jclau's genetics [30 articles] Export

Recent papers added to jclau's library classified by the tag genetics. You can also see everyone's genetics.

	Prenatal sex differences in the human brain [My Copy] Mol Psychiatry, Vol. 14, No. 11. (01 November 2009), pp. 988-989. by B. Reinius, E. Jazin posted to prenatal human genetics gene-expression gender dimorphism differences development brain bioinformatics by jclau on 2009-10-24 15:49:11 as
	Genetic dissection of the mouse CNS using magnetic resonance microscopy. [My Copy] Current opinion in neurology, Vol. 22, No. 4. (August 2009), pp. 379-386. by Alexandra Badea, G. Allan Johnson, Robert W. Williams posted to vbm review neurodegenerative mouse morphometry imaging genetics dbm brain alzheimers by jclau on 2009-10-17 02:25:48 as
	Finding the missing heritability of complex diseases. [My Copy] Nature, Vol. 461, No. 7265. (8 October 2009), pp. 747-753. by Teri A. Manolio, Francis S. Collins, Nancy J. Cox, et al.David B. Goldstein, Lucia A. Hindorff, David J. Hunter, Mark I. McCarthy, Erin M. Ramos, Lon R. Cardon, Aravinda Chakravarti, Judy H. Cho, Alan E. Guttmacher, Augustine Kong, Leonid Kruglyak, Elaine Mardis, Charles N. Rotimi, Montgomery Slatkin, David Valle, Alice S. Whittemore, Michael Boehnke, Andrew G. Clark, Evan E. Eichler, Greg Gibson, Jonathan L. Haines, Trudy F. Mackay, Steven A. McCarroll, Peter M. Visscher posted to review human genome genetics disease bioinformatics by jclau on 2009-10-11 05:40:20 as along with 16 people and 1 group virolog timflutre daveGerrard leemachado lp2 natstreet ns6 balajis liqbbi josepe daforerog fenghezi rdiaz carolep merpublic djkt Journal picks
	A novel mutation of the CLCN1 gene associated with myotonia hereditaria in an Australian cattle dog. [My Copy] Journal of veterinary internal medicine / American College of Veterinary Internal Medicine, Vol. 21, No. 3. (n 2007), pp. 458-463. by Daniel F. Finnigan, Brad J. Hanna, Roberto Poma, Andrew J. Bendall posted to neuromuscular neurology myotonia model genetics clinical by jclau on 2009-09-29 19:01:33 as
	Disease signatures are robust across tissues and experiments [My Copy] Molecular Systems Biology, Vol. 5 (15 September 2009) by Joel T. Dudley, Robert Tibshirani, Tarangini Deshpande, Atul J. Butte posted to pathology microarray meta genetics genetic-test gene-expression gene disease-classification disease biomarker bioinformatics by jclau on 2009-09-19 15:32:57 as along with 14 people phoenixzxl tmmurali giovanni grahamc renatomilani ptrobajo zufar klo mingzhi ngehlenborg dswan winterschlaefer daforerog brianb
	A genome-wide association study identifies novel risk loci for type 2 diabetes. [My Copy] Nature, Vol. 445, No. 7130. (22 February 2007), pp. 881-885. by Robert Sladek, Ghislain Rocheleau, Johan Rung, et al.Christian Dina, Lishuang Shen, David Serre, Philippe Boutin, Daniel Vincent, Alexandre Belisle, Samy Hadjadj, Beverley Balkau, Barbara Heude, Guillaume Charpentier, Thomas J. Hudson, Alexandre Montpetit, Alexey V. Pshezhetsky, Marc Prentki, Barry I. Posner, David J. Balding, David Meyre, Constantin Polychronakos, Philippe Froguel posted to diabetes-type2 risk-factor genome genetics epidemiology diabetes bioinformatics by jclau on 2009-09-10 16:02:53 as along with 14 people wagrob liqbbi ptrobajo jbhiatt koller renewang jo_davies brant johncumbers msierk joepickrell sim82 dbgrant mcgannd
	TRANCE/RANKL knockout mice are protected from bone erosion in a serum transfer model of arthritis. [My Copy] The American journal of pathology, Vol. 159, No. 5. (November 2001), pp. 1689-1699. by A. R. Pettit, H. Ji, D. von Stechow, et al.R. Müller, S. R. Goldring, Y. Choi, C. Benoist, E. M. Gravallese posted to osteoporosis mouse knockout genetics bone arthritis by jclau on 2009-09-09 14:37:43 as
	The degenerate Y chromosome--can conversion save it? [My Copy] Reproduction, fertility, and development, Vol. 16, No. 5. (2004), pp. 527-534. by Jennifer Marshall A. Graves posted to review human genetics gender evolution by jclau on 2009-09-07 23:45:13 as along with 1 person usagi-kirin
	Evolution and Survival on Eutherian Sex Chromosomes [My Copy] PLoS Genet, Vol. 5, No. 7. (17 July 2009), e1000568. by Melissa A. Wilson, Kateryna D. Makova posted to monkey human genetics gender evolution bioinformatics by jclau on 2009-09-07 23:44:13 as along with 1 person djkt
	The prevalence of folate-remedial MTHFR enzyme variants in humans [My Copy] Proceedings of the National Academy of Sciences, Vol. 105, No. 23. (10 June 2008), pp. 8055-8060. by Nicholas J. Marini, Jennifer Gin, Janet Ziegle, et al.Kathryn H. Keho, David Ginzinger, Dennis A. Gilbert, Jasper Rine posted to vitamin prevalence phenotype pediatric mutation metabolic iem human genotype genetics epidemiology bioinformatics by jclau on 2009-08-26 14:44:40 as along with 1 person fpattyn
	Functional disconnectivity in subjects at high genetic risk of schizophrenia [My Copy] Brain, Vol. 128, No. 9. (September 2005), pp. 2097-2108. by Heather C. Whalley, Enrico Simonotto, Ian Marshall, et al.David G. Owens, Nigel H. Goddard, Eve C. Johnstone, Stephen M. Lawrie posted to genetics brain connectivity fmri functional human imaging schizophrenia by jclau on 2008-07-09 19:13:30 as along with 2 people prerona elv
	Identification of Genetically Mediated Cortical Networks: A Multivariate Study of Pediatric Twins and Siblings. [My Copy] Cereb Cortex (29 January 2008) by J E E. Schmitt, R K K. Lenroot, G L L. Wallace, et al.S Ordaz, K N N. Taylor, N Kabani, D Greenstein, J P P. Lerch, K S S. Kendler, M C C. Neale, J N N. Giedd posted to brain cortical-thickness genetics human imaging networks pediatric small-world twins by jclau on 2008-02-22 02:08:41 as
	Differences in genetic and environmental influences on the human cerebral cortex associated with development during childhood and adolescence. [My Copy] Hum Brain Mapp (27 November 2007) by Rhoshel K K. Lenroot, James E E. Schmitt, Sarah J J. Ordaz, et al.Gregory L L. Wallace, Michael C C. Neale, Jason P P. Lerch, Kenneth S S. Kendler, Alan C C. Evans, Jay N N. Giedd posted to genetics brain cerebral-cortex cortical-thickness development differences environmental imaging pediatric by jclau on 2008-02-22 02:07:43 as
	The emergence of HIV/AIDS in the Americas and beyond [My Copy] Proceedings of the National Academy of Sciences (1 November 2007), 0705329104. by Gilbert, Andrew Rambaut, Gabriela Wlasiuk, Thomas J. Spira, Arthur E. Pitchenik, Michael Worobey posted to aids emergence epidemiology genetics haiti hiv phylogenetics by jclau on 2007-11-06 19:10:12 as along with 2 people and 1 group trelew04 wsjames Oxford Virology
	Transgenerational response to nutrition, early life circumstances and longevity [My Copy] European Journal of Human Genetics, Vol. aop, No. current. by Gunnar Kaati, Lars O. Bygren, Marcus Pembrey, Michael Sjöström posted to genetics epigenetics longevity nutrition transgenerational by jclau on 2007-10-26 15:09:28 as
	Sex-specific, male-line transgenerational responses in humans [My Copy] European Journal of Human Genetics, Vol. aop, No. current. by Marcus E. Pembrey, Lars O. Bygren, Gunnar Kaati, et al.Sören Edvinsson, Kate Northstone, Michael Sjöström, Jean Golding, posted to epigenetics gender genetics human transgenerational by jclau on 2007-10-26 15:08:50 as along with 1 person epigenetics
	DNA methylation based testing of 450 patients suspected of having Prader-Willi syndrome. [My Copy] J Med Genet, Vol. 32, No. 2. (February 1995), pp. 88-92. by G. Gillessen-Kaesbach, S. Gross, S. Kaya-Westerloh, E. Passarge, B. Horsthemke posted to clinical dna genetics genetic-test methylation prader-willi by jclau on 2007-10-23 15:58:04 as
	Genetic analysis of the mammalian cell death machinery. [My Copy] Trends Genet, Vol. 18, No. 3. (March 2002), pp. 142-149. by N. Joza, G. Kroemer, J. M. Penninger posted to apoptosis cell genetics mammal review by jclau on 2007-10-12 15:23:44 as
	Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease. [My Copy] Nature, Vol. 375, No. 6534. (29 June 1995), pp. 754-760. by R. Sherrington, E. I. Rogaev, Y. Liang, et al.E. A. Rogaeva, G. Levesque, M. Ikeda, H. Chi, C. Lin, G. Li, K. Holman posted to alzheimers brain fad genetics mutation pathogenesis presenilin by jclau on 2007-08-21 16:55:08 as along with 2 people and 1 group daforerog jeremymiller GeschwindLab
	Candidate gene for the chromosome 1 familial Alzheimer's disease locus. [My Copy] Science, Vol. 269, No. 5226. (18 August 1995), pp. 973-977. by E. Levy-Lahad, W. Wasco, P. Poorkaj, et al.D. M. Romano, J. Oshima, W. H. Pettingell, C. E. Yu, P. D. Jondro, S. D. Schmidt, K. Wang posted to alzheimers brain fad genetics pathogenesis presenilin by jclau on 2007-08-21 16:54:02 as
	Increased amyloid-beta42(43) in brains of mice expressing mutant presenilin 1. [My Copy] Nature, Vol. 383, No. 6602. (24 October 1996), pp. 710-713. by K. Duff, C. Eckman, C. Zehr, et al.X. Yu, C. M. Prada, J. Perez-tur, M. Hutton, L. Buee, Y. Harigaya, D. Yager, D. Morgan, M. N. Gordon, L. Holcomb, L. Refolo, B. Zenk, J. Hardy, S. Younkin posted to genetics alzheimers amyloid app fad mutation plaque presenilin by jclau on 2007-04-24 22:15:13 as
	A pathogenic mutation for probable Alzheimer's disease in the APP gene at the N-terminus of beta-amyloid. [My Copy] Nat Genet, Vol. 1, No. 5. (August 1992), pp. 345-347. by M. Mullan, F. Crawford, K. Axelman, et al.H. Houlden, L. Lilius, B. Winblad, L. Lannfelt posted to genetics alzheimers app fad mutation by jclau on 2007-04-24 20:43:10 as
	Genetic linkage evidence for a familial Alzheimer's disease locus on chromosome 14 [My Copy] Science, Vol. 258, No. 5082. (23 October 1992), pp. 668-671. by Gd Schellenberg, Td Bird, Em Wijsman, et al.Ht Orr, L. Anderson, E. Nemens, Ja White, L. Bonnycastle, Jl Weber, Me Alonso, Al Et posted to genetics alzheimers fad mutation ps1 by jclau on 2007-04-24 20:41:02 as
	Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease. [My Copy] Nature, Vol. 349, No. 6311. (21 February 1991), pp. 704-706. by A. Goate, M. C. Chartier-Harlin, M. Mullan, et al.J. Brown, F. Crawford, L. Fidani, L. Giuffra, A. Haynes, N. Irving, L. James posted to genetics alzheimers app fad mutation by jclau on 2007-04-24 20:39:55 as along with 3 people vplagnol daforerog applebyb
	The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease. [My Copy] Nat Genet (14 January 2007) by Ekaterina Rogaeva, Yan Meng, Joseph H H. Lee, et al.Yongjun Gu, Toshitaka Kawarai, Fanggeng Zou, Taiichi Katayama, Clinton T T. Baldwin, Rong Cheng, Hiroshi Hasegawa, Fusheng Chen, Nobuto Shibata, Kathryn L L. Lunetta, Raphaelle Pardossi-Piquard, Christopher Bohm, Yosuke Wakutani, L Adrienne A. Cupples, Karen T T. Cuenco, Robert C C. Green, Lorenzo Pinessi, Innocenzo Rainero, Sandro Sorbi, Amalia Bruni, Ranjan Duara, Robert P P. Friedland, Rivka Inzelberg, Wolfgang Hampe, Hideaki Bujo, You-Qiang Q. Song, Olav M M. Andersen, Thomas E E. Willnow, Neill Graff-Radford, Ronald C C. Petersen, Dennis Dickson, Sandy D D. Der, Paul E E. Fraser, Gerold Schmitt-Ulms, Steven Younkin, Richard Mayeux, Lindsay A A. Farrer, Peter St George-Hyslop posted to alzheimers disease genetics receptor risk-factor sorl1 by jclau on 2007-03-20 22:12:54 as along with 2 people and 1 group kochhan giovanni GeschwindLab
	DNA microarray analysis of functionally discrete human brain regions reveals divergent transcriptional profiles. [My Copy] Neurobiol Dis, Vol. 14, No. 2. (November 2003), pp. 240-250. by S. J. Evans, P. V. Choudary, M. P. Vawter, et al.J. Li, J. H. Meador-Woodruff, J. F. Lopez, S. M. Burke, R. C. Thompson, R. M. Myers, E. G. Jones, W. E. Bunney, S. J. Watson, H. Akil posted to anatomy brain dna-microarray genetics by jclau on 2006-07-24 23:03:52 as along with 3 people and 1 group balicea jeremymiller jphekman GeschwindLab
	Controlling the false discovery rate in behavior genetics research. [My Copy] Behav Brain Res, Vol. 125, No. 1-2. (1 November 2001), pp. 279-284. by Y. Benjamini, D. Drai, G. Elmer, N. Kafkafi, I. Golani posted to fdr genetics by jclau on 2006-06-23 19:42:59 as along with 1 person Garamonfok
	Mapping heritability and molecular genetic associations with cortical features using probabilistic brain atlases: methods and applications to schizophrenia. [My Copy] Neuroinformatics, Vol. 4, No. 1. (2006), pp. 5-19. by T. D. Cannon, P. M. Thompson, T. G. van Erp, et al.M. Huttunen, J. Lonnqvist, J. Kaprio, A. W. Toga posted to atlas brain cerebral-cortex genetics human imaging mri by jclau on 2006-06-15 21:03:13 as along with 1 person decraene
	Genetics of brain structure and intelligence. [My Copy] Annu Rev Neurosci, Vol. 28 (2005), pp. 1-23. by A. W. Toga, P. M. Thompson posted to brain genetics imaging intelligence morphology by jclau on 2006-03-25 18:49:08 as along with 1 person timyu
	Optical projection tomography as a tool for 3D microscopy and gene expression studies. [My Copy] Science, Vol. 296, No. 5567. (19 April 2002), pp. 541-545. by J. Sharpe, U. Ahlgren, P. Perry, et al.B. Hill, A. Ross, J. Hecksher-Sørensen, R. Baldock, D. Davidson posted to gene-expression genetics imaging microscopy opt tomography by jclau on 2006-03-24 22:27:35 as along with 3 people and 1 group glyg GMTurner pick600 Computerized Tomography

Note: You may cite this page as: http://www.citeulike.org/user/jclau/tag/genetics

brain	498
imaging	453
human	300
mri	237
alzheimers	125
review	113
history	97
ultrasound	94
mouse	83
clinical	82
hom	80
morphometry	76
longitudinal	55
neurology	52
stroke	49
fmri	47
registration	46
statistics	46
dbm	45
pmoi	36
atlas	35
segmentation	33
transgenic	33
vbm	31
aging	30
genetics	30
intense	30
tissue-classification	30
epidemiology	29
volumetry	29
development	28
pediatric	28
automatic	25
pathology	25
connectivity	24
dnwhite	24
model	24
cerebral-cortex	23
disease	23
atrophy	22
neuroanatomy	22
classic	21
cortical-thickness	21
commentary	20
lesion	20
tbm	20
anatomy	19
clinical-trials	19
cortex	19
functional	19
dementia	18
neurosurgery	18
app	17
ct	17
skull	17
validation	17
automated	16
structural	16
textbook	16
hippocampus	15
ischemia	15
radiology	15
rehab	15
therapy	15
cancer	13
histology	13
multiple-sclerosis	13
neuroscience	13
phenotype	13
acute	12
comparison	12
cp	12
dti	12
immunohistochemistry	12
pd	12
stereotaxic	12
transcranial	12
classification	11
doppler	11
evaluation	11
multimodal	11
neurodegenerative	11
nonlinear	11
ps1	11
vascular	11
amyloid	10
cognitive	10
depression	10
mutation	10
networks	10
psych	10
behaviour	9
correlation	9
gene-expression	9
image-correction	9
motor	9
clustering	8
fad	8
family-medicine	8
intelligence	8
manual	8
nonparametric	8
probability-map	8
real-time	8
surgery	8
treatment	8
tumor	8
virology	8
anatomical	7
bioinformatics	7
cerebellum	7
gender	7
infection	7
mapping	7
microscopy	7
monkey	7
obsgyn	7
plasticity	7
rct	7
recovery	7
ventricles	7
cardiology	6
cell	6
deformable-model	6
eeg	6
hemorrhage	6
hifu	6
lacunar-infarct	6
mixed-effects	6
olfaction	6
pet	6
research-funding	6
roi	6
schizophrenia	6
social-media	6
aids	5
artefacts	5
asymmetry	5
average	5
bme	5
computation	5
deformation	5
dwi	5
function	5
hematology	5
hiv	5
immunology	5
infarction	5
mci	5
meta	5
mrs	5
neuromuscular	5
neuropathology	5
permutation	5
plaque	5
pneuro	5
power	5
presenilin	5
probabilistic-map	5
serial	5
simulation	5
small-world	5
surface	5
template	5
wm	5
alcoholism	4
antibiotics	4
antidepressant	4
biomarker	4
cerebrum	4
clinical-trial	4
cognition	4
csf	4
dbs	4
default-mode	4
downs-syndrome	4
elastic	4
elderly	4
emergency	4
epilepsy	4
gcs	4
gm	4
guidelines	4
hcv	4
healthcare	4
immunization	4
intellectual-disability	4
interventional-radiology	4
language	4
learning	4
memory	4
mixed-effect	4
mmse	4
morphology	4
mrm	4
myositis	4
neuron	4
parcellation	4
phantom	4
pipeline	4
post-mortem	4
preclinical	4
prevention	4
rat	4
reliability	4
shape	4
std	4
vr-space	4
academia	3
acquisition	3
adhd	3
apoptosis	3
autism	3
bootstrap	3
cadasil	3
chemotherapy	3
circle-of-willis	3
consciousness	3
contrast-agent	3
corpus-callosum	3
cytoarchitectonics	3
diabetes	3
differences	3
disease-classification	3
dopamine	3
drug	3
ekg	3
endoscopy	3
evolution	3
fdr	3
igns	3
leukoaraiosis	3
liver	3
memri	3
menopause	3
method	3
mmri	3
neurophysiology	3
normalization	3
pathogenesis	3
pregnancy	3
prevalence	3
psychiatry	3
pwi	3
qmri	3
random-field-theory	3
renal-failure	3
rft	3
risk-factor	3
sleep	3
statistical-mapping	3
suicide	3
synapse	3
talairach	3
tau-protein	3
thalamus	3
tomography	3
3d-mesh	2
activation	2
agreement	2
amygdala	2
analysis	2
art	2
bee	2
biography	2
bipolar	2
brian	2
bsi	2
cadaver	2
cardiovascular	2
cbf	2
charcot	2
classical	2
coexpression	2
comp-bio	2
critical-care	2
culture	2
data	2
dentate-gyrus	2
dfm	2
diet	2
dimorphism	2
dynamics	2
effective	2
entorhinal	2
environmental	2
epigenetics	2
evoked-potential	2
fetal	2
filtering	2
flair	2
ftd	2
ftld	2
gastro	2
gene	2
generalized	2
genetic-test	2
genome	2
genotype	2
gm-wm-density	2
hemiplegia	2
hypertension	2
hypothesis	2
icbm	2
ich	2
icu	2
influenza	2
in-vivo	2
jacobian	2
loc	2
medical-education	2
mi	2
mindfulness	2
mirtazapine	2
morphometrics	2
music	2
mutual-information	2
myopathy	2
neurite	2
neurochemistry	2
neurogenesis	2
nirs	2
nonuniformity	2
opinion	2
opt	2
optical	2
optimization	2
pag	2
pain	2
palliative-care	2
partial-volume-effect	2
pdapp	2
pe	2
perfusion	2
phenotyping	2
physics	2
physiology	2
pilot	2
placebo	2
population	2
postnatal	2
prediction	2
preterm	2
pre-term	2
prognosis	2
receptor-fingerprint	2
response-criteria	2
robotics	2
seizure	2
skull-stripping	2
social	2
subcortical	2
svm	2
t2	2
temporal-lobe	2
theory	2
thrombolysis	2
tractography	2
tract-tracing	2
transgenerational	2
ts65dn	2
twins	2
vaccination	2
vasculitis	2
vasculopathy	2
venous-drainage	2
white-matter	2
abdomen	1
accuracy	1
acoustic	1
adaptive	1
all	1
als	1
analgesia	1
anisotropic-filtering	1
apolipoprotein	1
apoptosome	1
applications	1
arthritis	1
arv	1
autoradiography	1
bias	1
birth	1
bland-altman	1
blockface	1
bone	1
breast	1
b-symptoms	1
case-study	1
cheatsheet	1
chemical	1
chemoprevention	1
chronic	1
cidp	1
claustrum	1
cochrane	1
compliance	1
concordance	1
connectome	1
continuity-of-care	1
convex-hulls	1
core	1
correction	1
cryoglobulinaemia	1
cystitis	1
dermatome	1
developmental-disability	1
diabetes-gest	1
diabetes-type1	1
diabetes-type2	1
disruption	1
distribution	1
dna	1
dna-microarray	1
downs	1
dyslexia	1
echocardiography	1
economics	1
embryo	1
emergence	1
endocrine	1
entropy	1
erp	1
errata	1
erratum	1
example	1
finance	1
fluid	1
fluoroscopy	1
fractional-volume	1
fragile-x	1
fse	1
fuzzy	1
gait	1
gal	1
galen	1
gbm	1
gbs	1
genetic-algorithm	1
geostatistics	1
gliosis	1
glitch	1
growth	1
gyral	1
gyrus	1
haiti	1
hardware	1
hba1c	1
headache	1
hirsutism	1
hmm	1
homeostasis	1
hpv	1
hydrocephalus	1
hyperostosis-frontalis-interna	1
ibm	1
id	1
iem	1
insomnia	1
insulin	1
interstitial-therapy	1
kidney	1
kinarm	1
knockout	1
lacuar-infarct	1
landmark	1
laplacian	1
laser	1
leukemia	1
lft	1
longevity	1
ltp	1
mammal	1
mass-preserving	1
maze	1
mca	1
mdd	1
meditation	1
meg	1
metabolic	1
methylation	1
microarray	1
mind	1
molecular-bio	1
morbidity	1
mortality	1
mrh	1
ms	1
multitasking	1
multivariate	1
muscle	1
mutant	1
mutual	1
myocardial	1
myotonia	1
narrative	1
neglect	1
neonatal	1
neuropathy	1
neuropsychology	1

jclau's genetics [30 articles] Export

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