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Author Details

John J Farrell
Boston University Chobanian & Avedisian School of Medicine
2003
44
20
PMIDPaper TitleJournal TitlePublished Year
37578203DNA from multiple viral species is associated with Alzheimer's disease risk.Alzheimers Dement2024
37260021Novel loci for Alzheimer's disease identified by a genome-wide association study in Ashkenazi Jews.Alzheimers Dement2023
37745545Structural Variation Detection and Association Analysis of Whole-Genome-Sequence Data from 16,905 Alzheimer's Diseases Sequencing Project Subjects.medRxiv2023
37693521Association of Common and Rare Variants with Alzheimer's Disease in over 13,000 Diverse Individuals with Whole-Genome Sequencing from the Alzheimer's Disease Sequencing Project.medRxiv2023
34152079Association of mitochondrial variants and haplogroups identified by whole exome sequencing with Alzheimer's disease.Alzheimers Dement2022
36550123The impact of increasing levels of blood C-reactive protein on the inflammatory loci SPI1 and CD33 in Alzheimer's disease.Transl Psychiatry2022
35210353An association test of the spatial distribution of rare missense variants within protein structures identifies Alzheimer's disease-related patterns.Genome Res2022
33804025Set-Based Rare Variant Expression Quantitative Trait Loci in Blood and Brain from Alzheimer Disease Study Participants.Genes (Basel)2021
33907181Cell-type-specific expression quantitative trait loci associated with Alzheimer disease in blood and brain tissue.Transl Psychiatry2021
32541955A robust benchmark for detection of germline large deletions and insertions.Nat Biotechnol2020
32699374Author Correction: A robust benchmark for detection of germline large deletions and insertions.Nat Biotechnol2020
30503768A rare missense variant of CASP7 is associated with familial late-onset Alzheimer's disease.Alzheimers Dement2019
31648320BCL2L1 is associated with γ-globin gene expression.Blood Adv2019
30216683The association of HBG2, BCL11A, and HMIP polymorphisms with fetal hemoglobin and clinical phenotype in Iraqi Kurds with sickle cell disease.Int J Lab Hematol2019
31426376<i>APOE</i> Promoter Polymorphism-219T/G is an Effect Modifier of the Influence of <i>APOE</i> ε4 on Alzheimer's Disease Risk in a Multiracial Sample.J Clin Med2019
30924900Association of Rare Coding Mutations With Alzheimer Disease and Other Dementias Among Adults of European Ancestry.JAMA Netw Open2019
30624692PopCluster: an algorithm to identify genetic variants with ethnicity-dependent effects.Bioinformatics2019
29227829A long noncoding RNA from the HBS1L-MYB intergenic region on chr6q23 regulates human fetal hemoglobin expression.Blood Cells Mol Dis2018
30210277Targeted Sequencing of Alzheimer Disease Genes in African Americans Implicates Novel Risk Variants.Front Neurosci2018
28240767A variant Sp1 (R218Q) transcription factor might enhance HbF expression in β<sup>0</sup> -thalassaemia homozygotes.Br J Haematol2018
28612458Genetic determinants of HbF in Saudi Arabian and African Benin haplotype sickle cell anemia.Am J Hematol2017
28800727A phased SNP-based classification of sickle cell anemia HBB haplotypes.BMC Genomics2017
26771086The genetic basis of asymptomatic codon 8 frame-shift (HBB:c25_26delAA) β(0) -thalassaemia homozygotes.Br J Haematol2016
27501013A candidate transacting modulator of fetal hemoglobin gene expression in the Arab-Indian haplotype of sickle cell anemia.Am J Hematol2016
27185208Homozygosity for a haplotype in the HBG2-OR51B4 region is exclusive to Arab-Indian haplotype sickle cell anemia.Am J Hematol2016
27282567Variants of ZBTB7A (LRF) and its β-globin gene cluster binding motifs in sickle cell anemia.Blood Cells Mol Dis2016
25703683BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia.Blood Cells Mol Dis2015
24439028Search for age-related macular degeneration risk variants in Alzheimer disease genes and pathways.Neurobiol Aging2014
25172201Two rare AKAP9 variants are associated with Alzheimer's disease in African Americans.Alzheimers Dement2014
23465615Fetal hemoglobin in sickle cell anemia: genetic studies of the Arab-Indian haplotype.Blood Cells Mol Dis2013
22641479A functional promoter polymorphism of the δ-globin gene is a specific marker of the Arab-Indian haplotype.Am J Hematol2012
21385855A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expression.Blood2011
18266208Variation and heritability of Hb F and F-cells among beta-thalassemia heterozygotes in Hong Kong.Am J Hematol2008
17299377Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea.Pharmacogenomics J2007
16681647Sickle cell leg ulcers: associations with haemolysis and SNPs in Klotho, TEK and genes of the TGF-beta/BMP pathway.Br J Haematol2006
16886151Association of polymorphisms of IGF1R and genes in the transforming growth factor- beta /bone morphogenetic protein pathway with bacteremia in sickle cell anemia.Clin Infect Dis2006
15784727Association of klotho, bone morphogenic protein 6, and annexin A2 polymorphisms with sickle cell osteonecrosis.Blood2005
16451694Genome-wide linkage analysis for alcohol dependence: a comparison between single-nucleotide polymorphism and microsatellite marker assays.BMC Genet2005
16451610Whole-genome variance components linkage analysis using single-nucleotide polymorphisms versus microsatellites on quantitative traits of derived phenotypes from factor analysis of electroencephalogram waves.BMC Genet2005
16451606Multifactor-dimensionality reduction versus family-based association tests in detecting susceptibility loci in discordant sib-pair studies.BMC Genet2005
15638863Association of single nucleotide polymorphisms in klotho with priapism in sickle cell anaemia.Br J Haematol2005
15040424Polymorphisms near a chromosome 6q QTL area are associated with modulation of fetal hemoglobin levels in sickle cell anemia.Cell Mol Biol (Noisy-le-grand)2004
14975083Empirically derived phenotypic subgroups - qualitative and quantitative trait analyses.BMC Genet2003
14975168Search for genetic factors predisposing to atherogenic dyslipidemia.BMC Genet2003
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Collaborators

Lindsay A Farrer
Boston University Chobanian & Avedisian School of Medicine
Co-authored papers 33
Paola Sebastiani
Institute for Clinical Research and Health Policy Studies, Tufts Medical Center
Co-authored papers 12
Kathryn L Lunetta
Co-authored papers 11
Xiaoling Zhang
Co-authored papers 8
Jonathan L Haines
Cleveland Institute for Computational Biology, Case Western Reserve University
Co-authored papers 8
Gerard D Schellenberg
Co-authored papers 8
Margaret A Pericak-Vance
Co-authored papers 7
Badri N Vardarajan
Columbia University Irving Medical Center, New York Presbyterian Hospital
Co-authored papers 6
Li-San Wang
Co-authored papers 5
William S Bush
Cleveland Institute for Computational Biology, Case Western Reserve University
Co-authored papers 3
Jae Yoon Chung
Boston University School of Medicine
Co-authored papers 3
Nasir A S Al-Allawi
College of Medicine, University of Duhok
Co-authored papers 3
Yi Yu
Tufts Medical Center
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Yan Meng
Co-authored papers 3
Nancy F Hansen
National Human Genome Research Institute, National Institutes of Health
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Xian Fan
Rice University
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Adam M Phillippy
National Human Genome Research Institute, National Institutes of Health
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Alvaro Martinez Barrio
Uppsala University
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Noah Spies
Stanford University
Co-authored papers 2
Stephen T Sherry
National Center for Biotechnology Information, National Institutes of Health
Co-authored papers 2
Ian T Fiddes
Liver Center and Diabetes Center, University of California san francisco
Co-authored papers 2
Noushin Ghaffari
Prairie View A&M University
Co-authored papers 2
Nathan D Olson
National Institute of Standards and Technology
Co-authored papers 2
Adam C English
Baylor College of Medicine Human Genome Sequencing Center
Co-authored papers 2
Chunlin Xiao
Chongqing Aier Eye Hospital
Co-authored papers 2
Weichen Zhou
Chengdu First People's Hospital
Co-authored papers 2
Ken Chen
University of Texas MD Anderson Cancer Center
Co-authored papers 2
Ryan E Mills
University of Michigan Medical School ann arbor
Co-authored papers 2
Alexandre Rouette
Charles-Bruneau Cancer Center, Centre Hospitalier Universitaire (CHU) Sainte-Justine
Co-authored papers 2
Camir Ricketts
Institute for Computational Biomedicine, Weill Cornell Medicine of Cornell University
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