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D. Sparrow · SciRah

Researcher profile · Semantic Scholar

D. Sparrow

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D. Sparrow — researcher profile on SciRah

h-index: 38
Works: 72
Citations: 4,864

Most-cited papers

SmcHD1, containing a structural-maintenance-of-chromosomes hinge domain, has a critical role in X inactivation
M. Blewitt, Anne-Valerie Gendrel, Zhenyi Pang, D. Sparrow +8 more
2008Nature Genetics355 citations
Semantic Scholar
Mutation of the LUNATIC FRINGE gene in humans causes spondylocostal dysostosis with a severe vertebral phenotype.
D. Sparrow, G. Chapman, Merridee A. Wouters, N. Whittock +6 more
2006American Journal of Human Genetics251 citations Open access
Semantic Scholar
Axial skeletal defects caused by mutation in the spondylocostal dysplasia/pudgy gene Dll3 are associated with disruption of the segmentation clock within the presomitic mesoderm.
S. Dunwoodie, Melanie P. Clements, D. Sparrow, Xin Sa +2 more
2002Development230 citations
Semantic Scholar
NAD Deficiency, Congenital Malformations, and Niacin Supplementation
Hong-Jun Shi, Annabelle Enriquez, Melissa Rapadas, Ella M. M. A. Martin +29 more
2017New England Journal of Medicine222 citations Open access
Semantic Scholar
A mechanism for gene-environment interaction in the etiology of congenital scoliosis.
D. Sparrow, G. Chapman, Allanceson J. Smith, Muhammad Z. Mattar +10 more
2012Cell220 citations Open access
Semantic Scholar
MEF‐2 function is modified by a novel co‐repressor, MITR
D. Sparrow, E. Miska, E. Langley, Sorogini Reynaud-Deonauth +5 more
1999EMBO Journal218 citations Open access
Semantic Scholar
Ubc9p and the conjugation of SUMO-1 to RanGAP1 and RanBP2.
H. Saitoh, D. Sparrow, Tetsuo Shiomi, R. Pu +3 more
1998Current Biology205 citations Open access
Semantic Scholar
Notch inhibition by the ligand DELTA-LIKE 3 defines the mechanism of abnormal vertebral segmentation in spondylocostal dysostosis.
G. Chapman, D. Sparrow, E. Kremmer, S. Dunwoodie
2011Human Molecular Genetics192 citations Open access
Semantic Scholar
Evolution of distinct EGF domains with specific functions
Merridee A. Wouters, I. Rigoutsos, Carmen K. Chu, Li-Na L. Feng +2 more
2005Protein Science178 citations Open access
Semantic Scholar
Mutated MESP2 causes spondylocostal dysostosis in humans.
N. Whittock, D. Sparrow, Merridee A. Wouters, D. Sillence +3 more
2004American Journal of Human Genetics168 citations Open access
Semantic Scholar
Divergent functions and distinct localization of the Notch ligands DLL1 and DLL3 in vivo
Insa Geffers, Katrin Serth, G. Chapman, R. Jaekel +7 more
2007Journal of Cell Biology164 citations Open access
Semantic Scholar
The morphology of heart development in Xenopus laevis.
T. Mohun, L. Leong, W. Weninger, D. Sparrow
2000Developmental Biology140 citations Open access
Semantic Scholar
Mutation of Hairy-and-Enhancer-of-Split-7 in humans causes spondylocostal dysostosis.
D. Sparrow, E. Guillén-Navarro, D. Fatkin, S. Dunwoodie
2008Human Molecular Genetics138 citations
Semantic Scholar
Environmental Risk Factors for Congenital Heart Disease.
J. Kalisch-Smith, N. Ved, D. Sparrow
2019Cold Spring Harbor Perspectives in Biology137 citations Open access
Semantic Scholar
Loss of Cited2 affects trophoblast formation and vascularization of the mouse placenta.
S. Withington, A. Scott, D. Saunders, K. Floro +6 more
2006Developmental Biology121 citations Open access
Semantic Scholar
Autosomal dominant spondylocostal dysostosis is caused by mutation in TBX6.
D. Sparrow, A. McInerney-Leo, Z. Gucev, B. Gardiner +8 more
2013Human Molecular Genetics100 citations Open access
Semantic Scholar
Cited1 Is Required in Trophoblasts for Placental Development and for Embryo Growth and Survival
T. Rodríguez, D. Sparrow, A. Scott, S. Withington +7 more
2004Molecular and Cellular Biology100 citations Open access
Semantic Scholar
The Small Muscle-Specific Protein Csl Modifies Cell Shape and Promotes Myocyte Fusion in an Insulin-like Growth Factor 1–Dependent Manner
Steve Palmer, N. Groves, A. Schindeler, T. Yeoh +9 more
2001Journal of Cell Biology90 citations Open access
Semantic Scholar
A Screening Approach to Identify Clinically Actionable Variants Causing Congenital Heart Disease in Exome Data
J. Szot, H. Cuny, G. Blue, D. Humphreys +13 more
2018Circulation Genomic and Precision Medicine88 citations Open access
Semantic Scholar
Thylacine 1 is expressed segmentally within the paraxial mesoderm of the Xenopus embryo and interacts with the Notch pathway.
D. Sparrow, W. Jen, S. Kotecha, N. Towers +2 more
1998Development83 citations
Semantic Scholar
BMP/SMAD1 signaling sets a threshold for the left/right pathway in lateral plate mesoderm and limits availability of SMAD4.
Milena B. Furtado, Mark J. Solloway, Vanessa J. Jones, Mauro W. Costa +9 more
2008Genes & Development80 citations Open access
Semantic Scholar
Subdivision of the cardiac Nkx2.5 expression domain into myogenic and nonmyogenic compartments.
Michael Raffin, L. Leong, Melissa S. Rones, D. Sparrow +2 more
2000Developmental Biology73 citations Open access
Semantic Scholar
Two novel missense mutations in HAIRY-AND-ENHANCER-OF-SPLIT-7 in a family with spondylocostal dysostosis
D. Sparrow, D. Sillence, Merridee A. Wouters, P. Turnpenny +1 more
2010European Journal of Human Genetics62 citations Open access
Semantic Scholar
Regulation of the tinman homologues in Xenopus embryos.
D. Sparrow, Chengleng Cai, S. Kotecha, B. Latinkić +4 more
2000Developmental Biology61 citations Open access
Semantic Scholar
Tamoxifen administration in pregnant mice can be deleterious to both mother and embryo
N. Ved, Angela Curran, F. Ashcroft, D. Sparrow
2019Laboratory Animals. Journal of the Laboratory Animal Science Association60 citations Open access
Semantic Scholar
Loss of Cited2 causes congenital heart disease by perturbing left-right patterning of the body axis.
Kylie Lopes Floro, Stanley T Artap, J. Preis, D. Fatkin +6 more
2011Human Molecular Genetics59 citations
Semantic Scholar
Transcriptional regulation of the cardiac-specific MLC2 gene during Xenopus embryonic development
B. Latinkić, B. Cooper, Stuart J. Smith, S. Kotecha +3 more
2004Development59 citations Open access
Semantic Scholar
Xenopus eHAND: a marker for the developing cardiovascular system of the embryo that is regulated by bone morphogenetic proteins.
D. Sparrow, S. Kotecha, N. Towers, T. Mohun
1998Mechanisms of Development59 citations Open access
Semantic Scholar
Gene-environment interaction impacts on heart development and embryo survival
Julie L. M. Moreau, S. Kesteven, Ella M. M. A. Martin, Kin Lau +10 more
2019Development57 citations
Semantic Scholar
Cited2 is required in trophoblasts for correct placental capillary patterning.
Julie L. M. Moreau, Stanley T Artap, Hong-Jun Shi, G. Chapman +3 more
2014Developmental Biology54 citations Open access
Semantic Scholar
Gestational stress induces the unfolded protein response, resulting in heart defects
Hong-Jun Shi, Victoria C. O'Reilly, Julie L. M. Moreau, T. Bewes +8 more
2016Development53 citations Open access
Semantic Scholar
Distinct enhancers regulate skeletal and cardiac muscle-specific expression programs of the cardiac alpha-actin gene in Xenopus embryos.
B. Latinkić, B. Cooper, N. Towers, D. Sparrow +2 more
2002Developmental Biology52 citations Open access
Semantic Scholar
Cyclical expression of the Notch/Wnt regulator Nrarp requires modulation by Dll3 in somitogenesis
William F. Sewell, D. Sparrow, Allanceson J. Smith, Dorian M. Gonzalez +3 more
2009Developmental Biology48 citations Open access
Semantic Scholar
Functional genomics and gene-environment interaction highlight the complexity of Congenital Heart Disease caused by Notch pathway variants.
G. Chapman, Julie L. M. Moreau, E. Ip, J. Szot +18 more
2019Human Molecular Genetics47 citations Open access
Semantic Scholar
Complex SUMO-1 Regulation of Cardiac Transcription Factor Nkx2-5
Mauro W. Costa, S. Lee, Milena B. Furtado, Lia Xin +7 more
2011PLoS ONE46 citations Open access
Semantic Scholar
Compound heterozygous mutations in RIPPLY2 associated with vertebral segmentation defects.
A. McInerney-Leo, D. Sparrow, J. Harris, B. Gardiner +8 more
2015Human Molecular Genetics45 citations Open access
Semantic Scholar
Renal developmental defects resulting from in utero hypoxia are associated with suppression of ureteric β-catenin signaling.
Lorine Wilkinson, C. Neal, Reetu R. Singh, D. Sparrow +6 more
2015Kidney International44 citations Open access
Semantic Scholar
Maternal iron deficiency perturbs embryonic cardiovascular development in mice
J. Kalisch-Smith, N. Ved, D. Szumska, Jacob T. Munro +18 more
2021Nature Communications42 citations Open access
Semantic Scholar
Xenopus laevis transgenesis by sperm nuclear injection
Stuart J. Smith, L. Fairclough, B. Latinkić, D. Sparrow +1 more
2006Nature Protocols37 citations
Semantic Scholar
Mutation of HES7 in a large extended family with spondylocostal dysostosis and dextrocardia with situs inversus
D. Sparrow, E. Faqeih, B. Sallout, A. Alswaid +8 more
2013American Journal of Medical Genetics. Part A34 citations
Semantic Scholar
The Transcriptional Activity of CITED1 Is Regulated by Phosphorylation in a Cell Cycle-dependent Manner*
G. Shi, S. Boyle, D. Sparrow, S. Dunwoodie +2 more
2006Journal of Biological Chemistry33 citations Open access
Semantic Scholar
The MLC1v gene provides a transgenic marker of myocardium formation within developing chambers of the Xenopus heart
Stuart J. Smith, P. Ataliotis, S. Kotecha, N. Towers +2 more
2005Developmental Dynamics32 citations Open access
Semantic Scholar
Diverse requirements for Notch signalling in mammals.
D. Sparrow, Melanie P. Clements, S. Withington, A. Scott +5 more
2002International Journal of Developmental Biology31 citations
Semantic Scholar
The mouse notches up another success: understanding the causes of human vertebral malformation
D. Sparrow, G. Chapman, S. Dunwoodie
2011Mammalian Genome30 citations
Semantic Scholar
Autosomal dominant spondylocostal dysostosis in three generations of a Macedonian family: Negative mutation analysis of DLL3, MESP2, HES7, and LFNG
Z. Gucev, V. Tasic, N. Pop-Jordanova, D. Sparrow +4 more
2010American Journal of Medical Genetics. Part A29 citations
Semantic Scholar
Functional analysis of a gene-edited mouse model to gain insights into the disease mechanisms of a titin missense variant
He Jiang, C. Hooper, M. Kelly, V. Steeples +17 more
2021Basic Research in Cardiology28 citations Open access
Semantic Scholar
The onset of circulation triggers a metabolic switch required for endothelial to hematopoietic transition
Emanuele Azzoni, Vincent Frontera, Giorgio Anselmi, C. Rode +15 more
2021Cell Reports27 citations Open access
Semantic Scholar
Placental insufficiency associated with loss of Cited1 causes renal medullary dysplasia.
D. Sparrow, S. Boyle, Rebecca S. Sams, Bogdan Mazuruk +4 more
2009Journal of the American Society of Nephrology27 citations Open access
Semantic Scholar
Generation of conditional Cited2 null alleles
J. Preis, Natalie Wise, Mark J. Solloway, R. P. Harvey +2 more
2006Genesis27 citations
Semantic Scholar
Disruption of the somitic molecular clock causes abnormal vertebral segmentation.
D. Sparrow, G. Chapman, P. Turnpenny, S. Dunwoodie
2007Birth Defects Research Part C Embryo Today Reviews26 citations
Semantic Scholar

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S. Kotecha×7
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