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Minerva Carrasquillo

Research Profile

Genes & Molecular Sequences

Disorders

Procedures

Concepts & Ideas

Linkage Disequilibrium

Physiology

Chemicals & Drugs

Anatomy

Chromosomes, Human, Pair 13

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Publications

TOP 3
Nicola J Rutherford; Steven G Younkin; Gina Bisceglio; Minerva M Carrasquillo; Dennis W Dickson; Neill R Graff-Radford; Keith A Josephs; Ma Li; Joshua Menke; Joseph E Parisi; Ronald C Petersen; Rosa Rademakers
TMEM106B risk variant is implicated in the pathologic presentation of Alzheimer disease.
Hui Shi; Steven G Younkin; Olivia Belbin; Kristelle Brown; Minerva M Carrasquillo; Alison Goate; Noor Kalsheker; Simon Lovestone; Christopher Medway; Kevin Morgan; Peter Passmore; John Powell; Petroula Proitsi
Genetic variants influencing human aging from late-onset Alzheimer's disease (LOAD) genome-wide association studies (GWAS).
Gillian Hamilton; Richard Killick; Jean-Charles Lambert; V Shane Pankratz; Ronald C Petersen; John F Powell; Philippe Amouyel; Minerva M Carrasquillo; Dennis W Dickson; Neill R Graff-Radford; Steven G Younkin; Richard Wade-Martins
Functional and genetic analysis of haplotypic sequence variation at the nicastrin genomic locus.

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All Publications

2012: Nicola J Rutherford; Steven G Younkin; Gina Bisceglio; Minerva M Carrasquillo; Dennis W Dickson; Neill R Graff-Radford; Keith A Josephs; Ma Li; Joshua Menke; Joseph E Parisi; Ronald C Petersen; Rosa Rademakers
TMEM106B risk variant is implicated in the pathologic presentation of Alzheimer disease.
Neurology 2012;79(7):717-8.
2012: Hui Shi; Steven G Younkin; Olivia Belbin; Kristelle Brown; Minerva M Carrasquillo; Alison Goate; Noor Kalsheker; Simon Lovestone; Christopher Medway; Kevin Morgan; Peter Passmore; John Powell; Petroula Proitsi
Genetic variants influencing human aging from late-onset Alzheimer's disease (LOAD) genome-wide association studies (GWAS).
Neurobiology of aging 2012;33(8):1849.e5-18.
2012: Gillian Hamilton; Richard Killick; Jean-Charles Lambert; V Shane Pankratz; Ronald C Petersen; John F Powell; Philippe Amouyel; Minerva M Carrasquillo; Dennis W Dickson; Neill R Graff-Radford; Steven G Younkin; Richard Wade-Martins
Functional and genetic analysis of haplotypic sequence variation at the nicastrin genomic locus.
Neurobiology of aging 2012;33(8):1848.e1-13.
2012: Michael G Heckman; Minerva M Carrasquillo; Nancy N Diehl; Neill R Graff-Radford; Alexandra I Soto-Ortolaza; Ryan J Uitti; Zbigniew K Wszolek; Owen A Ross
Evaluation of the role of SNCA variants in survival without neurological disease.
PloS one 2012;7(8):e42877.
2012: Minerva M Carrasquillo; Kevin Morgan
Commentary on 'Functional analysis of APOE locus genetic variation implicates regional enhancers in the regulation of both TOMM40 and APOE'.
Journal of human genetics 2012;57(1):3-4.
2012: Mariet Allen; Olivia Belbin; Gina D Bisceglio; Minerva M Carrasquillo; Claire Cox; Oliver Culley; Dennis W Dickson; Neill R Graff-Radford; Chanley C Howell; Talisha A Hunter; Li Ma; Ronald C Petersen; Louise P Walker; Samantha L Wilcox; Steven G Younkin; Nilüfer Ertekin-Taner
Association and heterogeneity at the GAPDH locus in Alzheimer's disease.
Neurobiology of aging 2012;33(1):203.e25-33.
2011: Olivia Belbin; Minerva M Carrasquillo; Michael Crump; Oliver J Culley; Talisha A Hunter; Li Ma; Gina Bisceglio; Fanggeng Zou; Mariet Allen; dennis dickson; Neill R Graff-Radford; Ronald C. Petersen; Kevin Morgan; Steven G Younkin
Investigation of 15 of the top candidate genes for late-onset Alzheimer's disease.
Human genetics 2011;129(3):273-82.
2011: Minerva M Carrasquillo; Julia E Crook; Dennis W Dickson; Neill R Graff-Radford; Talisha A Hunter; Li Ma; Kevin Morgan; V Shane Pankratz; Peter Passmore; Ronald C Petersen; Sigrid B Sando; Zbigniew K Wszolek; Jan O Aasly; Maria Barcikowska; Olivia Belbin; Gina D Bisceglio; Fanggeng Zou; Steven G Younkin
Replication of EPHA1 and CD33 associations with late-onset Alzheimer's disease: a multi-centre case-control study.
Molecular neurodegeneration 2011;6(1):54.
2011: Olivia Belbin; Gina D Bisceglio; Minerva M Carrasquillo; Michael Crump; Kevin Morgan; Steven G Younkin
Multiple insulin degrading enzyme variants alter in vitro reporter gene expression.
PloS one 2011;6(6):e21429.
2011: James C Turton; Steven G Younkin; Ronald C. Petersen; Hui Shi; Olivia Belbin; Kristelle Brown; James Bullock; Minerva M Carrasquillo; dennis dickson; Neill R Graff-Radford; Noor Kalsheker; Christopher Medway; Kevin Morgan
Investigating statistical epistasis in complex disorders.
Journal of Alzheimer's disease : JAD 2011;25(4):635-44.
2011: Minerva M Carrasquillo; Julia E Crook; dennis dickson; Neill R Graff-Radford; Talisha A Hunter; Li Ma; Kevin Morgan; V Shane Pankratz; Ronald C. Petersen; Sigrid B Sando; Zbigniew K Wszolek; Jan O Aasly; Maria Barcikowska; Olivia Belbin; Gina D Bisceglio; Fanggeng Zou; Steven G Younkin
Replication of BIN1 association with Alzheimer's disease and evaluation of genetic interactions.
Journal of Alzheimer's disease : JAD 2011;24(4):751-8.
2011: Olivia Belbin; Kristelle Brown; Hui Shi; Christopher Medway; Richard Abraham; Peter Passmore; David Mann; A David Smith; Clive Holmes; Bernadette McGuinness; David Craig; Donald Warden; Reinhard Heun; Heike Kölsch; Seth Love; Noor Kalsheker; Julie Williams; Michael J Owen; Minerva M Carrasquillo; Steven G Younkin; Kevin Morgan; Patrick G Kehoe
A multi-center study of ACE and the risk of late-onset Alzheimer's disease.
Journal of Alzheimer's disease : JAD 2011;24(3):587-97.
2010: Minerva M Carrasquillo; Alexandra M Nicholson; NiCole Finch; J Raphael Gibbs; Matt Baker; Nicola J Rutherford; Talisha A Hunter; Mariely DeJesus-Hernandez; Gina D Bisceglio; Ian R Mackenzie; Andrew Singleton; Mark Cookson; Julia E Crook; Allissa Dillman; Dena Hernandez; Ronald C. Petersen; Neill R Graff-Radford; Steven G Younkin; Rosa Rademakers
Genome-wide screen identifies rs646776 near sortilin as a regulator of progranulin levels in human plasma.
American journal of human genetics 2010;87(6):890-7.
2003: Andy McCallion; Eileen Sproat Emison; Carl S Kashuk; R T Bush; M Kenton; Minerva M Carrasquillo; K W Jones; Giulia C Kennedy; Matthew E Portnoy; Eric Green; Aravinda Chakravarti
Genomic variation in multigenic traits: Hirschsprung disease.
Cold Spring Harbor symposia on quantitative biology 2003;68():373-81.
2003: B Engel-Yeger; S Zaaroura; Joël Zlotogora; Stavit A Shalev; Yasir Hujeirat; Minerva M Carrasquillo; B Saleh; Hillel Pratt
Otoacoustic emissions and brainstem evoked potentials in compound carriers of connexin 26 mutations.
Hearing research 2003;175(1-2):140-51.
2002: Minerva M Carrasquillo; Andy McCallion; Erik G Puffenberger; Carl S Kashuk; Nassim Nouri; Aravinda Chakravarti
Genome-wide association study and mouse model identify interaction between RET and EDNRB pathways in Hirschsprung disease.
Nature genetics 2002;32(2):237-44.
2002: B Engel-Yeger; S Zaaroura; Joël Zlotogora; Stavit A Shalev; Yasir Hujeirat; Minerva M Carrasquillo; Saleh Barges; Hillel Pratt
The effects of a connexin 26 mutation--35delG--on oto-acoustic emissions and brainstem evoked potentials: homozygotes and carriers.
Hearing research 2002;163(1-2):93-100.
2001: David J Cutler; Zwick Michael; Minerva M Carrasquillo; Chris T Yohn; K P Tobin; Carl S Kashuk; Debra J H Mathews; Nila A Shah; Evan E Eichler; J A Warrington; Aravinda Chakravarti
High-throughput variation detection and genotyping using microarrays.
Genome research 2001;11(11):1913-25.
1999: Peter J Harte; W Wu; Minerva M Carrasquillo; A Gregory Matera
Assignment of a novel bifurcated SET domain gene, SETDB1, to human chromosome band 1q21 by in situ hybridization and radiation hybrids.
Cytogenetics and cell genetics 1999;84(1-2):83-6.
1998: S H Shaw; Minerva M Carrasquillo; Carl S Kashuk; Erik G Puffenberger; Aravinda Chakravarti
Allele frequency distributions in pooled DNA samples: applications to mapping complex disease genes.
Genome research 1998;8(2):111-23.
1997: Minerva M Carrasquillo; Joël Zlotogora; Saleh Barges; Aravinda Chakravarti
Two different connexin 26 mutations in an inbred kindred segregating non-syndromic recessive deafness: implications for genetic studies in isolated populations.
Human molecular genetics 1997;6(12):2163-72.