Roger H Reeves
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Explore the profile of Roger H Reeves including associated specialties, affiliations and a list of published articles.
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90
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3485
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Recent Articles
11.
Wu D, Zhang Y, Cheng B, Mori S, Reeves R, Gao F
Brain Commun
. 2021 May;
3(2):fcab062.
PMID: 33937769
The cerebellum is a complex system with distinct cortical laminar organization. Alterations in cerebellar microstructure are common and associated with many factors such as genetics, cancer and ageing. Diffusion MRI...
12.
Channell M, Mattie L, Hamilton D, Capone G, Mahone E, Sherman S, et al.
J Neurodev Disord
. 2021 Apr;
13(1):16.
PMID: 33874886
Background: There is a high degree of inter- and intra-individual variability observed within the phenotype of Down syndrome. The Down Syndrome Cognition Project was formed to capture this variability by...
13.
Moyer A, Gardiner K, Reeves R
Trends Genet
. 2020 Oct;
37(5):444-459.
PMID: 33097276
Human chromosome 21 (Hsa21) contains more than 500 genes, making trisomy 21 one of the most complex genetic perturbations compatible with life. The ultimate goal of Down syndrome (DS) research...
14.
Trevino C, Holleman A, Corbitt H, Maslen C, Rosser T, Cutler D, et al.
Sci Rep
. 2020 Oct;
10(1):18051.
PMID: 33093519
Atrioventricular septal defects (AVSD) are a severe congenital heart defect present in individuals with Down syndrome (DS) at a > 2000-fold increased prevalence compared to the general population. This study...
15.
Kazuki Y, Gao F, Li Y, Moyer A, Devenney B, Hiramatsu K, et al.
Elife
. 2020 Jun;
9.
PMID: 32597754
Animal models of Down syndrome (DS), trisomic for human chromosome 21 (HSA21) genes or orthologs, provide insights into better understanding and treatment options. The only existing transchromosomic (Tc) mouse DS...
16.
Antonarakis S, Skotko B, Rafii M, Strydom A, Pape S, Bianchi D, et al.
Nat Rev Dis Primers
. 2020 Feb;
6(1):9.
PMID: 32029743
Trisomy 21, the presence of a supernumerary chromosome 21, results in a collection of clinical features commonly known as Down syndrome (DS). DS is among the most genetically complex of...
17.
Brose R, Savonenko A, Devenney B, Smith K, Reeves R
Front Aging Neurosci
. 2019 May;
11:96.
PMID: 31139073
Down syndrome (DS), a genetic disorder caused by partial or complete triplication of chromosome 21, is the most common genetic cause of intellectual disability. DS mouse models and cell lines...
18.
Reeves R, Delabar J, Potier M, Bhattacharyya A, Head E, Lemere C, et al.
Mol Syndromol
. 2019 Feb;
9(6):279-286.
PMID: 30800043
In the last decade, a number of important research advances in different fields have allowed Down syndrome (DS) research to flourish, creating a time of both unparalleled opportunity and considerable...
19.
Pitarresi J, Liu X, Avendano A, Thies K, Sizemore G, Hammer A, et al.
Life Sci Alliance
. 2018 Nov;
1(5):e201800190.
PMID: 30456390
The contribution of the tumor microenvironment to pancreatic ductal adenocarcinoma (PDAC) development is currently unclear. We therefore examined the consequences of disrupting paracrine Hedgehog (HH) signaling in PDAC stroma. Herein,...
20.
Rosser T, Edgin J, Capone G, Hamilton D, Allen E, Dooley K, et al.
Am J Intellect Dev Disabil
. 2018 Nov;
123(6):514-528.
PMID: 30421968
The cause of the high degree of variability in cognition and behavior among individuals with Down syndrome (DS) is unknown. We hypothesized that birth defects requiring surgery in the first...