Genetic mechanisms of Coxiella burnetii lipopolysaccharide phase variation.
PLoS pathogens | 2018-03-01 | PMID 29481553
Beare Paul A, Jeffrey Brendan M, Long Carrie M and 2 more
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 7679 of 10600
Mathematical modelling of the antibiotic-induced morphological transition of Pseudomonas aeruginosa.
PLoS computational biology | 2018-02-01 | PMID 29481562
Spalding Chloe, Keen Emma, Smith David J and 2 more
Analysis of age-related changes in psychosine metabolism in the human brain.
PloS one | 2018-01-01 | PMID 29481565
Marshall Michael S, Jakubauskas Benas, Bogue Wil and 9 more
Genes: GALC
17-AAG inhibits vemurafenib-associated MAP kinase activation and is synergistic with cellular immunotherapy in a murine melanoma model.
PloS one | 2018-01-01 | PMID 29481571
Joshi Sandeep S, Jiang Shunlin, Unni Emmanual and 4 more
Genes: BRAF, NRAS, DCT, TYR, TYRP1
Methods for fine-mapping with chromatin and expression data.
PLoS genetics | 2018-02-01 | PMID 29481575
Roytman Megan, Kichaev Gleb, Gusev Alexander and 1 more
Subset of Cortical Layer 6b Neurons Selectively Innervates Higher Order Thalamic Nuclei in Mice.
Cerebral cortex (New York, N.Y. : 1991) | 2018-05-01 | PMID 29481606
Hoerder-Suabedissen Anna, Hayashi Shuichi, Upton Louise and 8 more
The Role of Mitochondrial DNA Variation in Age-Related Decline in Gait Speed Among Older Men Living With Human Immunodeficiency Virus.
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America | 2018-08-16 | PMID 29481608
Sun Jing, Brown Todd T, Samuels David C and 9 more
Evaluation of tools for highly variable gene discovery from single-cell RNA-seq data.
Briefings in bioinformatics | 2019-07-19 | PMID 29481632
Yip Shun H, Sham Pak Chung, Wang Junwen
When Darwin's Special Difficulty Promotes Diversification in Insects.
Systematic biology | 2018-09-01 | PMID 29481653
Legendre Frédéric, Condamine Fabien L
A Common DIO2 Polymorphism and Alzheimer Disease Dementia in African and European Americans.
The Journal of clinical endocrinology and metabolism | 2018-05-01 | PMID 29481662
McAninch Elizabeth A, Rajan Kumar B, Evans Denis A and 6 more
Genes: DIO2
Identification of seven novel loci associated with amino acid levels using single-variant and gene-based tests in 8545 Finnish men from the METSIM study.
Human molecular genetics | 2018-05-01 | PMID 29481666
Teslovich Tanya M, Kim Daniel Seung, Yin Xianyong and 28 more
Genes: MAF, BCAT2, GLDC, HAL, LIPC, PYCR1, TRIB1, WWOX
Pathogenic CTC1 mutations cause global genome instabilities under replication stress.
Nucleic acids research | 2018-05-04 | PMID 29481669
Wang Yuan, Chai Weihang
Genes: CTC1, RAD51, STN1, TEN1
Mechanistic basis of an epistatic interaction reducing age at onset in hereditary spastic paraplegia.
Brain : a journal of neurology | 2018-05-01 | PMID 29481671
Newton Timothy, Allison Rachel, Edgar James R and 17 more
Genes: SPAST
Human RAD51 rapidly forms intrinsically dynamic nucleoprotein filaments modulated by nucleotide binding state.
Nucleic acids research | 2018-05-04 | PMID 29481689
Špírek Mário, Mlcoušková Jarmila, Belán Ondrej and 6 more
Genes: RAD51
Automated Closed-System Expansion of Pluripotent Stem Cell Aggregates in a Rocking-Motion Bioreactor.
SLAS technology | 2018-08-01 | PMID 29481762
Davis Brian M, Loghin Evelina R, Conway Kenneth R and 1 more
Ferrochelatase π-helix: Implications from examining the role of the conserved π-helix glutamates in porphyrin metalation and product release.
Archives of biochemistry and biophysics | 2018-04-15 | PMID 29481781
Gillam Mallory E, Hunter Gregory A, Ferreira Gloria C
First description of a novel mitochondrial mutation in the MT-TI gene associated with multiple mitochondrial DNA deletion and depletion in family with severe dilated mitochondrial cardiomyopathy.
Biochemical and biophysical research communications | 2018-03-18 | PMID 29481798
Alila-Fersi Olfa, Tabebi Mouna, Maalej Marwa and 4 more
Cytochrome C oxydase deficiency: SURF1 gene investigation in patients with Leigh syndrome.
Biochemical and biophysical research communications | 2018-03-18 | PMID 29481804
Maalej Marwa, Kammoun Thouraya, Alila-Fersi Olfa and 7 more
Genes: SURF1
Panel Sequencing Shows Recurrent Genetic FAS Alterations in Primary Cutaneous Marginal Zone Lymphoma.
The Journal of investigative dermatology | 2018-07-01 | PMID 29481902
Maurus Katja, Appenzeller Silke, Roth Sabine and 8 more
Genes: FAS, NCOR2, SLAMF1, SPEN
Novel mutation in a family with WNT1-related osteoporosis.
European journal of medical genetics | 2018-07-01 | PMID 29481978
Panigrahi Inusha, Didel Siyaram, Kirpal Harita and 4 more
Genes: WNT1, BMP1, CRTAP, SERPINH1
IL10 promoter haplotypes may contribute to altered cytokine expression and systemic inflammation in celiac disease.
Clinical immunology (Orlando, Fla.) | 2018-05-01 | PMID 29481982
Hofmann S R, Laass M W, Fehrs A and 5 more
Lower frequency of the HLA-G UTR-4 haplotype in women with unexplained recurrent miscarriage.
Journal of reproductive immunology | 2018-04-01 | PMID 29481987
Meuleman T, Drabbels J, van Lith J M M and 6 more
Biology and function of adipose tissue macrophages, dendritic cells and B cells.
Atherosclerosis | 2018-04-01 | PMID 29482037
Ivanov Stoyan, Merlin Johanna, Lee Man Kit Sam and 2 more
Genes: ATM
A genetic association study of carotid intima-media thickness (CIMT) and plaque in Mexican Americans and European Americans with rheumatoid arthritis.
Atherosclerosis | 2018-04-01 | PMID 29482039
Arya Rector, Escalante Agustin, Farook Vidya S and 12 more
Genes: PPCDC
A change in structural integrity of c-Kit mutant D816V causes constitutive signaling.
Mutation research | 2018-03-01 | PMID 29482074
Raghav Pawan Kumar, Singh Ajay Kumar, Gangenahalli Gurudutta
Kit-dependent discrepancy in D16S539 and general considerations for database matches.
Forensic science international. Genetics | 2018-05-01 | PMID 29482104
Zajac Barbara Karolina, Zehner Richard, Scheiper Stefanie and 1 more
New acrylamide-substituted quinazoline derivatives with enhanced potency for the treatment of EGFR T790M-mutant non-small-cell lung cancers.
Bioorganic chemistry | 2018-04-01 | PMID 29482151
Liu Zhuo, Wang Luhong, Feng Min and 7 more
Genes: EGFR
Efficacy of Exome-Targeted Capture Sequencing to Detect Mutations in Known Cerebellar Ataxia Genes.
JAMA neurology | 2018-05-01 | PMID 29482223
Coutelier Marie, Hammer Monia B, Stevanin Giovanni and 32 more
Genes: ERCC5, KCND3, SACS, SETX, SPG7
Tumor Protein p53 (TP53) Gene and Left Main Coronary Artery Disease.
Angiology | 2018-09-01 | PMID 29482350
Kolovou Vana, Tsipis Angelos, Mihas Constantinos and 8 more
Genes: CAD
The effect of troxerutin on anxiety- and depressive-like behaviours in the offspring of high-fat diet fed dams.
Archives of physiology and biochemistry | 2019-05-01 | PMID 29482367
Bayandor Parvin, Farajdokht Fereshteh, Mohaddes Gisou and 5 more
Potential Role of ADRA2A Genetic Variants in the Etiology of ADHD Comorbid With Tic Disorders.
Journal of attention disorders | 2021-01-01 | PMID 29482474
Xu Defeng, Liu Lu, Li Haimei and 4 more
Difficult diagnosis and genetic analysis of fibrodysplasia ossificans progressiva: a case report.
BMC medical genetics | 2018-02-27 | PMID 29482508
Tian Shengjie, Zhu Jianhua, Lu Yaogang
Genes: ACVR1
Exploring the arthritogenicity of Streptococcus dysgalactiae subspecies equisimilis.
BMC microbiology | 2018-02-27 | PMID 29482512
Oppegaard Oddvar, Mylvaganam Haima, Skrede Steinar and 1 more
Expansion of phenotypic spectrum of MYO15A pathogenic variants to include postlingual onset of progressive partial deafness.
BMC medical genetics | 2018-02-27 | PMID 29482514
Chang Mun Young, Lee Chung, Han Jin Hee and 6 more
Genes: TES
Identification of novel KMT2D mutations in two Chinese children with Kabuki syndrome: a case report and systematic literature review.
BMC medical genetics | 2018-02-27 | PMID 29482518
Xin Chengqi, Wang Chun, Wang Yachen and 4 more
The association of Val109Asp polymorphic marker of intelectin 1 gene with abdominal obesity in Kyrgyz population.
BMC endocrine disorders | 2018-02-27 | PMID 29482534
Isakova Jainagul, Talaibekova Elnura, Vinnikov Denis and 3 more
Genes: ITLN1
Genetic risk for Alzheimer's disease is concentrated in specific macrophage and microglial transcriptional networks.
Genome medicine | 2018-02-26 | PMID 29482603
Tansey Katherine E, Cameron Darren, Hill Matthew J
Genes: SPI1
Population-based analysis of ocular Chlamydia trachomatis in trachoma-endemic West African communities identifies genomic markers of disease severity.
Genome medicine | 2018-02-26 | PMID 29482619
Last A R, Pickering H, Roberts C H and 14 more
One-step genetic correction of hemoglobin E/beta-thalassemia patient-derived iPSCs by the CRISPR/Cas9 system.
Stem cell research & therapy | 2018-02-26 | PMID 29482624
Wattanapanitch Methichit, Damkham Nattaya, Potirat Ponthip and 6 more
Genes: HBB
LRRK2 mediated Rab8a phosphorylation promotes lipid storage.
Lipids in health and disease | 2018-02-27 | PMID 29482628
Yu Miao, Arshad Muhammad, Wang Wenmin and 3 more
Independent functions of DNMT1 and USP7 at replication foci.
Epigenetics & chromatin | 2018-02-27 | PMID 29482658
Yarychkivska Olya, Tavana Omid, Gu Wei and 1 more
Genes: DNMT1, USP7, PCNA
TRAPPED - an insight into two sisters' struggle to access treatment for a rare genetic disease.
Orphanet journal of rare diseases | 2018-02-27 | PMID 29482660
Al-Attar Mariam
Genes: NHS
Does thinner right entorhinal cortex underlie genetic liability to cannabis use?
Psychological medicine | 2018-12-01 | PMID 29482671
Paul Subhadip, Bhattacharyya Sagnik
Pseudohypoaldosteronism Type II: A Young Girl Presented with Hypertension, Hyperkalemia and Metabolic Acidosis.
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP | 2018-03-01 | PMID 29482694
Sethar Gul Hassan, Almoghawi Aisha, Khan Nargis and 2 more
Genes: KLHL3, WNK1, WNK4
The SWI/SNF complex subunit genes: Their functions, variations, and links to risk and survival outcomes in human cancers.
Critical reviews in oncology/hematology | 2018-03-01 | PMID 29482773
Savas Sevtap, Skardasi Georgia
Resistance to EGFR inhibitors in non-small cell lung cancer: Clinical management and future perspectives.
Critical reviews in oncology/hematology | 2018-03-01 | PMID 29482776
Tomasello Chiara, Baldessari Cinzia, Napolitano Martina and 5 more
Genes: EGFR
The stem cell division theory of cancer.
Critical reviews in oncology/hematology | 2018-03-01 | PMID 29482784
López-Lázaro Miguel
SARS-CoV related Betacoronavirus and diverse Alphacoronavirus members found in western old-world.
Virology | 2018-04-01 | PMID 29482919
Ar Gouilh Meriadeg, Puechmaille Sébastien J, Diancourt Laure and 8 more
Association of Ring Finger Protein 213 Gene P.R4810k Polymorphism with Intracranial Major Artery Stenosis/Occlusion.
Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association | 2018-06-01 | PMID 29482934
Zhang Qian, Yu Lebao, Ge Peicong and 10 more
Pharmacogenetics as Personalized Medicine: Association Investigation of SOD2 rs4880, CYP2C19 rs4244285, and FCGR2A rs1801274 Polymorphisms in a Breast Cancer Population in Iraqi Women.
Clinical breast cancer | 2018-10-01 | PMID 29482947
Jabir Ferdous A, Hoidy Wisam H
Genes: SOD2
Immunohistochemical evaluation of H3K27 trimethylation in malignant peripheral nerve sheath tumors.
Pathology, research and practice | 2018-03-01 | PMID 29482987
Otsuka Hiroshi, Kohashi Kenichi, Yoshimoto Masato and 6 more
Genes: EED, SUZ12
Clinical presentation and treatment paradigms of brain arteriovenous malformations in patients with hereditary hemorrhagic telangiectasia.
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia | 2018-05-01 | PMID 29483005
Gamboa Nicholas T, Joyce Evan J, Eli Ilyas and 6 more
Genes: ACVRL1, ENG
Desmin Phosphorylation Triggers Preamyloid Oligomers Formation and Myocyte Dysfunction in Acquired Heart Failure.
Circulation research | 2018-05-11 | PMID 29483093
Rainer Peter P, Dong Peihong, Sorge Matteo and 13 more
The Clarithromycin Susceptibility Genotype Affects the Treatment Outcome of Patients with Mycobacterium abscessus Lung Disease.
Antimicrobial agents and chemotherapy | 2018-05-01 | PMID 29483126
Guo Qi, Chu Haiqing, Ye Meiping and 5 more
Allele-Specific Mechanisms of Activation of MEK1 Mutants Determine Their Properties.
Cancer discovery | 2018-05-01 | PMID 29483135
Gao Yijun, Chang Matthew T, McKay Daniel and 15 more
C. elegans ADARs antagonize silencing of cellular dsRNAs by the antiviral RNAi pathway.
Genes & development | 2018-02-01 | PMID 29483152
Reich Daniel P, Tyc Katarzyna M, Bass Brenda L
HLA-B*07, HLA-DRB1*07, HLA-DRB1*12, and HLA-C*03:02 Strongly Associate With BMI: Data From 1.3 Million Healthy Chinese Adults.
Diabetes | 2018-05-01 | PMID 29483183
Shen Jie, Guo Tingwei, Wang Tao and 47 more
Childhood BMI and Adult Type 2 Diabetes, Coronary Artery Diseases, Chronic Kidney Disease, and Cardiometabolic Traits: A Mendelian Randomization Analysis.
Diabetes care | 2018-05-01 | PMID 29483184
Geng Tingting, Smith Caren E, Li Changwei and 1 more
Genes: CAD
Impact of Chemical-Induced Mutational Load Increase on Immune Checkpoint Therapy in Poorly Responsive Murine Tumors.
Molecular cancer therapeutics | 2018-04-01 | PMID 29483207
Kuczynski Elizabeth A, Krueger Janna, Chow Annabelle and 6 more
Analysis of Tissue and Circulating Tumor DNA by Next-Generation Sequencing of Hepatocellular Carcinoma: Implications for Targeted Therapeutics.
Molecular cancer therapeutics | 2018-05-01 | PMID 29483209
Ikeda Sadakatsu, Lim Jordan S, Kurzrock Razelle
Antitumor Activity of Osimertinib, an Irreversible Mutant-Selective EGFR Tyrosine Kinase Inhibitor, in NSCLC Harboring EGFR Exon 20 Insertions.
Molecular cancer therapeutics | 2018-05-01 | PMID 29483211
Floc'h Nicolas, Martin Matthew J, Riess Jonathan W and 15 more
Genes: EGFR
The Unfolded Protein Response: A Novel Therapeutic Target for Poor Prognostic BRAF Mutant Colorectal Cancer.
Molecular cancer therapeutics | 2018-06-01 | PMID 29483217
Forsythe Nicholas, Refaat Alaa, Javadi Arman and 12 more
Genes: BRAF, EGFR, HDAC6
Targeting PRPK Function Blocks Colon Cancer Metastasis.
Molecular cancer therapeutics | 2018-05-01 | PMID 29483219
Zykova Tatyana, Zhu Feng, Wang Lei and 14 more
Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ≈43% of 35 Families With Midaortic Syndrome.
Hypertension (Dallas, Tex. : 1979) | 2018-04-01 | PMID 29483232
Warejko Jillian K, Schueler Markus, Vivante Asaf and 25 more
Genes: ELN, GATA6, JAG1
Penetrance estimates for BRCA1, BRCA2 (also applied to Lynch syndrome) based on presymptomatic testing: a new unbiased method to assess risk?
Journal of medical genetics | 2018-07-01 | PMID 29483236
Evans D Gareth, Woodward Emma, Harkness Elaine F and 5 more
Genes: BRCA1, BRCA2, MLH1, MSH2
Rapid regulatory evolution of a nonrecombining autosome linked to divergent behavioral phenotypes.
Proceedings of the National Academy of Sciences of the United States of America | 2018-03-13 | PMID 29483264
Sun Dan, Huh Iksoo, Zinzow-Kramer Wendy M and 2 more
The Histone Variant MacroH2A Blocks Cellular Reprogramming by Inhibiting Mesenchymal-to-Epithelial Transition.
Molecular and cellular biology | 2018-05-15 | PMID 29483300
Pliatska Maria, Kapasa Maria, Kokkalis Antonis and 2 more
Genes: MET
Genetics of biologically based psychological differences.
Philosophical transactions of the Royal Society of London. Series B, Biological sciences | 2018-04-19 | PMID 29483347
Sallis Hannah, Davey Smith George, Munafò Marcus R
What is the natural measurement unit of temperament: single traits or profiles?
Philosophical transactions of the Royal Society of London. Series B, Biological sciences | 2018-04-19 | PMID 29483348
Cloninger C Robert, Zwir Igor
Genome-wide association study of loss of heterozygosity and metastasis-free survival in breast cancer patients.
Experimental oncology | 2017-07-01 | PMID 29483489
Deryusheva I V, Tsyganov M, Garbukov E Y and 5 more
Genes: CYSLTR1, PGK1
Expression of cancer-associated genes in prostate tumors.
Experimental oncology | 2017-07-01 | PMID 29483498
Rosenberg E E, Gerashchenko G V, Hryshchenko N V and 7 more
Genes: EFNA5, FOS, PLAU, TGFB1, EPDR1, TAGLN
Allelic decomposition and exact genotyping of highly polymorphic and structurally variant genes.
Nature communications | 2018-02-26 | PMID 29483503
Numanagić Ibrahim, Malikić Salem, Ford Michael and 8 more
Cardiolipin exposure on the outer mitochondrial membrane modulates α-synuclein.
Nature communications | 2018-02-26 | PMID 29483518
Ryan Tammy, Bamm Vladimir V, Stykel Morgan G and 8 more
Genes: SNCA
Characterization of the quinol-dependent nitric oxide reductase from the pathogen Neisseria meningitidis, an electrogenic enzyme.
Scientific reports | 2018-02-26 | PMID 29483528
Gonska Nathalie, Young David, Yuki Riki and 8 more
Comprehensive integrative analyses identify GLT8D1 and CSNK2B as schizophrenia risk genes.
Nature communications | 2018-02-26 | PMID 29483533
Yang Cui-Ping, Li Xiaoyan, Wu Yong and 14 more
Genes: ALMS1
Somatic Mitochondrial DNA Mutations in Diffuse Large B-Cell Lymphoma.
Scientific reports | 2018-02-26 | PMID 29483551
Zeng Andy G X, Leung Andy C Y, Brooks-Wilson Angela R
Self-interaction of NPM1 modulates multiple mechanisms of liquid-liquid phase separation.
Nature communications | 2018-02-26 | PMID 29483575
Mitrea Diana M, Cika Jaclyn A, Stanley Christopher B and 7 more
Genes: NPM1
How ligand binds to the type 1 insulin-like growth factor receptor.
Nature communications | 2018-02-26 | PMID 29483580
Xu Yibin, Kong Geoffrey K-W, Menting John G and 7 more
CRISPR/cas9 mediated knockout of an intergenic variant rs6927172 identified IL-20RA as a new risk gene for multiple autoimmune diseases.
Genes and immunity | 2019-02-01 | PMID 29483615
Wu Jianfeng, Yang Sirui, Yu Di and 9 more
Genes: TNFAIP3
Dysregulation of RNF213 promotes cerebral hypoperfusion.
Scientific reports | 2018-02-26 | PMID 29483617
Morimoto Takaaki, Enmi Jun-Ichiro, Hattori Yorito and 12 more
The efficacy of Ranolazine on E1784K is altered by temperature and calcium.
Scientific reports | 2018-02-26 | PMID 29483621
Abdelsayed Mena, Ruprai Manpreet, Ruben Peter C
New considerations for hiPSC-based models of neuropsychiatric disorders.
Molecular psychiatry | 2019-01-01 | PMID 29483625
Hoffman Gabriel E, Schrode Nadine, Flaherty Erin and 1 more
Targeted Mutation of NGN3 Gene Disrupts Pancreatic Endocrine Cell Development in Pigs.
Scientific reports | 2018-02-26 | PMID 29483633
Sheets Timothy P, Park Ki-Eun, Park Chi-Hun and 4 more
Genes: NEUROD1, PAX4
Resistance to nonribosomal peptide antibiotics mediated by D-stereospecific peptidases.
Nature chemical biology | 2018-04-01 | PMID 29483640
Li Yong-Xin, Zhong Zheng, Hou Peng and 2 more
Directed evolution of a synthetic phylogeny of programmable Trp repressors.
Nature chemical biology | 2018-04-01 | PMID 29483643
Ellefson Jared W, Ledbetter Michael P, Ellington Andrew D
Structural basis for GTP hydrolysis and conformational change of MFN1 in mediating membrane fusion.
Nature structural & molecular biology | 2018-03-01 | PMID 29483649
Yan Liming, Qi Yuanbo, Huang Xiaofang and 6 more
Genes: MFN1
Cryo-EM and X-ray structures of TRPV4 reveal insight into ion permeation and gating mechanisms.
Nature structural & molecular biology | 2018-03-01 | PMID 29483651
Deng Zengqin, Paknejad Navid, Maksaev Grigory and 4 more
Genes: TRPV4
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.
Nature genetics | 2018-03-01 | PMID 29483656
Pardiñas Antonio F, Holmans Peter, Pocklington Andrew J and 66 more
At-risk individuals display altered brain activity following stress.
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology | 2018-08-01 | PMID 29483659
van Leeuwen J M C, Vink M, Fernández G and 4 more
Genes: MCC
Historical changes in grassland area determined the demography of semi-natural grassland butterflies in Japan.
Heredity | 2018-08-01 | PMID 29483662
Nakahama Naoyuki, Uchida Kei, Ushimaru Atushi and 1 more
The association between cancer family history and ovarian cancer risk in BRCA1/2 mutation carriers: can it be explained by the mutation position?
European journal of human genetics : EJHG | 2018-06-01 | PMID 29483665
Teixeira Natalia, van der Hout Annemieke, Oosterwijk Jan C and 11 more
Genes: BRCA1, BRCA2
Uncovering the genetic lesions underlying the most severe form of Hirschsprung disease by whole-genome sequencing.
European journal of human genetics : EJHG | 2018-06-01 | PMID 29483666
Tang Clara Sm, Zhuang Xuehan, Lam Wai-Yee and 9 more
Genes: CCT2, ERBB4, NRG1, VASH1
Whole-exome sequence analysis highlights the role of unmasked recessive mutations in copy number variants with incomplete penetrance.
European journal of human genetics : EJHG | 2018-06-01 | PMID 29483668
Egloff Matthieu, Nguyen Lam-Son, Siquier-Pernet Karine and 8 more
Genes: NCOR1
Genetic determinants of glycated hemoglobin levels in the Greenlandic Inuit population.
European journal of human genetics : EJHG | 2018-06-01 | PMID 29483669
Appel Emil V R, Moltke Ida, Jørgensen Marit E and 6 more
Genes: ANK1, GCK
Novel variants in Nordic patients referred for genetic testing of telomere-related disorders.
European journal of human genetics : EJHG | 2018-06-01 | PMID 29483670
Norberg Anna, Rosén Anna, Raaschou-Jensen Klas and 11 more
Genes: TERT, DKC1, TINF2
New insights from Thailand into the maternal genetic history of Mainland Southeast Asia.
European journal of human genetics : EJHG | 2018-06-01 | PMID 29483671
Kutanan Wibhu, Kampuansai Jatupol, Brunelli Andrea and 10 more
Nature vs. nurture in human sociality: multi-level genomic analyses of social conformity.
Journal of human genetics | 2018-05-01 | PMID 29483675
Chen Biqing, Zhu Zijian, Wang Yingying and 13 more
Genes: NAV3, ARL10, CTNND2, PTPRD
The second point mutation in PREPL: a case report and literature review.
Journal of human genetics | 2018-05-01 | PMID 29483676
Silva Sebastian, Miyake Noriko, Tapia Carolina and 1 more
Genes: PREPL
Could inherited predisposition drive non-obese fatty liver disease? Results from German tertiary referral centers.
Journal of human genetics | 2018-05-01 | PMID 29483677
Krawczyk Marcin, Bantel Heike, Rau Monika and 9 more
Genes: PNPLA3, MBOAT7
Universal genetic testing for inherited susceptibility in children and adults with myelodysplastic syndrome and acute myeloid leukemia: are we there yet?
Leukemia | 2018-07-01 | PMID 29483711
Tawana Kiran, Drazer Michael W, Churpek Jane E
Genes: GATA2, RUNX1