Publication catalog

Biomedical publications with connected research

Browse 1,060,000 source-attributed publications. Article pages show available bibliographic context, indexed concepts and SPECTER2 related publications where supported by the source and graph. Missing metadata is not invented, and source retraction notices remain visible.

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Publications

Page 6432 of 10600

[Evoked potentials N200/P300 disorders and clinical phenotype in Cuban families with paranoid schizophrenia: a family-based association study].
Medwave | 2015-04-01 | PMID 25919584
Guerra López Seidel, Martín Reyes Migdyrai, Pedroso Rodríguez María de Los Ángeles and 6 more
Dynamic Metabolic Profiles and Tissue-Specific Source Effects on the Metabolome of Developing Seeds of Brassica napus.
PloS one | 2015-01-01 | PMID 25919591
Tan Helin, Xie Qingjun, Xiang Xiaoe and 5 more
Applying personal genetic data to injury risk assessment in athletes.
PloS one | 2014-01-01 | PMID 25919592
Goodlin Gabrielle T, Roos Andrew K, Roos Thomas R and 4 more
A Complete Pathway Model for Lipid A Biosynthesis in Escherichia coli.
PloS one | 2014-01-01 | PMID 25919634
Emiola Akintunde, George John, Andrews Steven S
Apolipoprotein E genotype modulates effects of vitamin B12 and homocysteine on grey matter volume in Alzheimer's disease.
Psychogeriatrics : the official journal of the Japanese Psychogeriatric Society | 2016-01-01 | PMID 25919635
Lee Young-Min, Ha Ji-Kyung, Park Je-Min and 8 more
Genes: APOE
Hepatitis E Virus and Related Viruses in Animals.
Transboundary and emerging diseases | 2017-02-01 | PMID 25919649
Thiry D, Mauroy A, Pavio N and 4 more
MicroRNA-224 is associated with colorectal cancer progression and response to 5-fluorouracil-based chemotherapy by KRAS-dependent and -independent mechanisms.
British journal of cancer | 2015-04-28 | PMID 25919696
Amankwatia E B, Chakravarty P, Carey F A and 5 more
Genes: KRAS, BRAF
Cardiolipin remodeling by TAZ/tafazzin is selectively required for the initiation of mitophagy.
Autophagy | 2015-04-03 | PMID 25919711
Hsu Paul, Liu Xiaolei, Zhang Jun and 3 more
Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers.
Breast cancer research : BCR | 2014-12-31 | PMID 25919761
Kuchenbaecker Karoline B, Neuhausen Susan L, Robson Mark and 202 more
Genes: BRCA1, BRCA2
Hidden diversity in the freshwater planktonic diatom Asterionella formosa.
Molecular ecology | 2015-06-01 | PMID 25919789
Van den Wyngaert S, Möst M, Freimann R and 2 more
Associations between CLCNKA_B tag SNPs with essential hypertension and interactions between genetic and environmental factors in an island population in China.
Clinical and experimental hypertension (New York, N.Y. : 1993) | 2015-01-01 | PMID 25919862
Chen Xin, Zhou Bo, Hou Xiaowen and 5 more
Genes: CLCNKA
[Molecular bases of α-thalassemia in Argentina].
Medicina | 2015-01-01 | PMID 25919868
Scheps Karen G, Francipane Liliana, Nash Abigail and 3 more
Genes: CAMP
Genetic Diversity and Drug Resistance Among Antiretroviral Treatment-Failed Individuals from 2010 to 2012 in Honghe, China.
AIDS research and human retroviruses | 2015-08-01 | PMID 25919896
Yang Cuixian, Yang Shaomin, Li Jianjian and 4 more
Applying ecological models to communities of genetic elements: the case of neutral theory.
Molecular ecology | 2015-07-01 | PMID 25919906
Linquist Stefan, Cottenie Karl, Elliott Tyler A and 3 more
A common variant in the MTNR1b gene is associated with increased risk of impaired fasting glucose (IFG) in youth with obesity.
Obesity (Silver Spring, Md.) | 2015-05-01 | PMID 25919927
Zheng Chao, Dalla Man Chiara, Cobelli Claudio and 8 more
Whole genome comparison of a large collection of mycobacteriophages reveals a continuum of phage genetic diversity.
eLife | 2015-04-28 | PMID 25919952
Pope Welkin H, Bowman Charles A, Russell Daniel A and 7 more
BRAF-mutated carcinomas among thyroid nodules with prior indeterminate FNA report: a systematic review and meta-analysis.
Clinical endocrinology | 2016-03-01 | PMID 25920006
Trimboli Pierpaolo, Treglia Giorgio, Condorelli Emma and 4 more
Genes: BRAF
Impact of climate change on cold hardiness of Douglas-fir (Pseudotsuga menziesii): environmental and genetic considerations.
Global change biology | 2015-10-01 | PMID 25920066
Bansal Sheel, St Clair J Bradley, Harrington Constance A and 1 more
Genetics of liver disease: From pathophysiology to clinical practice.
Journal of hepatology | 2015-04-01 | PMID 25920091
Karlsen Tom H, Lammert Frank, Thompson Richard J
Identifying areas and risk groups with localised Mycobacterium tuberculosis transmission in northern England from 2010 to 2012: spatiotemporal analysis incorporating highly discriminatory genotyping data.
Thorax | 2016-08-01 | PMID 25920328
Saavedra-Campos María, Welfare William, Cleary Paul and 6 more
Neoadjuvant chemotherapy in locally advanced colon cancer. A phase II trial.
Acta oncologica (Stockholm, Sweden) | 2015-11-01 | PMID 25920359
Jakobsen Anders, Andersen Fahimeh, Fischer Anders and 7 more
Genes: BRAF, KRAS
Prevalence of founder mutations in the BRCA1 and BRCA2 genes among unaffected women from the Bahamas.
Clinical genetics | 2016-03-01 | PMID 25920394
Trottier M, Lunn J, Butler R and 12 more
Genes: BRCA1, BRCA2
Correlation of C/EBPα expression with response and resistance to imatinib in chronic myeloid leukaemia.
Japanese journal of clinical oncology | 2015-08-01 | PMID 25920395
Kagita Sailaja, Uppalapati Srihari, Gundeti Sadasivudu and 1 more
Genes: BCR
Mutations in the RAS and PI3K pathways are associated with metastatic location in colorectal cancers.
Journal of surgical oncology | 2015-06-01 | PMID 25920435
Lan Yuan-Tzu, Jen-Kou Lin, Lin Chien-Hsing and 7 more
Genes: EGFR, NRAS, PTEN
2015 Guidelines for Establishing Genetically Modified Rat Models for Cardiovascular Research.
Journal of cardiovascular translational research | 2015-06-01 | PMID 25920443
Flister Michael J, Prokop Jeremy W, Lazar Jozef and 3 more
Single nucleotide polymorphism of toll-like receptor 4 (TLR4) is associated with juvenile spondyloarthritis in Croatian population.
Clinical rheumatology | 2015-12-01 | PMID 25920454
Perica Marija, Vidović Mandica, Lamot Lovro and 5 more
Genes: TLR4, NLRP3, TLR2
A rural worker infected with a bovine-prevalent genotype of Campylobacter fetus subsp. fetus supports zoonotic transmission and inconsistency of MLST and whole-genome typing.
European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology | 2015-08-01 | PMID 25920493
Iraola G, Betancor L, Calleros L and 6 more
Population growth rate and genetic variability of small and large populations of Red flour beetle (Tribolium castaneum) following multigenerational exposure to copper.
Ecotoxicology (London, England) | 2015-07-01 | PMID 25920509
Laskowski Ryszard, Radwan Jacek, Kuduk Katarzyna and 2 more
Role of heteroplasmic mutations in the mitochondrial genome and the ID4 gene promoter methylation region in the pathogenesis of chronic aplastic anemia in patients suffering from Kidney yin deficiency.
Chinese journal of integrative medicine | 2016-06-01 | PMID 25920536
Cui Xing, Wang Jing-Yi, Liu Kui and 4 more
Lipids, obesity and gallbladder disease in women: insights from genetic studies using the cardiovascular gene-centric 50K SNP array.
European journal of human genetics : EJHG | 2016-01-01 | PMID 25920552
Rodriguez Santiago, Gaunt Tom R, Guo Yiran and 20 more
Genes: ABCG5, ABCG8, GCKR
Common polygenic variation in coeliac disease and confirmation of ZNF335 and NIFA as disease susceptibility loci.
European journal of human genetics : EJHG | 2016-02-01 | PMID 25920553
Coleman Ciara, Quinn Emma M, Ryan Anthony W and 17 more
LRP5 variants may contribute to ADPKD.
European journal of human genetics : EJHG | 2016-02-01 | PMID 25920554
Cnossen Wybrich R, te Morsche René H M, Hoischen Alexander and 9 more
Genes: LRP5, PKD1, PKD2
Joubert syndrome: genotyping a Northern European patient cohort.
European journal of human genetics : EJHG | 2016-02-01 | PMID 25920555
Kroes Hester Y, Monroe Glen R, van der Zwaag Bert and 9 more
Genes: AHI1, TMEM67
Ten new cases further delineate the syndromic intellectual disability phenotype caused by mutations in DYRK1A.
European journal of human genetics : EJHG | 2015-11-01 | PMID 25920557
Bronicki Lucas M, Redin Claire, Drunat Severine and 18 more
Epidemiological, clinical and biochemical characterization of the p.(Ala359Asp) SMPD1 variant causing Niemann-Pick disease type B.
European journal of human genetics : EJHG | 2016-02-01 | PMID 25920558
Acuña Mariana, Martínez Pablo, Moraga Carol and 11 more
Genes: SMPD1
The application of single strand conformation polymorphism (SSCP) analysis in determining Hepatitis E virus intra-host diversity.
Journal of virological methods | 2015-09-01 | PMID 25920567
Černi S, Prpić J, Jemeršić L and 1 more
Genome-wide QTL mapping of saltwater tolerance in sibling species of Anopheles (malaria vector) mosquitoes.
Heredity | 2015-11-01 | PMID 25920668
Smith H A, White B J, Kundert P and 4 more
Short-term genetic consequences of habitat loss and fragmentation for the neotropical palm Oenocarpus bataua.
Heredity | 2015-11-01 | PMID 25920669
Browne L, Ottewell K, Karubian J
Quantifying heritable variation in fitness-related traits of wild, farmed and hybrid Atlantic salmon families in a wild river environment.
Heredity | 2015-08-01 | PMID 25920670
Reed T E, Prodöhl P, Hynes R and 3 more
Vicariance and marine migration in continental island populations of a frog endemic to the Atlantic Coastal forest.
Heredity | 2015-09-01 | PMID 25920672
Duryea M C, Zamudio K R, Brasileiro C A
Targeted disruption of organic cation transporter 3 attenuates the pharmacologic response to metformin.
Molecular pharmacology | 2015-07-01 | PMID 25920679
Chen Eugene C, Liang Xiaomin, Yee Sook Wah and 4 more
The associations of 25-hydroxyvitamin D levels, vitamin D binding protein gene polymorphisms, and race with risk of incident fracture-related hospitalization: Twenty-year follow-up in a bi-ethnic cohort (the ARIC Study).
Bone | 2015-09-01 | PMID 25920689
Takiar Radhika, Lutsey Pamela L, Zhao Di and 6 more
Genes: DBP
Genetic and functional studies reveal a novel noncoding variant in GALT associated with a false positive newborn screening result for galactosemia.
Clinica chimica acta; international journal of clinical chemistry | 2015-06-15 | PMID 25920691
Liu Ying, Sidhu Alpa, Bean Lora H and 2 more
Genes: GALT
High functioning male with fragile X syndrome and fragile X-associated tremor/ataxia syndrome.
American journal of medical genetics. Part A | 2015-09-01 | PMID 25920745
Basuta Kirin, Schneider Andrea, Gane Louise and 5 more
Genes: FMR1
Baseline prevalence and emergence of protease inhibitor resistance mutations following treatment in chronic HCV genotype-1-infected individuals.
Antiviral therapy | 2015-01-01 | PMID 25920764
Nguyen Linh Thuy, Gray Emma, Dean Jonathan and 8 more
Genes: BOC
Visceral abdominal fat accumulation predicts the conversion of metabolically healthy obese subjects to an unhealthy phenotype.
International journal of obesity (2005) | 2015-09-01 | PMID 25920773
Hwang Y-C, Hayashi T, Fujimoto W Y and 4 more
Cross-sectional population associations between detailed adiposity measures and C-reactive protein levels at age 6 years: the Generation R Study.
International journal of obesity (2005) | 2015-07-01 | PMID 25920775
Toemen L, Gishti O, Vogelezang S and 5 more
Genetic variants within the serotonin transporter associated with familial risk for major depression.
Psychiatry research | 2015-07-30 | PMID 25920807
Talati Ardesheer, Guffanti Guia, Odgerel Zagaa and 7 more
The phenotype of multiple congenital anomalies-hypotonia-seizures syndrome 1: report and review.
American journal of medical genetics. Part A | 2015-09-01 | PMID 25920937
Couser Natario L, Masood Maheer M, Strande Natasha T and 9 more
Genes: PIGN
Pattern of SMARCB1 (INI1) and SMARCA4 (BRG1) in poorly differentiated endometrioid adenocarcinoma of the uterus: analysis of a series with emphasis on a novel SMARCA4-deficient dedifferentiated rhabdoid variant.
Annals of diagnostic pathology | 2015-08-01 | PMID 25920939
Strehl Johanna D, Wachter David L, Fiedler Jutta and 4 more
Genes: SMARCA4, SMARCB1
Chromosomal microarray in unexplained severe early onset epilepsy - A single centre cohort.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society | 2015-07-01 | PMID 25920948
Allen Nicholas M, Conroy Judith, Shahwan Amre and 4 more
APOE ɛ2 is associated with white matter hyperintensity volume in CADASIL.
Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism | 2016-01-01 | PMID 25920955
Gesierich Benno, Opherk Christian, Rosand Jonathan and 24 more
Genes: APOE
20-HETE is associated with unfavorable outcomes in subarachnoid hemorrhage patients.
Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism | 2015-09-01 | PMID 25920956
Donnelly Mark K, Crago Elizabeth A, Conley Yvette P and 6 more
Integrating chemical mutagenesis and whole-genome sequencing as a platform for forward and reverse genetic analysis of Chlamydia.
Cell host & microbe | 2015-05-13 | PMID 25920978
Kokes Marcela, Dunn Joe Dan, Granek Joshua A and 4 more
High-dose erlotinib for refractory leptomeningeal metastases after failure of standard-dose EGFR-TKIs.
Cancer chemotherapy and pharmacology | 2015-06-01 | PMID 25921002
Kawamura Takahisa, Hata Akito, Takeshita Jumpei and 4 more
Genes: EGFR
Enrichment for Northern European-derived multiple sclerosis risk alleles in Sardinia.
Multiple sclerosis (Houndmills, Basingstoke, England) | 2015-10-01 | PMID 25921054
Hadjixenofontos A, Gourraud P A, Bakthavachalam V and 6 more
Clinical management of patients with ASXL1 mutations and Bohring-Opitz syndrome, emphasizing the need for Wilms tumor surveillance.
American journal of medical genetics. Part A | 2015-09-01 | PMID 25921057
Russell Bianca, Johnston Jennifer J, Biesecker Leslie G and 12 more
Genes: ASXL1
Human chromosome segregation involves multi-layered regulation of separase by the peptidyl-prolyl-isomerase Pin1.
Molecular cell | 2015-05-07 | PMID 25921067
Hellmuth Susanne, Rata Scott, Brown Andreas and 3 more
Clinical features of bilateral temporal bone xanthoma with LDLR gene mutation.
International journal of pediatric otorhinolaryngology | 2015-07-01 | PMID 25921077
Han Yu, Gao Wei, Liang Pengfei and 3 more
Genes: LDLR
Allele and Genotype Frequencies of the Polymorphic Methylenetetrahydrofolate Reductase and Lung Cancer in ther Jordanian Population: a Case Control Study.
Asian Pacific journal of cancer prevention : APJCP | 2015-01-01 | PMID 25921104
Al-Motassem Yousef, Shomaf Maha, Said Ismail and 5 more
Genes: MTHFR
Association Study of Single-Nucleotide Polymorphisms of STAT2/STAT3/IFN-γ Genes in Cervical Cancer in Southern Chinese Han Women.
Asian Pacific journal of cancer prevention : APJCP | 2015-01-01 | PMID 25921106
Yuan Yuan, Fan Jie-Lin, Yao Fang-Ling and 4 more
Genes: STAT2, STAT3
Pro-(IL-18) and Anti-(IL-10) Inflammatory Promoter Genetic Variants (Intrinsic Factors) with Tobacco Exposure (Extrinsic Factors) May Influence Susceptibility and Severity of Prostate Carcinoma: A Prospective Study.
Asian Pacific journal of cancer prevention : APJCP | 2015-01-01 | PMID 25921117
Dwivedi Shailendra, Singh Sarvesh, Goel Apul and 5 more
CYP2C19 Genotype Could be a Predictive Factor for Aggressive Manifestations of Hepatocellular Carcinoma Related with Chronic Hepatitis B Infection in Thailand.
Asian Pacific journal of cancer prevention : APJCP | 2015-01-01 | PMID 25921128
Nun-Anan Pongjarat, Chonprasertsuk Soonthorn, Siramolpiwat Sith and 4 more
Association of XRCC1 Arg399Gln Polymorphism with Colorectal Cancer Risk: A HuGE Meta Analysis of 35 Studies.
Asian Pacific journal of cancer prevention : APJCP | 2015-01-01 | PMID 25921133
Forat-Yazdi Mohammad, Gholi-Nataj Mohsen, Neamatzadeh Hossein and 2 more
Genes: XRCC1
Stromal modulation and its role in the diagnosis of papillary patterned thyroid lesions.
Asian Pacific journal of cancer prevention : APJCP | 2015-01-01 | PMID 25921136
Daoud Sahar Aly, Esmail Reham Shehab El Nemr, Hareedy Amal Ahmed and 1 more
Single nucleotide polymorphisms in the Gc gene for vitamin D binding protein in common cancers in Thailand.
Asian Pacific journal of cancer prevention : APJCP | 2015-01-01 | PMID 25921141
Maneechay Wanwisa, Boonpipattanapong Teeranut, Kanngurn Samornmas and 3 more
Expression Profile Analysis of Zinc Transporters (ZIP4, ZIP9, ZIP11, ZnT9) in Gliomas and their Correlation with IDH1 Mutation Status.
Asian Pacific journal of cancer prevention : APJCP | 2015-01-01 | PMID 25921144
Kang Xing, Chen Rong, Zhang Jie and 4 more
Genes: IDH1
TP53 Codon 72 Polymorphisms and Lung Cancer Risk in the Bangladeshi Population.
Asian Pacific journal of cancer prevention : APJCP | 2015-01-01 | PMID 25921167
Chowdhury Miraj Kobad, Moniruzzaman Md, Emran Abdullah Al and 3 more
High Frequency of Codon 12 but not Codon 13 and 61 K-ras Gene Mutations in Invasive Ductal Carcinoma of Breast in a South Indian Population.
Asian Pacific journal of cancer prevention : APJCP | 2015-01-01 | PMID 25921169
Sushma C, Prasad Shiva, Devi Rudrama and 3 more
Promyelocytic Leukemia (PML) Gene Mutations may not Contribute to Gastric Adenocarcinoma Development.
Asian Pacific journal of cancer prevention : APJCP | 2015-01-01 | PMID 25921172
Imani-Saber Zeinab, Yousefi-Razin Ehsan, Javaheri Mona and 3 more
Genes: PML
Breast Cancer Association with CYP1A2 Activity and Gene Polymorphisms--a Preliminary Case-control Study in Tunisia.
Asian Pacific journal of cancer prevention : APJCP | 2015-01-01 | PMID 25921178
Imene Ayari, Maurice Arnaud J, Arij Mani and 2 more
A Novel KCNJ13 Nonsense Mutation and Loss of Kir7.1 Channel Function Causes Leber Congenital Amaurosis (LCA16).
Human mutation | 2015-07-01 | PMID 25921210
Pattnaik Bikash R, Shahi Pawan K, Marino Meghan J and 6 more
Genes: KCNJ13, RPE
Common genetic variants in epigenetic machinery genes and risk of upper gastrointestinal cancers.
International journal of epidemiology | 2015-08-01 | PMID 25921222
Sung Hyuna, Yang Howard H, Zhang Han and 22 more
Genes: GCA, DICER1, EED
Exome sequencing of patients with histiocytoid cardiomyopathy reveals a de novo NDUFB11 mutation that plays a role in the pathogenesis of histiocytoid cardiomyopathy.
American journal of medical genetics. Part A | 2015-09-01 | PMID 25921236
Shehata Bahig M, Cundiff Caitlin A, Lee Kevin and 7 more
Genes: NDUFB11, NDUFAF2, NDUFB9
ABCB1 polymorphisms correlate with susceptibility to adult acute leukemia and response to high-dose methotrexate.
Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine | 2015-09-01 | PMID 25921280
Ma Chuan-Xiang, Sun Yong-Hong, Wang Hai-Ying
Genes: ABCB1
Association between genetic variants in SLC25A12 and risk of autism spectrum disorders: An integrated meta-analysis.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics | 2015-06-01 | PMID 25921325
Liu Jun, Yang Aiping, Zhang Qunwei and 8 more
Progressive influence of body mass index-associated genetic markers in rural Gambians.
Journal of medical genetics | 2015-06-01 | PMID 25921383
Fulford Anthony J, Ong Ken K, Elks Cathy E and 2 more
Oncostatin M protects against demyelination by inducing a protective microglial phenotype.
Glia | 2015-10-01 | PMID 25921393
Janssens Kris, Maheshwari Anurag, Van den Haute Chris and 5 more
Genes: OSM, OSMR
Rare de novo deletion of metabotropic glutamate receptor 7 (GRM7) gene in a patient with autism spectrum disorder.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics | 2015-06-01 | PMID 25921429
Liu Yi, Zhang Yanqing, Zhao Dongmei and 6 more
Genes: GRM7
Proteomic analysis of reproduction proteins involved in litter size from porcine placenta.
Bioscience, biotechnology, and biochemistry | 2015-01-01 | PMID 25921448
Lee Dong-Gi, Nam Juhyun, Kim Sam Woong and 4 more
Genes: RBP4
Molecular identification of rare FY*Null and FY*X alleles in Caucasian thalassemic family from Sardinia.
Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis | 2015-10-01 | PMID 25921504
Manfroi Silvia, Scarcello Antonio, Pagliaro Pasqualepaolo
Characterization of MDR and XDR Streptococcus pneumoniae in Canada, 2007-13.
The Journal of antimicrobial chemotherapy | 2015-08-01 | PMID 25921512
Golden Alyssa R, Rosenthal Margot, Fultz Ben and 7 more
ZNF804A rs1344706 is associated with cortical thickness, surface area, and cortical volume of the unmedicated first episode schizophrenia and healthy controls.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics | 2015-06-01 | PMID 25921517
Wei Qinling, Li Meng, Kang Zhuang and 9 more
A systems approach identifies networks and genes linking sleep and stress: implications for neuropsychiatric disorders.
Cell reports | 2015-05-05 | PMID 25921536
Jiang Peng, Scarpa Joseph R, Fitzpatrick Karrie and 10 more
Innate and adaptive immune functions of peyer's patch monocyte-derived cells.
Cell reports | 2015-05-05 | PMID 25921539
Bonnardel Johnny, Da Silva Clément, Henri Sandrine and 5 more
Genes: TLR7, TNF
Cholangiocyte senescence caused by lysophosphatidylcholine as a potential implication in carcinogenesis.
Journal of hepato-biliary-pancreatic sciences | 2015-09-01 | PMID 25921542
Shimizu Rina, Kanno Keishi, Sugiyama Akiko and 8 more
Genes: MUTYH, OGG1
Associations between polymorphisms in the SYK promoter and susceptibility to sporadic colorectal cancer in a Southern Han Chinese population - a short report.
Cellular oncology (Dordrecht, Netherlands) | 2015-04-01 | PMID 25921550
Peng Hui, Huang Jun, Hu Ying and 5 more
Genes: SYK
Analysis of the Reasons for Non-Uptake of Predictive Testing for Huntington's Disease in Spain: A Qualitative Study.
Journal of genetic counseling | 2015-12-01 | PMID 25921556
Rivera-Navarro Jesús, Cubo Esther, Mariscal Natividad
Traditional vs. genetic pathogenesis of arrhythmogenic right ventricular cardiomyopathy.
Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology | 2015-12-01 | PMID 25921558
Que Dongdong, Yang Pingzhen, Song Xudong and 1 more
An angiotensin-converting enzyme (ACE) polymorphism may mitigate the effects of angiotensin-pathway medications on posttraumatic stress symptoms.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics | 2015-06-01 | PMID 25921615
Nylocks K M, Michopoulos V, Rothbaum A O and 9 more
Genes: ACE
Identification of a gene controlling variation in the salt tolerance of rapeseed (Brassica napus L.).
Planta | 2015-07-01 | PMID 25921693
Yong Hui-Yee, Wang Chunlei, Bancroft Ian and 4 more
The impact of genome wide supported microRNA-137 (MIR137) risk variants on frontal and striatal white matter integrity, neurocognitive functioning, and negative symptoms in schizophrenia.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics | 2015-07-01 | PMID 25921703
Kuswanto Carissa Nadia, Sum Min Yi, Qiu Anqi and 3 more
APOL1 Genotype and Glomerular and Tubular Kidney Injury in Women With HIV.
American journal of kidney diseases : the official journal of the National Kidney Foundation | 2015-06-01 | PMID 25921719
Jotwani Vasantha, Shlipak Michael G, Scherzer Rebecca and 10 more
Genes: APOL1, ACR
The effect of mild traumatic brain injury on peripheral nervous system pathology in wild-type mice and the G93A mutant mouse model of motor neuron disease.
Neuroscience | 2015-07-09 | PMID 25921732
Evans T M, Jaramillo C A, Sataranatarajan K and 4 more
Array-comparative genomic hybridization analysis of a cohort of Saudi patients with epilepsy.
CNS & neurological disorders drug targets | 2015-01-01 | PMID 25921748
Faheem Muhammad, Naseer Muhammad I, Chaudhary Adeel G and 6 more
Genes: CHRNA4, GABRG3, KCNQ2, NRXN3, PPDPF
rs2043211 polymorphism in CARD8 is not associated with Tourette syndrome in a family-based association study in the Chinese Han population.
International journal of psychiatry in medicine | 2015-01-01 | PMID 25921775
Yi Mingji, Shao Xiaohui, Ma Jianhua and 3 more
Genes: CARD8
Diagnostic stability in young children at risk for autism spectrum disorder: a baby siblings research consortium study.
Journal of child psychology and psychiatry, and allied disciplines | 2015-09-01 | PMID 25921776
Ozonoff Sally, Young Gregory S, Landa Rebecca J and 9 more
Eye color: A potential indicator of alcohol dependence risk in European Americans.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics | 2015-07-01 | PMID 25921801
Sulovari Arvis, Kranzler Henry R, Farrer Lindsay A and 2 more
Genes: GABRB3, GABRG3, GRM5, HERC2, OCA2, TYR
Hyposmia correlates with SNCA variant and non-motor symptoms in Chinese patients with Parkinson's disease.
Parkinsonism & related disorders | 2015-06-01 | PMID 25921825
Chen Wei, Kang Wen-Yan, Chen Shuai and 5 more
Genes: SNCA
Evidence for negative selection of gene variants that increase dependence on dietary choline in a Gambian cohort.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology | 2015-08-01 | PMID 25921832
Silver Matt J, Corbin Karen D, Hellenthal Garrett and 7 more
Genes: CHDH, MTHFD1, PEMT