List of works - Susan Lindsay

3 dimensional modelling of early human brain development using optical projection tomography

scientific article

3D modelling, gene expression mapping and post-mapping image analysis in the developing human brain.

scientific article published in September 2005

A comparative proteomic analysis of human and rat embryonic cerebrospinal fluid.

scientific article published on 16 August 2007

A giant novel gene undergoing extensive alternative splicing is severed by a Cornelia de Lange-associated translocation breakpoint at 3q26.3.

scientific article published on 27 May 2004

A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis

scientific article

A mutation hot spot for nonspecific X-linked mental retardation in the MECP2 gene causes the PPM-X syndrome

scientific article published on 15 February 2002

A novel mammalian wnt gene, WNT8B, shows brain-restricted expression in early development, with sharply delimited expression boundaries in the developing forebrain

scientific article

A study of X chromosome activity in two incontinentia pigmenti families with probable linkage to Xq28

scientific article published on 01 January 1994

Abnormal retinal development associated with FRMD7 mutations.

scientific article

An integrated transcriptional analysis of the developing human retina

scientific article published on 29 January 2019

Anatomical and gene expression mapping of the ventral pallium in a three-dimensional model of developing human brain.

scientific article

Characterisation of Wnt gene expression during the differentiation of murine embryonic stem cells in vitro: role of Wnt3 in enhancing haematopoietic differentiation.

scientific article

Charting the protomap of the human telencephalon

scientific article

Corrigendum: Neurexins 1-3 Each Have a Distinct Pattern of Expression in the Early Developing Human Cerebral Cortex

scientific article published on 01 April 2019

Craniofacial expression of human and murine TBX22 correlates with the cleft palate and ankyloglossia phenotype observed in CPX patients.

scientific article

Crossover analysis in a British family suggests that Coffin-Lowry syndrome maps to a 3.4-cM interval in Xp22.

scientific article published in December 1995

Decoding human fetal liver haematopoiesis

scientific article published on 09 October 2019

Differences in methylation on the active and inactive human X chromosomes

scientific article published on 01 May 1985

Dinucleotide repeat polymorphism at the DXS559 locus

scientific article published on December 1, 1992

Dinucleotide repeat polymorphism at the DXS573 locus.

scientific article

Disrupted alternative splicing for genes implicated in splicing and ciliogenesis causes PRPF31 retinitis pigmentosa ⬇️

scientific article published in Nature Communications

Distinct cortical and sub-cortical neurogenic domains for GABAergic interneuron precursor transcription factors NKX2.1, OLIG2 and COUP-TFII in early fetal human telencephalon.

scientific article published on 30 November 2016

Enabling research with human embryonic and fetal tissue resources.

scientific article

Expression of PLA2G6 in human fetal development: Implications for infantile neuroaxonal dystrophy ⬇️

scientific article published on September 9, 2010

Extracellular matrix component expression in human pluripotent stem cell-derived retinal organoids recapitulates retinogenesis in vivo and reveals an important role for IMPG1 and CD44 in the development of photoreceptors and interphotoreceptor matri

scientific article published on 17 May 2018

FISH mapping of 22 novel X chromosome cosmids and the isolation of a novel microsatellite on proximal Xp

scientific article published on 01 January 1995

From spatial-data to 3D models of the developing human brain.

scientific article

Gene expression across mammalian organ development

scientific article published on 26 June 2019

Genetic and physical mapping around the properdin P gene

scientific article

Genetic and physical mapping of five novel microsatellite markers on human Xp21.1-p11.22

scientific article published on 01 January 1995

Genetic mapping of a cone and rod dysfunction (Aland Island eye disease) to the proximal short arm of the human X chromosome.

scientific article

Glypican 3 and glypican 4 are juxtaposed in Xq26.1

scientific article

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

scientific article published on 26 October 2016

Hepatic differentiation of murine embryonic stem cells

scientific article (publication date: 2002)

Human CHN1 mutations hyperactivate alpha2-chimaerin and cause Duane's retraction syndrome

scientific article

Human-mouse differences in the embryonic expression patterns of developmental control genes and disease genes.

scientific article published in January 2000

Investigating embryonic expression patterns and evolution of AHI1 and CEP290 genes, implicated in Joubert syndrome

scientific article

Investigating gradients of gene expression involved in early human cortical development.

scientific article

Isolation and characterization of WNT8B, a novel human Wnt gene that maps to 10q24.

scientific article

Isolation and characterization of three microsatellite markers in the proximal long arm of the human X chromosome

scientific article published on 01 July 1993

Isolation, characterisation and embryonic expression of WNT11, a gene which maps to 11q13.5 and has possible roles in the development of skeleton, kidney and lung

scientific article

JAtlasView: a Java atlas-viewer for browsing biomedical 3D images and atlases

scientific article

Laminin γ3 plays an important role in retinal lamination, photoreceptor organisation and ganglion cell differentiation.

scientific article

Large scale deletions in the GPC3 gene may account for a minority of cases of Simpson-Golabi-Behmel syndrome.

scientific article published on June 1997

Localisation of the gene for Norrie disease to between DXS7 and DXS426 on Xp

scientific article published on 01 January 1992

Localization of the microsatellite probe DXS426 between DXS7 and DXS255 on Xp and linkage to X-linked retinitis pigmentosa

scientific article

MRC-Wellcome Trust Human Developmental Biology Resource: enabling studies of human developmental gene expression.

scientific article

Mapping human development at single-cell resolution.

scientific article published on 8 February 2018

Neurexins 1-3 Each Have a Distinct Pattern of Expression in the Early Developing Human Cerebral Cortex.

scientific article published on 23 December 2016

Neurodevelopmental protein Musashi 1 interacts with the Zika genome and promotes viral replication ⬇️

scientific article

Partial cloning and assignment of WNT6 to human chromosome band 2q35 by in situ hybridization

scientific article

SRY, SOX9, and DAX1 expression patterns during human sex determination and gonadal development

scientific article

Spatiotemporal immune zonation of the human kidney

scientific article

Subplate in the developing cortex of mouse and human

scientific article published on 18 August 2010

The HUDSEN Atlas: a three-dimensional (3D) spatial framework for studying gene expression in the developing human brain.

scientific article

The Transcription Factors COUP-TFI and COUP-TFII have Distinct Roles in Arealisation and GABAergic Interneuron Specification in the Early Human Fetal Telencephalon

scientific article published in October 2017

The corticofugal neuron-associated genes ROBO1, SRGAP1, and CTIP2 exhibit an anterior to posterior gradient of expression in early fetal human neocortex development.

scientific article

The early fetal development of human neocortical GABAergic interneurons

scientific article

The gene for Aarskog syndrome is located between DXS255 and DXS566 (Xp11.2-Xq13).

scientific article published in October 1992

The nystagmus-associated FRMD7 gene regulates neuronal outgrowth and development

scientific journal article

The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome.

scientific article

The tissue-specific RNA binding protein T-STAR controls regional splicing patterns of neurexin pre-mRNAs in the brain

scientific article

Til 1--a human lymphoblastoid cell line with minimal DNA methylation

scientific article published on 01 February 1989

Two dinucleotide repeat polymorphisms at the DXS571 locus

scientific article published on December 1, 1992

Ultrahigh thermal conductivity confirmed in boron arsenide

scientific article

Utrophin mRNA Expression in Muscle Is Not Restricted to the Neuromuscular Junction ⬇️

scientific article published on April 1, 1998

X chromosome linkage studies in familial Rett syndrome

scientific article published on 01 January 1993

List of works by Susan Lindsay

3 dimensional modelling of early human brain development using optical projection tomography

3D modelling, gene expression mapping and post-mapping image analysis in the developing human brain.

A comparative proteomic analysis of human and rat embryonic cerebrospinal fluid.

A giant novel gene undergoing extensive alternative splicing is severed by a Cornelia de Lange-associated translocation breakpoint at 3q26.3.

A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis

A mutation hot spot for nonspecific X-linked mental retardation in the MECP2 gene causes the PPM-X syndrome

A novel mammalian wnt gene, WNT8B, shows brain-restricted expression in early development, with sharply delimited expression boundaries in the developing forebrain

A study of X chromosome activity in two incontinentia pigmenti families with probable linkage to Xq28

Abnormal retinal development associated with FRMD7 mutations.

An integrated transcriptional analysis of the developing human retina

Anatomical and gene expression mapping of the ventral pallium in a three-dimensional model of developing human brain.

Characterisation of Wnt gene expression during the differentiation of murine embryonic stem cells in vitro: role of Wnt3 in enhancing haematopoietic differentiation.

Charting the protomap of the human telencephalon

Corrigendum: Neurexins 1-3 Each Have a Distinct Pattern of Expression in the Early Developing Human Cerebral Cortex

Craniofacial expression of human and murine TBX22 correlates with the cleft palate and ankyloglossia phenotype observed in CPX patients.

Crossover analysis in a British family suggests that Coffin-Lowry syndrome maps to a 3.4-cM interval in Xp22.

Decoding human fetal liver haematopoiesis

Differences in methylation on the active and inactive human X chromosomes

Dinucleotide repeat polymorphism at the DXS559 locus

Dinucleotide repeat polymorphism at the DXS573 locus.

Disrupted alternative splicing for genes implicated in splicing and ciliogenesis causes PRPF31 retinitis pigmentosa ⬇️

Distinct cortical and sub-cortical neurogenic domains for GABAergic interneuron precursor transcription factors NKX2.1, OLIG2 and COUP-TFII in early fetal human telencephalon.

Enabling research with human embryonic and fetal tissue resources.

Expression of PLA2G6 in human fetal development: Implications for infantile neuroaxonal dystrophy ⬇️

Extracellular matrix component expression in human pluripotent stem cell-derived retinal organoids recapitulates retinogenesis in vivo and reveals an important role for IMPG1 and CD44 in the development of photoreceptors and interphotoreceptor matri

FISH mapping of 22 novel X chromosome cosmids and the isolation of a novel microsatellite on proximal Xp

From spatial-data to 3D models of the developing human brain.

Gene expression across mammalian organ development

Genetic and physical mapping around the properdin P gene

Genetic and physical mapping of five novel microsatellite markers on human Xp21.1-p11.22

Genetic mapping of a cone and rod dysfunction (Aland Island eye disease) to the proximal short arm of the human X chromosome.

Glypican 3 and glypican 4 are juxtaposed in Xq26.1

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

Hepatic differentiation of murine embryonic stem cells

Human CHN1 mutations hyperactivate alpha2-chimaerin and cause Duane's retraction syndrome

Human-mouse differences in the embryonic expression patterns of developmental control genes and disease genes.

Investigating embryonic expression patterns and evolution of AHI1 and CEP290 genes, implicated in Joubert syndrome

Investigating gradients of gene expression involved in early human cortical development.

Isolation and characterization of WNT8B, a novel human Wnt gene that maps to 10q24.

Isolation and characterization of three microsatellite markers in the proximal long arm of the human X chromosome

Isolation, characterisation and embryonic expression of WNT11, a gene which maps to 11q13.5 and has possible roles in the development of skeleton, kidney and lung

JAtlasView: a Java atlas-viewer for browsing biomedical 3D images and atlases

Laminin γ3 plays an important role in retinal lamination, photoreceptor organisation and ganglion cell differentiation.

Large scale deletions in the GPC3 gene may account for a minority of cases of Simpson-Golabi-Behmel syndrome.

Localisation of the gene for Norrie disease to between DXS7 and DXS426 on Xp

Localization of the microsatellite probe DXS426 between DXS7 and DXS255 on Xp and linkage to X-linked retinitis pigmentosa

MRC-Wellcome Trust Human Developmental Biology Resource: enabling studies of human developmental gene expression.

Mapping human development at single-cell resolution.

Neurexins 1-3 Each Have a Distinct Pattern of Expression in the Early Developing Human Cerebral Cortex.

Neurodevelopmental protein Musashi 1 interacts with the Zika genome and promotes viral replication ⬇️

Partial cloning and assignment of WNT6 to human chromosome band 2q35 by in situ hybridization

SRY, SOX9, and DAX1 expression patterns during human sex determination and gonadal development

Spatiotemporal immune zonation of the human kidney

Subplate in the developing cortex of mouse and human

The HUDSEN Atlas: a three-dimensional (3D) spatial framework for studying gene expression in the developing human brain.

The Transcription Factors COUP-TFI and COUP-TFII have Distinct Roles in Arealisation and GABAergic Interneuron Specification in the Early Human Fetal Telencephalon

The corticofugal neuron-associated genes ROBO1, SRGAP1, and CTIP2 exhibit an anterior to posterior gradient of expression in early fetal human neocortex development.

The early fetal development of human neocortical GABAergic interneurons

The gene for Aarskog syndrome is located between DXS255 and DXS566 (Xp11.2-Xq13).

The nystagmus-associated FRMD7 gene regulates neuronal outgrowth and development

The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome.

The tissue-specific RNA binding protein T-STAR controls regional splicing patterns of neurexin pre-mRNAs in the brain

Til 1--a human lymphoblastoid cell line with minimal DNA methylation

Two dinucleotide repeat polymorphisms at the DXS571 locus

Ultrahigh thermal conductivity confirmed in boron arsenide

Utrophin mRNA Expression in Muscle Is Not Restricted to the Neuromuscular Junction ⬇️

X chromosome linkage studies in familial Rett syndrome