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 7367 of 10600

The CNDP1 (CTG)5 Polymorphism Is Associated with Biopsy-Proven Diabetic Nephropathy, Time on Hemodialysis, and Diabetes Duration.
Journal of diabetes research | 2017-01-01 | PMID 28553654
Albrecht Thomas, Zhang Shiqi, Braun Jana D and 13 more
Genes: CNDP1, CIC
Cancer Is to Embryology as Mutation Is to Genetics: Hypothesis of the Cancer as Embryological Phenomenon.
TheScientificWorldJournal | 2017-01-01 | PMID 28553657
Cofre Jaime, Abdelhay Eliana
Evidence for a Long-Lasting Compulsive Alcohol Seeking Phenotype in Rats.
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology | 2018-03-01 | PMID 28553834
Giuliano Chiara, Peña-Oliver Yolanda, Goodlett Charles R and 5 more
The relationship between levels of plasma-soluble urokinase plasminogen activator receptor (suPAR) and presence of migraine attack and aura.
Journal of receptor and signal transduction research | 2017-10-01 | PMID 28553881
Yılmaz Nigar, Yılmaz Mustafa, Sirin Burcu and 2 more
Genes: CRP
Combined mutation in Vhl, Trp53 and Rb1 causes clear cell renal cell carcinoma in mice.
Nature medicine | 2017-07-01 | PMID 28553932
Harlander Sabine, Schönenberger Désirée, Toussaint Nora C and 6 more
Genes: VHL
Phenotypic screening identifies Axl kinase as a negative regulator of an alveolar epithelial cell phenotype.
Laboratory investigation; a journal of technical methods and pathology | 2017-09-01 | PMID 28553934
Fujino Naoya, Kubo Hiroshi, Maciewicz Rose A
Genes: HOXA5, SNAI2, TBX2, TBX3
Stem cell plasticity enables hair regeneration following Lgr5+ cell loss.
Nature cell biology | 2017-06-01 | PMID 28553937
Hoeck Joerg D, Biehs Brian, Kurtova Antonina V and 7 more
The A946T variant of the RNA sensor IFIH1 mediates an interferon program that limits viral infection but increases the risk for autoimmunity.
Nature immunology | 2017-07-01 | PMID 28553952
Gorman Jacquelyn A, Hundhausen Christian, Errett John S and 17 more
Genes: IFIH1
Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.
Nature genetics | 2017-07-01 | PMID 28553957
Aung Tin, Ozaki Mineo, Lee Mei Chin and 286 more
Genes: LOXL1, AGPAT1, POMP, RBMS3
Polygenic burdens on cell-specific pathways underlie the risk of rheumatoid arthritis.
Nature genetics | 2017-07-01 | PMID 28553958
Ishigaki Kazuyoshi, Kochi Yuta, Suzuki Akari and 21 more
Genes: TNF
Biallelic TRIP13 mutations predispose to Wilms tumor and chromosome missegregation.
Nature genetics | 2017-07-01 | PMID 28553959
Yost Shawn, de Wolf Bas, Hanks Sandra and 18 more
Genes: TRIP13, CEP57
Splicing-related single nucleotide polymorphism of RAB, member of RAS oncogene family like 2B (RABL2B) jeopardises semen quality in Chinese Holstein bulls.
Reproduction, fertility, and development | 2017-11-01 | PMID 28553998
Wang Xiuge, Cui Xiaohui, Zhang Yan and 9 more
Association of TP53 codon 72 and CDH1 genetic polymorphisms with colorectal cancer risk in Bangladeshi population.
Cancer epidemiology | 2017-08-01 | PMID 28554075
Rivu Sanzana Fareen, Apu Mohd Nazmul Hasan, Shabnaz Samia and 8 more
Genes: CDH1
Association between obesity phenotypes and incident hypertension among Chinese adults: a prospective cohort study.
Public health | 2017-08-01 | PMID 28554164
Cao Z K, Huang Y, Yu H J and 6 more
Skin-Dominant Phenotype in a Patient with H Syndrome: Identification of a Novel Mutation in the SLC29A3 Gene.
Cytogenetic and genome research | 2017-01-01 | PMID 28554179
Vural Seçil, Ertop Pelin, Durmaz Ceren D and 5 more
Structure of the human multidrug transporter ABCG2.
Nature | 2017-06-22 | PMID 28554189
Taylor Nicholas M I, Manolaridis Ioannis, Jackson Scott M and 3 more
Genes: ABCG2
Genetic variants and clinical relevance associated with gestational diabetes mellitus in Chinese women: a case-control study.
The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians | 2018-08-01 | PMID 28554271
Yan Jie, Su Rina, Ao Deng and 3 more
Genes: ARHGEF11, PLXND1
Angiogenesis in JAK2 V617F positive myeloproliferative neoplasms and ruxolitinib decrease VEGF, HIF-1 enesis in JAK2 V617F positive cells.
Leukemia & lymphoma | 2018-01-01 | PMID 28554272
Cheng Zhiyong, Fu Jianzhu, Liu Guimin and 3 more
Genes: JAK2, MVD, ABL1, BCR
Calcium Signaling, PKC Gamma, IP3R1 and CAR8 Link Spinocerebellar Ataxias and Purkinje Cell Dendritic Development.
Current neuropharmacology | 2018-01-30 | PMID 28554312
Shimobayashi Etsuko, Kapfhammer Josef P
Genes: PRKCG
Genomic diagnosis for children with intellectual disability and/or developmental delay.
Genome medicine | 2017-05-30 | PMID 28554332
Bowling Kevin M, Thompson Michelle L, Amaral Michelle D and 19 more
OsCOL16, encoding a CONSTANS-like protein, represses flowering by up-regulating Ghd7 expression in rice.
Plant science : an international journal of experimental plant biology | 2017-07-01 | PMID 28554475
Wu Weixun, Zheng Xiao-Ming, Chen Daibo and 13 more
Genes: RFT1
SGD1, a key enzyme in tocopherol biosynthesis, is essential for plant development and cold tolerance in rice.
Plant science : an international journal of experimental plant biology | 2017-07-01 | PMID 28554480
Wang Di, Wang Yunlong, Long Wuhua and 11 more
Candidate gene analysis for Alzheimer's disease in adults with Down syndrome.
Neurobiology of aging | 2017-08-01 | PMID 28554490
Lee Joseph H, Lee Annie J, Dang Lam-Ha and 9 more
Genes: CST3, MARK4, APOE, APP
Expanding the phenotypic spectrum associated with mutations of DYNC1H1.
Neuromuscular disorders : NMD | 2017-07-01 | PMID 28554554
Beecroft Sarah J, McLean Catriona A, Delatycki Martin B and 8 more
Genes: BICD2
Novel truncating variant in DNA2-related congenital onset myopathy and ptosis suggests genotype-phenotype correlation.
Neuromuscular disorders : NMD | 2017-07-01 | PMID 28554558
Phowthongkum P, Sun A
Genes: DNA2
Environmental heterogeneity and the evolution of plant-virus interactions: Viruses in wild pepper populations.
Virus research | 2017-09-15 | PMID 28554561
Fraile Aurora, McLeish Michael J, Pagán Israel and 3 more
Identification and pathotypical analysis of a novel VIk sub-genotype Newcastle disease virus obtained from pigeon in China.
Virus research | 2017-06-15 | PMID 28554562
Xue Cong, Xu Xiaohong, Yin Renfu and 9 more
Evolutionary perspectives on ageing.
Seminars in cell & developmental biology | 2017-10-01 | PMID 28554569
Reichard Martin
Sex-specific lifespan and its evolution in nematodes.
Seminars in cell & developmental biology | 2017-10-01 | PMID 28554570
Ancell Henry, Pires-daSilva Andre
Activity modulation of the oligopeptidase B from Serratia proteamaculans by site-directed mutagenesis of amino acid residues surrounding catalytic triad histidine.
Biochimie | 2017-08-01 | PMID 28554571
Mikhailova Anna G, Rakitina Tatiana V, Timofeev Vladimir I and 7 more
Hepatitis C virus core antigen: A potential alternative to HCV RNA testing among persons with substance use disorders.
Journal of substance abuse treatment | 2017-07-01 | PMID 28554601
Talal Andrew H, Chen Yang, Zeremski Marija and 6 more
The composition of bioactive compounds and antioxidant activity of Saskatoon berry (Amelanchier alnifolia Nutt.) genotypes grown in central Poland.
Food chemistry | 2017-11-15 | PMID 28554632
Lachowicz Sabina, Oszmiański Jan, Pluta Stanisław
Liver and Cardiovascular Damage in Patients With Lean Nonalcoholic Fatty Liver Disease, and Association With Visceral Obesity.
Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association | 2017-10-01 | PMID 28554682
Fracanzani Anna Ludovica, Petta Salvatore, Lombardi Rosa and 10 more
Genes: PNPLA3
New treatments targeting the basic defects in cystic fibrosis.
Presse medicale (Paris, France : 1983) | 2017-06-01 | PMID 28554723
Fajac Isabelle, Wainwright Claire E
Genes: CFTR
Correlation between phenotypic antibiotic susceptibility and the resistome in Pseudomonas aeruginosa.
International journal of antimicrobial agents | 2017-08-01 | PMID 28554735
Jaillard Magali, van Belkum Alex, Cady Kyle C and 12 more
Genomic profiling of esophageal squamous cell carcinoma (ESCC)-Basis for precision medicine.
Pathology, research and practice | 2017-07-01 | PMID 28554745
Yang Jung Wook, Choi Yoon-La
Genes: ERBB2, EGFR, NOTCH1, AKT2, FGFR1, KRAS, MDM2, MTOR
EGFR and KRAS molecular genotyping for pulmonary carcinomas: Feasibility of a simple and rapid technique implementable in any department of pathology.
Pathology, research and practice | 2017-07-01 | PMID 28554746
Thomas De Montpréville Vincent, Ghigna Maria-Rosa, Lacroix Ludovic and 6 more
Genes: EGFR, KRAS
Characterization of common and rare mutations in EGFR and associated clinicopathological features in a large population of Chinese patients with lung cancer.
Pathology, research and practice | 2017-07-01 | PMID 28554755
Wei Bing, Ren Pengfei, Zhang Chengjuan and 7 more
Genes: EGFR
Effect of plasma-activated medium on the decrease of tumorigenic population in lymphoma.
Pathology, research and practice | 2017-07-01 | PMID 28554762
Wada Naoki, Ikeda Jun-Ichiro, Tanaka Hiromasa and 4 more
Genes: PAM, LPL
Characterization of rhodamine 123 low staining cells and their dynamic changes during the injured-repaired progress induced by 5-FU.
Pathology, research and practice | 2017-07-01 | PMID 28554763
Luo Yuqi, Yu Haitao, Ou Wentao and 2 more
Pigmented trichoblastoma developed in a sebaceous nevus: HRAS mutation as a common molecular driver.
Pathology, research and practice | 2017-07-01 | PMID 28554764
Saraggi Deborah, Salmaso Roberto, Valentini Elisa and 5 more
Genes: HRAS, BRAF, KRAS, NRAS
Influence of low frequency PSEN1 variants on familial Alzheimer's disease risk in Brazil.
Neuroscience letters | 2017-07-13 | PMID 28554858
Abdala Bianca Barbosa, Dos Santos Jussara Mendonça, Gonçalves Andressa Pereira and 5 more
Genes: PSEN1, APOE
A novel deletion of SNURF/SNRPN exon 1 in a patient with Prader-Willi-like phenotype.
European journal of medical genetics | 2017-08-01 | PMID 28554868
Cao Yang, AlHumaidi Susan S, Faqeih Eissa A and 3 more
Genes: SNRPN
Pathogenicity of three genetically diverse strains of PRRSV Type 1 in specific pathogen free pigs.
Veterinary microbiology | 2017-09-01 | PMID 28554869
Stadejek Tomasz, Larsen Lars E, Podgórska Katarzyna and 10 more
Genes: APP
Heart failure and endothelial nitric oxide synthase G894T gene polymorphism frequency variations within ancestries.
Nitric oxide : biology and chemistry | 2018-02-28 | PMID 28554876
Oliveira Romulo V M, Albuquerque Felipe N, Duque Gustavo S and 6 more
Portomesenteric venous thrombosis complicated by a haemorrhagic shock: a rare complication of laparoscopic gastrectomy.
BMJ case reports | 2017-05-29 | PMID 28554887
Copelin Eddie, Cholankeril Rosann, Somasundar Ponnandai and 1 more
MSTO1 is a cytoplasmic pro-mitochondrial fusion protein, whose mutation induces myopathy and ataxia in humans.
EMBO molecular medicine | 2017-07-01 | PMID 28554942
Gal Aniko, Balicza Peter, Weaver David and 9 more
Genes: MSTO1
Genetic background and evolution of relapses in aggressive B-cell lymphomas.
Haematologica | 2017-07-01 | PMID 28554945
Juskevicius Darius, Dirnhofer Stephan, Tzankov Alexandar
Enhancement of Biomass and Lipid Productivities of Water Surface-Floating Microalgae by Chemical Mutagenesis.
Marine drugs | 2017-05-27 | PMID 28555001
Nojima Daisuke, Ishizuka Yuki, Muto Masaki and 6 more
The IL-6 Gene Promoter SNP and Plasma IL-6 in Response to Diet Intervention.
Nutrients | 2017-05-27 | PMID 28555011
Rana Brinda K, Flatt Shirley W, Health Dennis D and 4 more
FADS Gene Polymorphisms, Fatty Acid Desaturase Activities, and HDL-C in Type 2 Diabetes.
International journal of environmental research and public health | 2017-05-28 | PMID 28555039
Huang Meng-Chuan, Chang Wen-Tsan, Chang Hsin-Yu and 5 more
Genes: FADS1, FADS2
Association Between Protein Tyrosine Phosphatase Non-Receptor Type 22 (PTPN22) Polymorphisms and Risk of Ankylosing Spondylitis: A Meta-analysis.
Medical science monitor : international medical journal of experimental and clinical research | 2017-05-30 | PMID 28555069
Wang Weiming, Meng Xiantao, Liu Yupeng and 5 more
Genes: PTPN22
Comparative genomic evidence for the involvement of schizophrenia risk genes in antipsychotic effects.
Molecular psychiatry | 2018-03-01 | PMID 28555076
Kim Y, Giusti-Rodriguez P, Crowley J J and 9 more
Genomic determinants of chronic myelomonocytic leukemia.
Leukemia | 2017-12-01 | PMID 28555081
Patel B J, Przychodzen B, Thota S and 18 more
Genes: TET2, ASXL1, SRSF2
The Distribution of Activation Markers and Selectins on Peripheral T Lymphocytes in Preeclampsia.
Mediators of inflammation | 2017-01-01 | PMID 28555090
Bajnok Anna, Ivanova Maria, Rigó János and 1 more
The ATP-Dependent Protease ClpP Inhibits Biofilm Formation by Regulating Agr and Cell Wall Hydrolase Sle1 in Staphylococcus aureus.
Frontiers in cellular and infection microbiology | 2017-01-01 | PMID 28555174
Liu Qian, Wang Xing, Qin Juanxiu and 7 more
A Turkish case of galactosialidosis with a new homozygous mutation in CTSA gene.
Metabolic brain disease | 2017-08-01 | PMID 28555253
Kartal Ayşe, Aydın Kürşad
Genes: CTSA
qRfg3, a novel quantitative resistance locus against Gibberella stalk rot in maize.
TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik | 2017-08-01 | PMID 28555262
Ma Chuanyu, Ma Xuena, Yao Lishan and 4 more
Genetic diagnostics of inherited aortic diseases : Medical strategy analysis.
Herz | 2017-08-01 | PMID 28555287
von Kodolitsch Y, Kutsche K
[Congenital disorders of lipoprotein metabolism].
Herz | 2017-08-01 | PMID 28555288
März W, Grammer T B, Delgado G and 1 more
Genes: APOB, PCSK9, LDLR, STAP1
A mutated dph3 gene causes sensitivity of Schizosaccharomyces pombe cells to cytotoxic agents.
Current genetics | 2017-12-01 | PMID 28555368
Villahermosa Desirée, Knapp Karen, Fleck Oliver
Genetics of rheumatoid arthritis susceptibility, severity, and treatment response.
Seminars in immunopathology | 2017-06-01 | PMID 28555384
Viatte Sebastien, Barton Anne
Cytokine storm and sepsis disease pathogenesis.
Seminars in immunopathology | 2017-07-01 | PMID 28555385
Chousterman Benjamin G, Swirski Filip K, Weber Georg F
Emerging multidrug-resistant Bengal Bay clone ST772-MRSA-V in Norway: molecular epidemiology 2004-2014.
European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology | 2017-10-01 | PMID 28555401
Blomfeldt A, Larssen K W, Moghen A and 4 more
Dissemination of bla OXA-370 gene among several Enterobacteriaceae species in Brazil.
European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology | 2017-10-01 | PMID 28555403
Magagnin C M, Rozales F P, Antochevis L and 5 more
Genes: VIM
Investigation of previously implicated genetic variants in chronic tic disorders: a transmission disequilibrium test approach.
European archives of psychiatry and clinical neuroscience | 2018-04-01 | PMID 28555406
Abdulkadir Mohamed, Londono Douglas, Gordon Derek and 46 more
Genes: PICALM, TBCD, TPH2
Epigenetic dysregulation of hematopoietic stem cells and preleukemic state.
International journal of hematology | 2017-07-01 | PMID 28555413
Kunimoto Hiroyoshi, Nakajima Hideaki
Genes: ASXL1, TET2
Germline ETV6 mutations and predisposition to hematological malignancies.
International journal of hematology | 2017-08-01 | PMID 28555414
Feurstein Simone, Godley Lucy A
Genes: ETV6, RUNX1
[A phenotypic description of 26 patients with Ritscher-Schinzel syndrome (cranio-cerebello-cardiac dysplasia or 3C syndrome)].
Revista de neurologia | 2017-06-01 | PMID 28555453
Pira-Paredes S M, Montoya-Villada J H, Franco-Restrepo J L and 2 more
Statin intolerance in heterozygous familial hypercolesterolemia with cardiovascular disease: After PCSK-9 antibodies what else?
European journal of preventive cardiology | 2017-09-01 | PMID 28555526
Sbrana Francesco, Dal Pino Beatrice, Bigazzi Federico and 14 more
Genes: PCSK9
Family environments and leukocyte transcriptome indicators of a proinflammatory phenotype in children and parents.
Development and psychopathology | 2018-02-01 | PMID 28555535
Robles Theodore F, Repetti Rena L, Reynolds Bridget M and 3 more
Low Birthweight Increases the Likelihood of Severe Steatosis in Pediatric Non-Alcoholic Fatty Liver Disease.
The American journal of gastroenterology | 2017-08-01 | PMID 28555633
Bugianesi Elisabetta, Bizzarri Carla, Rosso Chiara and 9 more
Genes: AGA, PNPLA3
Pyk2 modulates hippocampal excitatory synapses and contributes to cognitive deficits in a Huntington's disease model.
Nature communications | 2017-05-30 | PMID 28555636
Giralt Albert, Brito Veronica, Chevy Quentin and 9 more
Genes: PSD
Clonally stable Vκ allelic choice instructs Igκ repertoire.
Nature communications | 2017-05-30 | PMID 28555639
Levin-Klein Rena, Fraenkel Shira, Lichtenstein Michal and 7 more
A promoter-proximal transcript targeted by genetic polymorphism controls E-cadherin silencing in human cancers.
Nature communications | 2017-05-30 | PMID 28555645
Pisignano Giuseppina, Napoli Sara, Magistri Marco and 15 more
Associating cellular epigenetic models with human phenotypes.
Nature reviews. Genetics | 2017-07-01 | PMID 28555657
Lappalainen Tuuli, Greally John M
Human Y-chromosome variation in the genome-sequencing era.
Nature reviews. Genetics | 2017-08-01 | PMID 28555659
Jobling Mark A, Tyler-Smith Chris
MiCASA is a new method for quantifying cellular organization.
Nature communications | 2017-05-30 | PMID 28555660
Sornborger Andrew, Li Jie, Timmons Cullen and 4 more
Concurrent mood and anxiety disorders are associated with pharmacoresistant seizures in patients with MTLE.
Epilepsia | 2017-07-01 | PMID 28555776
Nogueira Mateus H, Yasuda Clarissa L, Coan Ana C and 2 more
Intraspecific variation in growth rate is a poor predictor of fitness for reef corals.
Ecology | 2017-08-01 | PMID 28555884
Edmunds Peter J
Functional severity of CLCNKB mutations correlates with phenotypes in patients with classic Bartter's syndrome.
The Journal of physiology | 2017-08-15 | PMID 28555925
Cheng Chih-Jen, Lo Yi-Fen, Chen Jen-Chi and 2 more
Genes: CLCNKB
Soluble activin receptor type IIB decoy receptor differentially impacts murine osteogenesis imperfecta muscle function.
Muscle & nerve | 2018-02-01 | PMID 28555931
Jeong Youngjae, Daghlas Salah A, Kahveci Alp S and 6 more
Altered molecular profile in thyroid cancers from patients affected by the Three Mile Island nuclear accident.
The Laryngoscope | 2017-07-01 | PMID 28555940
Goldenberg David, Russo Mariano, Houser Kenneth and 7 more
Genes: BRAF
Roaming of dogs in remote Indigenous communities in northern Australia and potential interaction between community and wild dogs.
Australian veterinary journal | 2017-06-01 | PMID 28555947
Bombara C, Dürr S, Gongora J and 1 more
Hereditary progressive mucinous histiocytosis: 3 different phenotypes in 3 family members.
Journal of cutaneous pathology | 2017-09-01 | PMID 28556021
Requena Celia, Requena Luis, Traves Victor and 1 more
Diabetic macular oedema: clinical risk factors and emerging genetic influences.
Clinical & experimental optometry | 2017-11-01 | PMID 28556097
Liu Ebony, Craig Jamie E, Burdon Kathryn
Decreased plasma β-amyloid in the Alzheimer's disease APP A673T variant carriers.
Annals of neurology | 2017-07-01 | PMID 28556232
Martiskainen Henna, Herukka Sanna-Kaisa, Stančáková Alena and 5 more
Genes: APP, ABCA7
Cerebral compensation during motor function in Friedreich ataxia: The IMAGE-FRDA study.
Movement disorders : official journal of the Movement Disorder Society | 2017-08-01 | PMID 28556242
Harding Ian H, Corben Louise A, Delatycki Martin B and 4 more
Cacna1g is a genetic modifier of epilepsy in a mouse model of Dravet syndrome.
Epilepsia | 2017-08-01 | PMID 28556246
Calhoun Jeffrey D, Hawkins Nicole A, Zachwieja Nicole J and 1 more
Nitric oxide induces monosaccharide accumulation through enzyme S-nitrosylation.
Plant, cell & environment | 2017-09-01 | PMID 28556250
Zhang Zhong-Wei, Luo Sha, Zhang Gong-Chang and 14 more
Incidence of nonamyloidogenic mutations in the transthyretin gene in patients with autonomic and small fiber neuropathy.
Muscle & nerve | 2018-01-01 | PMID 28556268
Levine Todd D, Bland Ruth J
Genes: TTR, SFN
SUV2, which encodes an ATR-related cell cycle checkpoint and putative plant ATRIP, is required for aluminium-dependent root growth inhibition in Arabidopsis.
Plant, cell & environment | 2017-09-01 | PMID 28556304
Sjogren Caroline A, Larsen Paul B
Genes: ATR, ATRIP
Identification of a functional enhancer variant within the chronic pancreatitis-associated SPINK1 c.101A>G (p.Asn34Ser)-containing haplotype.
Human mutation | 2017-08-01 | PMID 28556356
Boulling Arnaud, Masson Emmanuelle, Zou Wen-Bin and 11 more
Genes: SPINK1
Association of cytochrome P450 1B1 haplotypes with head and neck cancer risk.
Environmental and molecular mutagenesis | 2017-07-01 | PMID 28556360
Katiyar Tridiv, Maurya Shailendra S, Hasan Feza and 6 more
The genetic landscape of familial congenital hydrocephalus.
Annals of neurology | 2017-06-01 | PMID 28556411
Shaheen Ranad, Sebai Mohammed Adeeb, Patel Nisha and 26 more
Genes: MPDZ, EML1
Neuregulin 3 and its roles in schizophrenia risk and presentation.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics | 2018-03-01 | PMID 28556469
Avramopoulos Dimitrios
Genes: NRG3, NRG1
Describing mate preference functions and other function-valued traits.
Journal of evolutionary biology | 2017-09-01 | PMID 28556474
Kilmer J T, Fowler-Finn K D, Gray D A and 4 more
Factors associated with risk of central nervous system relapse in patients with non-core binding factor acute myeloid leukemia.
American journal of hematology | 2017-09-01 | PMID 28556489
Jabbour Elias, Guastad Daver Naval, Short Nicholas James and 16 more
Genes: FLT3
A genome-wide quantitative trait locus (QTL) linkage scan of NEO personality factors in Latino families segregating bipolar disorder.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics | 2017-10-01 | PMID 28556497
Lee Byung Dae, Gonzalez Suzanne, Villa Erika and 10 more
Genes: BPI
A state-wide initiative to promote genetic testing in an underserved population.
Cancer medicine | 2017-07-01 | PMID 28556546
Underhill Meghan L, Blonquist Traci M, Habin Karleen and 5 more