, D. Gerrelli, D. Bax, 2017, Scientific Reports.

The Meckel-Gruber Syndrome proteins MKS1 and meckelin interact and are required for primary cilium formation.

Colin A. Johnson, K. Gull, A. Copp, 2007, Human molecular genetics.

Cordon-bleu is a conserved gene involved in neural tube formation.

J. Klingensmith, A. Copp, D. Gerrelli, 2003, Developmental biology.

Widespread dynamic and pleiotropic expression of the melanocortin-1-receptor (MC1R) system is conserved across chick, mouse and human embryonic development

D. Gerrelli, V. Kinsler, N. Solanky, 2017, bioRxiv.

Comparison of Iroquois gene expression in limbs/fins of vertebrate embryos

C. Tickle, L. Hurst, D. Gerrelli, 2010, Journal of anatomy.

Distinct expression patterns for type II topoisomerases IIA and IIB in the early foetal human telencephalon

G. Clowry, D. Gerrelli, L. Harkin, 2015, Journal of anatomy.

Enabling research with human embryonic and fetal tissue resources

Andrew J. Copp, Dianne Gerrelli, Susan Lindsay, 2015, Development.

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.

Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene.

P. Scambler, R. Hennekam, P. Hammond, 2009, American journal of human genetics.

Field evaluation of the oxfendazole pulse release bolus for the chemoprophylaxis of bovine parasitic gastroenteritis: a comparison with three other control strategies.

D. Gerrelli, D. Jacobs, M. Fox, 1987, Journal of veterinary pharmacology and therapeutics.

Effect of omeprazole treatment on feed intake and blood gastrin and pepsinogen levels in the calf.

D. Gerrelli, D. Jacobs, M. Fox, 1989, Research in veterinary science.

Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders

R. Holt, D. Gerrelli, D. Bax, 2016, Human Genetics.

Genetic enhancement of cognition in a kindred with cone–rod dystrophy due to RIMS1 mutation

I. Deary, A. Need, D. Goldstein, 2007, Journal of Medical Genetics.

Analysis of mouse models carrying the I26T and R160C substitutions in the transcriptional repressor HESX1 as models for septo-optic dysplasia and hypopituitarism

M. Dattani, D. Gerrelli, C. Andoniadou, 2008, Disease Models & Mechanisms.

The cardiac form of the tissue-specific SmN protein is identical to the brain and embryonic forms of the protein.

D. Gerrelli, D. Latchman, K. Grimaldi, 1993, Journal of molecular and cellular cardiology.

Cloning and sequencing of a mouse embryonal carcinoma cell mRNA encoding the tissue specific RNA splicing protein SmN.

D. Gerrelli, D. Latchman, N. Sharpe, 1991, Nucleic acids research.

Influence of an OPRB on immunity to gastrointestinal nematodes: a field study

D. Gerrelli, M. Fox, J. Pilkington, 1989, Veterinary Record.

Neuronal function of Tbx20 conserved from nematodes to vertebrates.

D. Gerrelli, A. Woollard, R. Pocock, 2008, Developmental biology.

The relationship between appetite and plasma non-esterified fatty acid levels in housed calves

D. Gerrelli, D. Jacobs, M. Fox, 2004, Veterinary Research Communications.

New variant and expression studies provide further insight into the genotype-phenotype correlation in YAP1-related developmental eye disorders

R. Holt, D. Gerrelli, D. Bax, 2017, Scientific Reports.

Ostertagia ostertagi infection in the calf: effects of a trickle challenge on the hormonal control of digestive and metabolic function.

D. Gerrelli, A. Simmonds, D. Jacobs, 1989, Research in veterinary science.

Endocrine effects of a trickle infection with Dictyocaulus viviparus in the calf.

D. Gerrelli, A. Simmonds, D. Jacobs, 1988, International journal for parasitology.

Failure of neural tube closure in the loop-tail (Lp) mutant mouse: analysis of the embryonic mechanism.

A. Copp, D. Gerrelli, 1997, Brain research. Developmental brain research.

The intronless mouse gene for the tissue specific splicing protein SmN is a processed pseudogene containing a stop codon after thirty-one amino acids.

D. Gerrelli, D. Latchman, K. Grimaldi, 1992, DNA sequence : the journal of DNA sequencing and mapping.

Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders

R. Holt, D. Gerrelli, D. Bax, 2016, Human Genetics.

Heterozygous mutations of OTX2 cause severe ocular malformations.

B. Lorenz, S. Sisodiya, A. Fielder, 2005, American journal of human genetics.

Antagonistic effects of retinoic acid and thyroid hormone on the expression of the tissue-specific splicing protein SmN in a clonal cell line derived from rat heart.

D. Gerrelli, D. Latchman, J. Huntriss, 1994, Journal of molecular and cellular cardiology.

Analysis of mouse models carrying the I 26 T and R 160 C substitutions in the transcriptional repressor HESX 1 as models for septo-optic dysplasia and hypopituitarism

Dianne Gerrelli, Massimo Signore, Juan Pedro Martinez-Barbera, 2022 .

CITED2 and PBX1 in human adrenal development and disease

D. Gerrelli, F. Beuschlein, A. Huebner, 2009 .