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 7916 of 10600

Interaction specificity of clustered protocadherins inferred from sequence covariation and structural analysis.
Proceedings of the National Academy of Sciences of the United States of America | 2019-09-03 | PMID 31431536
Nicoludis John M, Green Anna G, Walujkar Sanket and 4 more
Mitochondrial DNA variation modulates alveolar development in newborn mice exposed to hyperoxia.
American journal of physiology. Lung cellular and molecular physiology | 2019-12-01 | PMID 31432715
Kandasamy Jegen, Rezonzew Gabriel, Jilling Tamas and 2 more
Targeting Autophagy in Cancer: Recent Advances and Future Directions.
Cancer discovery | 2019-09-01 | PMID 31434711
Amaravadi Ravi K, Kimmelman Alec C, Debnath Jayanta
Genetic variants in glutamine metabolic pathway genes predict cutaneous melanoma-specific survival.
Molecular carcinogenesis | 2019-11-01 | PMID 31435991
Chen Ka, Liu Hongliang, Liu Zhensheng and 6 more
Genes: HAL, LGSN, NOXRED1
Behavioral predictors of autism recurrence are genetically independent and influence social reciprocity: evidence that polygenic ASD risk is mediated by separable elements of developmental liability.
Translational psychiatry | 2019-08-22 | PMID 31439834
Pohl Alexa, Jones Warren R, Marrus Natasha and 3 more
Differential associations of allergic disease genetic variants with developmental profiles of eczema, wheeze and rhinitis.
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology | 2019-11-01 | PMID 31441980
Clark Hannah, Granell Raquel, Curtin John A and 6 more
Genes: FLG, GSDMB
Detecting time-evolving phenotypic topics via tensor factorization on electronic health records: Cardiovascular disease case study.
Journal of biomedical informatics | 2019-10-01 | PMID 31445983
Zhao Juan, Zhang Yun, Schlueter David J and 7 more
Case Report: Investigation and molecular genetic diagnosis of familial hypomagnesaemia.
F1000Research | 2019-01-01 | PMID 31448104
Willows Jamie, Al Badi Maryam, Richardson Chloe and 4 more
Protective HLA alleles are associated with reduced LPS levels in acute HIV infection with implications for immune activation and pathogenesis.
PLoS pathogens | 2019-08-01 | PMID 31449552
Claiborne Daniel T, Scully Eileen P, Palmer Christine D and 15 more
Genes: CD4
Mapping person-to-person variation in viral mutations that escape polyclonal serum targeting influenza hemagglutinin.
eLife | 2019-08-27 | PMID 31452511
Lee Juhye M, Eguia Rachel, Zost Seth J and 9 more
Spontaneous mutations of the Zpld1 gene in mice cause semicircular canal dysfunction but do not impair gravity receptor or hearing functions.
Scientific reports | 2019-08-27 | PMID 31455802
Vijayakumar Sarath, Jones Sherri M, Jones Timothy A and 2 more
Genes: ZPLD1, ABR
Long-term isolation at a low effective population size greatly reduced genetic diversity in Gulf of California fin whales.
Scientific reports | 2019-08-27 | PMID 31455830
Rivera-León Vania E, Urbán Jorge, Mizroch Sally and 5 more
The TMEM106B FTLD-protective variant, rs1990621, is also associated with increased neuronal proportion.
Acta neuropathologica | 2020-01-01 | PMID 31456032
Li Zeran, Farias Fabiana H G, Dube Umber and 21 more
Genes: TMEM106B
A unified encyclopedia of human functional DNA elements through fully automated annotation of 164 human cell types.
Genome biology | 2019-08-28 | PMID 31462275
Libbrecht Maxwell W, Rodriguez Oscar L, Weng Zhiping and 3 more
Best practices for bioinformatic characterization of neoantigens for clinical utility.
Genome medicine | 2019-08-28 | PMID 31462330
Richters Megan M, Xia Huiming, Campbell Katie M and 3 more
Elevated risk of invasive group A streptococcal disease and host genetic variation in the human leucocyte antigen locus.
Genes and immunity | 2020-01-01 | PMID 31462703
Parks Tom, Elliott Katherine, Lamagni Theresa and 14 more
An anti-CRF antibody suppresses the HPA axis and reverses stress-induced phenotypes.
The Journal of experimental medicine | 2019-11-04 | PMID 31467037
Futch Hunter S, McFarland Karen N, Moore Brenda D and 19 more
Transcriptional profiling of corneal stromal cells derived from patients with keratoconus.
Scientific reports | 2019-08-29 | PMID 31467338
Sharif Rabab, Khaled Mariam L, McKay Tina B and 2 more
Genes: EGFR, HIF1A, HSPB1, LGALS3BP, MME, NEDD4, SDC2, SNTA1
Assessment of network module identification across complex diseases.
Nature methods | 2019-09-01 | PMID 31471613
Choobdar Sarvenaz, Ahsen Mehmet E, Crawford Jake and 19 more
Oral HPV prevalence and HPV vaccination among special needs population in the US.
Papillomavirus research (Amsterdam, Netherlands) | 2019-12-01 | PMID 31473308
Chandrupatla Siddardha G, Khalid Isma, Tavares Mary
Allele-specific expression and high-throughput reporter assay reveal functional genetic variants associated with alcohol use disorders.
Molecular psychiatry | 2021-04-01 | PMID 31477794
Rao Xi, Thapa Kriti S, Chen Andy B and 18 more
mRNA structure determines modification by pseudouridine synthase 1.
Nature chemical biology | 2019-10-01 | PMID 31477916
Carlile Thomas M, Martinez Nicole M, Schaening Cassandra and 4 more
Ultrarare variants drive substantial cis heritability of human gene expression.
Nature genetics | 2019-09-01 | PMID 31477931
Hernandez Ryan D, Uricchio Lawrence H, Hartman Kevin and 3 more
Orally Bioavailable Androgen Receptor Degrader, Potential Next-Generation Therapeutic for Enzalutamide-Resistant Prostate Cancer.
Clinical cancer research : an official journal of the American Association for Cancer Research | 2019-11-15 | PMID 31481513
Ponnusamy Suriyan, He Yali, Hwang Dong-Jin and 12 more
Genes: AR
The uptake of family screening in hypertrophic cardiomyopathy and an online video intervention to facilitate family communication.
Molecular genetics & genomic medicine | 2019-11-01 | PMID 31482667
Harris Stephanie, Cirino Allison L, Carr Christina W and 13 more
Whole-exome sequencing in familial keratoconus: the challenges of a genetically complex disorder.
Arquivos brasileiros de oftalmologia | 2019-01-01 | PMID 31482965
Magalhães Otávio de Azevedo, Kowalski Thayne Woycinck, Wachholz Gabriela Elis and 1 more
Genes: ZNF469
Residual apoptotic activity of a tumorigenic p53 mutant improves cancer therapy responses.
The EMBO journal | 2019-10-15 | PMID 31483066
Timofeev Oleg, Klimovich Boris, Schneikert Jean and 13 more
Genetic hallmarks of recurrent/metastatic adenoid cystic carcinoma.
The Journal of clinical investigation | 2019-10-01 | PMID 31483290
Ho Allen S, Ochoa Angelica, Jayakumaran Gowtham and 26 more
Genes: MYB, NOTCH1, ARID1B, KDM6A, KMT2C, MYBL1, NOTCH2, NOTCH3
FliC's Hypervariable D3 Domain Is Required for Robust Anti-Flagellin Primary Antibody Responses.
ImmunoHorizons | 2019-09-05 | PMID 31488506
López-Yglesias Américo H, Lu Chun-Chi, Zhao Xiaodan and 4 more
Genes: TLR5
Scaffold-free bioprinted osteogenic and chondrogenic systems to model osteochondral physiology.
Biomedical materials (Bristol, England) | 2019-10-03 | PMID 31491773
Breathwaite Erick K, Weaver Jessica R, Murchison Angela C and 3 more
Genes: MSC
A polygenic resilience score moderates the genetic risk for schizophrenia.
Molecular psychiatry | 2021-03-01 | PMID 31492941
Hess Jonathan L, Tylee Daniel S, Mattheisen Manuel and 21 more
Whole Genome Analyses of Chinese Population and De Novo Assembly of A Northern Han Genome.
Genomics, proteomics & bioinformatics | 2019-06-01 | PMID 31494266
Du Zhenglin, Ma Liang, Qu Hongzhu and 27 more
Genes: MTHFR, FADS1, FADS2, KAT8, TCN2
Facilitation of glutamate, but not GABA, release in Familial Alzheimer's APP mutant Knock-in rats with increased β-cleavage of APP.
Aging cell | 2019-12-01 | PMID 31496118
Tambini Marc D, Yao Wen, D'Adamio Luciano
Genes: APP, BACE1, BAD
Analysis of CDKN1C in fetal growth restriction and pregnancy loss.
F1000Research | 2019-01-01 | PMID 31497289
Suntharalingham Jenifer P, Ishida Miho, Buonocore Federica and 6 more
Sex differences in the genetic predictors of Alzheimer's pathology.
Brain : a journal of neurology | 2019-09-01 | PMID 31497858
Dumitrescu Logan, Barnes Lisa L, Thambisetty Madhav and 35 more
Genes: APOE
The wing of the ToxR winged helix-turn-helix domain is required for DNA binding and activation of toxT and ompU.
PloS one | 2019-01-01 | PMID 31498842
Morgan Sarah J, French Emily L, Plecha Sarah C and 1 more
Loss of PTPN22 abrogates the beneficial effect of cohousing-mediated fecal microbiota transfer in murine colitis.
Mucosal immunology | 2019-11-01 | PMID 31501515
Spalinger Marianne R, Schwarzfischer Marlene, Hering Larissa and 15 more
Genes: PTPN22
Warmblood fragile foal syndrome type 1 mutation (PLOD1 c.2032G>A) is not associated with catastrophic breakdown and has a low allele frequency in the Thoroughbred breed.
Equine veterinary journal | 2020-05-01 | PMID 31502696
Bellone R R, Ocampo N R, Hughes S S and 4 more
Genes: PLOD1
A latent unknown clustering integrating multi-omics data (LUCID) with phenotypic traits.
Bioinformatics (Oxford, England) | 2020-02-01 | PMID 31504184
Peng Cheng, Wang Jun, Asante Isaac and 6 more
SNV identification from single-cell RNA sequencing data.
Human molecular genetics | 2019-11-01 | PMID 31504520
Schnepp Patricia M, Chen Mengjie, Keller Evan T and 1 more
A trans-ancestral meta-analysis of genome-wide association studies reveals loci associated with childhood obesity.
Human molecular genetics | 2019-10-01 | PMID 31504550
Bradfield Jonathan P, Vogelezang Suzanne, Felix Janine F and 96 more
Genes: FAIM2, GNPDA2, MC4R, METTL15, SEC16B
Glycogen storage diseases: Twenty-seven new variants in a cohort of 125 patients.
Molecular genetics & genomic medicine | 2019-11-01 | PMID 31508908
Sperb-Ludwig Fernanda, Pinheiro Franciele Cabral, Bettio Soares Malu and 7 more
Genes: SLC37A4
In utero exposure to maternal diabetes impairs nephron progenitor differentiation.
American journal of physiology. Renal physiology | 2019-11-01 | PMID 31509011
Cerqueira Débora M, Hemker Shelby L, Bodnar Andrew J and 8 more
Ataxia-telangiectasia mutated is required for the development of protective immune memory after influenza A virus infection.
American journal of physiology. Lung cellular and molecular physiology | 2019-11-01 | PMID 31509427
Warren Rachel, Domm William, Yee Min and 5 more
Genes: ATM
A functional role for the cancer disparity-linked genes, CRYβB2 and CRYβB2P1, in the promotion of breast cancer.
Breast cancer research : BCR | 2019-09-11 | PMID 31511085
Barrow Maya A, Martin Megan E, Coffey Alisha and 6 more
Genes: IL6
In vivo epigenetic editing of Sema6a promoter reverses transcallosal dysconnectivity caused by C11orf46/Arl14ep risk gene.
Nature communications | 2019-09-11 | PMID 31511512
Peter Cyril J, Saito Atsushi, Hasegawa Yuto and 16 more
Genes: SEMA6A, SETDB1
Antiviral immunity is impaired in COPD patients with frequent exacerbations.
American journal of physiology. Lung cellular and molecular physiology | 2019-12-01 | PMID 31513433
Singanayagam Aran, Loo Su-Ling, Calderazzo Maria and 14 more
Systematic Review: Clinical Metabolomics to Forecast Outcomes in Liver Transplantation Surgery.
Omics : a journal of integrative biology | 2019-10-01 | PMID 31513460
Attard Joseph A, Dunn Warwick B, Mergental Hynek and 3 more
Differentiation of Mesenchymal Stem Cells to Neuroglia: in the Context of Cell Signalling.
Stem cell reviews and reports | 2019-12-01 | PMID 31515658
George Sajan, Hamblin Michael R, Abrahamse Heidi
[Mutation analysis of 77 patients with normal-karyotype myelodysplastic syndrome].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2019-09-10 | PMID 31515775
Qin Wei, Chen Meiyu, Cai Xiaohui and 9 more
Genes: FLT3, ASXL1, DNMT3A, NPM1, RUNX1, U2AF1, BCOR, CALR
Transcription Factor-Directed Re-wiring of Chromatin Architecture for Somatic Cell Nuclear Reprogramming toward trans-Differentiation.
Molecular cell | 2019-11-07 | PMID 31519520
Dall'Agnese Alessandra, Caputo Luca, Nicoletti Chiara and 11 more
Genes: TF, CTCF
Evaluation of the liquid biopsy for the detection of BRAFV600E mutation in metastatic melanoma patients.
Cancer biomarkers : section A of Disease markers | 2019-01-01 | PMID 31524142
Salvianti Francesca, Massi Daniela, De Giorgi Vincenzo and 3 more
Nanoarray Digital Polymerase Chain Reaction with High-Resolution Melt for Enabling Broad Bacteria Identification and Pheno-Molecular Antimicrobial Susceptibility Test.
Analytical chemistry | 2019-10-15 | PMID 31525952
Athamanolap Pornpat, Hsieh Kuangwen, O'Keefe Christine M and 3 more
A regression framework to uncover pleiotropy in large-scale electronic health record data.
Journal of the American Medical Informatics Association : JAMIA | 2019-10-01 | PMID 31529123
Li Ruowang, Duan Rui, Kember Rachel L and 4 more
Mitochondria, sex and variation in routine metabolic rate.
Molecular ecology | 2019-10-01 | PMID 31529542
Healy Timothy M, Brennan Reid S, Whitehead Andrew and 1 more
NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.
Translational psychiatry | 2019-09-17 | PMID 31530798
Alliey-Rodriguez Ney, Grey Tamar A, Shafee Rebecca and 38 more
Genes: NRXN1
VX-770-mediated potentiation of numerous human CFTR disease mutants is influenced by phosphorylation level.
Scientific reports | 2019-09-17 | PMID 31530897
Cui Guiying, Stauffer Brandon B, Imhoff Barry R and 4 more
Genes: CFTR
Prediction of nutrient digestibility in grower-finisher pigs based on faecal microbiota composition.
Journal of animal breeding and genetics = Zeitschrift fur Tierzuchtung und Zuchtungsbiologie | 2020-01-01 | PMID 31531910
Verschuren Lisanne M G, Schokker Dirkjan, Bergsma Rob and 3 more
MNS1 variant associated with situs inversus and male infertility.
European journal of human genetics : EJHG | 2020-01-01 | PMID 31534215
Leslie Joseph S, Rawlins Lettie E, Chioza Barry A and 10 more
Genes: MNS1, SI
Evaluation of TypeSeq, a Novel High-Throughput, Low-Cost, Next-Generation Sequencing-Based Assay for Detection of 51 Human Papillomavirus Genotypes.
The Journal of infectious diseases | 2019-10-08 | PMID 31536132
Wagner Sarah, Roberson David, Boland Joseph and 17 more
Interrogation of CYP2D6 Structural Variant Alleles Improves the Correlation Between CYP2D6 Genotype and CYP2D6-Mediated Metabolic Activity.
Clinical and translational science | 2020-01-01 | PMID 31536170
Dalton Rachel, Lee Seung-Been, Claw Katrina G and 15 more
Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen.
Journal of the American Society of Nephrology : JASN | 2019-10-01 | PMID 31537649
Salem Rany M, Todd Jennifer N, Sandholm Niina and 85 more
Genes: COL4A3, BMP7, COLEC11, DDR1
Depression genetic risk score is associated with anhedonia-related markers across units of analysis.
Translational psychiatry | 2019-09-19 | PMID 31537779
Guffanti Guia, Kumar Poornima, Admon Roee and 6 more
Marked variation in heritability estimates of left ventricular mass depending on modality of measurement.
Scientific reports | 2019-09-19 | PMID 31537879
Nethononda Richard M, McGurk Kathryn A, Whitworth Polly and 8 more
Association of Birth Weight With Type 2 Diabetes and Glycemic Traits: A Mendelian Randomization Study.
JAMA network open | 2019-09-04 | PMID 31539074
Huang Tao, Wang Tiange, Zheng Yan and 131 more
Functional Domains of the Herpes Simplex Virus Type 1 Tegument Protein pUL37: The Amino Terminus is Dispensable for Virus Replication in Tissue Culture.
Viruses | 2019-09-14 | PMID 31540043
Grzesik Peter, Pryce Erin N, Bhalala Akshay and 6 more
Genes: TRAF6
Regulatory Macrophages Inhibit Alternative Macrophage Activation and Attenuate Pathology Associated with Fibrosis.
Journal of immunology (Baltimore, Md. : 1950) | 2019-10-15 | PMID 31541024
Chandrasekaran Prabha, Izadjoo Salman, Stimely Jessica and 4 more
Genome-Wide Association Study of Apparent Treatment-Resistant Hypertension in the CHARGE Consortium: The CHARGE Pharmacogenetics Working Group.
American journal of hypertension | 2019-11-15 | PMID 31545351
Irvin Marguerite R, Sitlani Colleen M, Floyd James S and 41 more
Genes: CASZ1, MVP
Detection and molecular characterization of urinary tract HIV-1 populations.
Annals of clinical microbiology and antimicrobials | 2019-09-24 | PMID 31551072
Mzingwane M L, Hunt G, Lassauniere R and 8 more
A Polygenic Risk Score for Breast Cancer in US Latinas and Latin American Women.
Journal of the National Cancer Institute | 2020-06-01 | PMID 31553449
Shieh Yiwey, Fejerman Laura, Lott Paul C and 20 more
Posterior reversible encephalopathy syndrome in pediatric patients: pathophysiology, diagnosis, and management.
Leukemia & lymphoma | 2019-10-01 | PMID 31556774
Ghali Michael G Z, Davanzo Justin, Leo Madeline and 1 more
APOL1 Kidney Risk Variants Induce Cell Death via Mitochondrial Translocation and Opening of the Mitochondrial Permeability Transition Pore.
Journal of the American Society of Nephrology : JASN | 2019-12-01 | PMID 31558683
Shah Shrijal S, Lannon Herbert, Dias Leny and 4 more
Genes: APOL1
A call to adopt a "fit for purpose" approach to antibody validation for flow cytometry analyses of stem cell models and beyond.
American journal of physiology. Heart and circulatory physiology | 2019-11-01 | PMID 31559827
Waas Matthew, Gundry Rebekah L
Developmental Outcomes of Aicardi Goutières Syndrome.
Journal of child neurology | 2020-01-01 | PMID 31559893
Adang Laura, Gavazzi Francesco, De Simone Micaela and 11 more
Genes: IFIH1, SAMHD1, TREX1, ADAR, RNASEH2A, RNASEH2B, RNASEH2C
Next-generation sequencing for the diagnosis of MYH9-RD: Predicting pathogenic variants.
Human mutation | 2020-01-01 | PMID 31562665
Bury Loredana, Megy Karyn, Stephens Jonathan C and 34 more
Genes: MYH9
Resolving a clinical tuberculosis outbreak using palaeogenomic genome reconstruction methodologies.
Tuberculosis (Edinburgh, Scotland) | 2019-12-01 | PMID 31563810
Jones Rhys, Velasco Marcela Sandoval, Harris Llinos G and 10 more
AMPK phosphorylation of the β1Pix exchange factor regulates the assembly and function of an ENaC inhibitory complex in kidney epithelial cells.
American journal of physiology. Renal physiology | 2019-12-01 | PMID 31566435
Ho Pei-Yin, Li Hui, Cheng Lei and 3 more
The dual role of ribonucleases in tumor-host relationship.
Experimental oncology | 2019-09-01 | PMID 31569937
Shlyakhovenko V O, Samoylenko О А
Constitutive XBP-1s-mediated activation of the endoplasmic reticulum unfolded protein response protects against pathological tau.
Nature communications | 2019-09-30 | PMID 31570707
Waldherr Sarah M, Strovas Timothy J, Vadset Taylor A and 2 more
Genes: ATF6
CLEC3B p.S106G Mutant in a Caucasian Population of Successful Neurological Aging.
The journals of gerontology. Series A, Biological sciences and medical sciences | 2020-09-16 | PMID 31570938
Kolicheski Ana, Walton Ronald L, Soto-Beasley Alexandra I and 7 more
Genes: CLEC3B, APOE, FOXO3
The prospect of discovering new biomarkers for ovarian cancer based on current knowledge of susceptibility loci and genetic variation (Review).
International journal of molecular medicine | 2019-11-01 | PMID 31573049
Christophersen Mikael Kronborg, Høgdall Claus, Høgdall Estrid
Genes: BRCA1, BRIP1, MSH6, RAD51C, TP53
Haptoglobin-2 variant increases susceptibility to acute respiratory distress syndrome during sepsis.
JCI insight | 2019-11-01 | PMID 31573976
Kerchberger V Eric, Bastarache Julie A, Shaver Ciara M and 12 more
Genes: CFH, HP
Abnormal fertility, acrosome formation, IFT20 expression and localization in conditional Gmap210 knockout mice.
American journal of physiology. Cell physiology | 2020-01-01 | PMID 31577511
Wang Zhenyu, Shi Yuqin, Ma Suheng and 12 more
Genes: IFT20, TRIP11
GATA2 controls lymphatic endothelial cell junctional integrity and lymphovenous valve morphogenesis through miR-126.
Development (Cambridge, England) | 2019-11-05 | PMID 31582413
Mahamud Md Riaj, Geng Xin, Ho Yen-Chun and 17 more
Genes: GATA2
Cumulative inactivation of Nell-1 in Wnt1 expressing cell lineages results in craniofacial skeletal hypoplasia and postnatal hydrocephalus.
Cell death and differentiation | 2020-04-01 | PMID 31582804
Chen Xiaoyan, Wang Huiming, Yu Mengliu and 14 more
Genes: CS
The International Genome Sample Resource (IGSR) collection of open human genomic variation resources.
Nucleic acids research | 2020-01-08 | PMID 31584097
Fairley Susan, Lowy-Gallego Ernesto, Perry Emily and 1 more
Considerations When Using Breast Cancer Risk Models for Women with Negative BRCA1/BRCA2 Mutation Results.
Journal of the National Cancer Institute | 2020-04-01 | PMID 31584660
MacInnis Robert J, Liao Yuyan, Knight Julia A and 22 more
Genes: BRCA1, BRCA2
Automated Platform for Long-Term Culture and High-Content Phenotyping of Single C. elegans Worms.
Scientific reports | 2019-10-04 | PMID 31586133
Atakan H B, Xiang R, Cornaglia M and 4 more
Developmental Trajectories of Infants With Multiplex Family Risk for Autism: A Baby Siblings Research Consortium Study.
JAMA neurology | 2020-01-01 | PMID 31589284
McDonald Nicole M, Senturk Damla, Scheffler Aaron and 17 more
Soft windowing application to improve analysis of high-throughput phenotyping data.
Bioinformatics (Oxford, England) | 2020-03-01 | PMID 31591642
Haselimashhadi Hamed, Mason Jeremy C, Munoz-Fuentes Violeta and 61 more
Improved characterisation of MRSA transmission using within-host bacterial sequence diversity.
eLife | 2019-10-08 | PMID 31591959
Hall Matthew D, Holden Matthew Tg, Srisomang Pramot and 8 more
Cytomegalovirus Genetic Diversity Following Primary Infection.
The Journal of infectious diseases | 2020-02-18 | PMID 31593588
Ross Shannon A, Pati Pravasini, Jensen Travis L and 6 more
International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci.
Nature communications | 2019-10-08 | PMID 31594949
Nievergelt Caroline M, Maihofer Adam X, Klengel Torsten and 176 more
Chromosomal microarray and whole-exome sequence analysis in Taiwanese patients with autism spectrum disorder.
Molecular genetics & genomic medicine | 2019-12-01 | PMID 31595719
Chang Ya-Sian, Lin Chien-Yu, Huang Hsi-Yuan and 2 more
Genes: NHS, SMPD1, BCHE, DUOX2, EYS, FLG, FUT2, JMJD1C
Multi-omics analysis of tumor mutation burden combined with immune infiltrates in bladder urothelial carcinoma.
Journal of cellular physiology | 2020-04-01 | PMID 31596511
Zhang Chuanjie, Shen Luping, Qi Feng and 2 more
Genes: CD4
Pparg promotes differentiation and regulates mitochondrial gene expression in bladder epithelial cells.
Nature communications | 2019-10-09 | PMID 31597917
Liu Chang, Tate Tiffany, Batourina Ekatherina and 13 more
Ensembl Genomes 2020-enabling non-vertebrate genomic research.
Nucleic acids research | 2020-01-08 | PMID 31598706
Howe Kevin L, Contreras-Moreira Bruno, De Silva Nishadi and 52 more
Clinical and Genetic Contributors to New-Onset Atrial Fibrillation in Critically Ill Adults.
Critical care medicine | 2020-01-01 | PMID 31599812
Kerchberger V Eric, Huang Yi, Koyama Tatsuki and 5 more
Genes: PITX2
Inherited variants at 3q13.33 and 3p24.1 are associated with risk of diffuse large B-cell lymphoma and implicate immune pathways.
Human molecular genetics | 2020-01-01 | PMID 31600786
Kleinstern Geffen, Yan Huihuang, Hildebrandt Michelle A T and 35 more
Genes: MAF, AZI2, CD86, EOMES, ILDR1
Heart disease in a mutant mouse model of spontaneous eosinophilic myocarditis maps to three loci.
BMC genomics | 2019-10-11 | PMID 31601172
Zimmermann Nives, Gibbons William J, Homan Shelli M and 1 more