Insights into modifiable risk factors of cholelithiasis: A Mendelian randomization study.
Hepatology (Baltimore, Md.) | 2022-04-01 | PMID 34624136
Chen Lanlan, Yang Hongqun, Li Haitao and 3 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.
Semantic proximity supports literature exploration. It does not establish scientific or clinical evidence.
Publications
Page 8719 of 10600
The N-terminal domain of SARS-CoV-2 nsp1 plays key roles in suppression of cellular gene expression and preservation of viral gene expression.
Cell reports | 2021-10-19 | PMID 34624207
Mendez Aaron S, Ly Michael, González-Sánchez Angélica M and 4 more
Phenotypic characterization of Cdkl5-knockdown neurons establishes elongated cilia as a functional assay for CDKL5 Deficiency Disorder.
Neuroscience research | 2022-03-01 | PMID 34624412
Di Nardo Alessia, Rühmkorf Alina, Award Patricia and 3 more
Genes: CDKL5
Translocator Protein Regulate Polarization Phenotype Transformation of Microglia after Cerebral Ischemia-reperfusion Injury.
Neuroscience | 2022-01-01 | PMID 34624453
Yusuying Shadamu, Yusuyin Shalayiding, Cheng Xiaojiang
Association and functional significance of genetic variants present in regulatory elements of SERPINB5 gene in gallbladder cancer.
Gene | 2022-01-15 | PMID 34624458
Sinha Kirti Kumari, Vinay J, Parida Suryakant and 2 more
Discovery and optimization of covalent EGFR T790M/L858R mutant inhibitors.
Bioorganic & medicinal chemistry letters | 2021-11-15 | PMID 34624491
Hoogenboom Niels, Demont Dennis, de Zwart Edwin and 5 more
Long-term adjustment of hepatic lipid metabolism after chronic stress and the role of FGF21.
Biochimica et biophysica acta. Molecular basis of disease | 2022-01-01 | PMID 34624498
Dille Matthias, Nikolic Aleksandra, Wahlers Natalie and 9 more
Common Postzygotic Mutational Signatures in Healthy Adult Tissues Related to Embryonic Hypoxia.
Genomics, proteomics & bioinformatics | 2022-02-01 | PMID 34624550
Hong Yaqiang, Zhang Dake, Zhou Xiangtian and 22 more
Intermittent macrothrombocytopenia in a novel patient with Takenouchi-Kosaki syndrome and review of literature.
European journal of medical genetics | 2021-12-01 | PMID 34624555
Santoro Claudia, Gaudino Giuseppina, Torella Annalaura and 5 more
Clinical presentation and analysis of genotype-phenotype correlations in patients with malignant infantile osteopetrosis.
Bone | 2022-01-01 | PMID 34624559
Even-Or Ehud, Schiesel Gali, Simanovsky Natalia and 5 more
The combination of aging and chronic kidney disease leads to an exacerbated cortical porosity phenotype.
Bone | 2022-01-01 | PMID 34624561
Tippen Samantha P, Metzger Corinne E, Swallow Elizabeth A and 3 more
Activation of the TGF-β1/Smad signaling by KIF2C contributes to the malignant phenotype of thyroid carcinoma cells.
Tissue & cell | 2021-12-01 | PMID 34624565
Lin Qiuyu, Qi Qianle, Hou Sen and 4 more
Quantile-specific heritability of monocyte chemoattractant protein-1, and relevance to rs1024611-disease interactions.
Cytokine | 2022-01-01 | PMID 34624603
Williams Paul T
A case of Maffucci syndrome with a buccal hemangioma harboring a mutation in IDH1.
Oral oncology | 2021-11-01 | PMID 34624834
Ichimura Norihisa, Yamamoto Noriyuki, Toyama Naoto and 1 more
Absence of the RNF213 p.R4810K variant may indicate a severe form of pediatric moyamoya disease in Japanese patients.
Journal of neurosurgery. Pediatrics | 2022-01-01 | PMID 34624841
Hara Shoko, Mukawa Maki, Akagawa Hiroyuki and 6 more
Comparative physiological and transcriptomic analyses reveal ascorbate and glutathione coregulation of cadmium toxicity resistance in wheat genotypes.
BMC plant biology | 2021-10-08 | PMID 34625028
Zhang Tao, Xiao Jingui, Zhao Yongsheng and 7 more
Physiological and transcriptome analysis of Magnolia denudata leaf buds during long-term cold acclimation.
BMC plant biology | 2021-10-08 | PMID 34625030
Wu Kunjing, Duan Xiaojing, Zhu Zhonglong and 4 more
Whole genome copy number analyses reveal a highly aberrant genome in TP53 mutant lung adenocarcinoma tumors.
BMC cancer | 2021-10-09 | PMID 34625038
Bjaanæs Maria Moksnes, Nilsen Gro, Halvorsen Ann Rita and 6 more
Component of oligomeric Golgi complex 1 deficiency leads to hypoglycemia: a case report and literature review.
BMC pediatrics | 2021-10-08 | PMID 34625039
Huang Yizhou, Dai Han, Yang Gangyi and 3 more
Rare single nucleotide variants in COL5A1 promoter do not play a major role in keratoconus susceptibility associated with rs1536482.
BMC ophthalmology | 2021-10-08 | PMID 34625056
Skorodumova Liubov O, Belodedova Alexandra V, Sharova Elena I and 11 more
The potential risk of enzootic Trypanosoma cruzi transmission inside four training and re-training military battalions (BITER) in Colombia.
Parasites & vectors | 2021-10-09 | PMID 34625109
Cantillo-Barraza Omar, Torres Jeffer, Hernández Carolina and 8 more
JAK-STAT signaling in human disease: From genetic syndromes to clinical inhibition.
The Journal of allergy and clinical immunology | 2021-10-01 | PMID 34625141
Luo Yiming, Alexander Madison, Gadina Massimo and 3 more
The association between interleukin-6 promoter polymorphisms and rheumatoid arthritis by ethnicity: A meta-analysis of 33 studies.
Reumatologia clinica | 2021-10-01 | PMID 34625147
Pacheco-Soto Blanca T, Porchia Leonardo M, Lara-Vazquez William C and 3 more
PTEN mutations in autism spectrum disorder and congenital hydrocephalus: developmental pleiotropy and therapeutic targets.
Trends in neurosciences | 2021-12-01 | PMID 34625286
DeSpenza Tyrone, Carlson Marina, Panchagnula Shreyas and 12 more
Definitive roles of TOMM40-APOE-APOC1 variants in the Alzheimer's risk.
Neurobiology of aging | 2022-02-01 | PMID 34625307
Kulminski Alexander M, Philipp Ian, Shu Leonardo and 1 more
Diagnostic challenges and disease management in patients with a mild Zellweger spectrum disorder phenotype.
Molecular genetics and metabolism | 2021-11-01 | PMID 34625341
Enns Gregory M, Ammous Zineb, Himes Ryan W and 4 more
Adult rheumatologic features, treatment and complications of X-linked hypophosphatemia.
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie | 2021-10-01 | PMID 34625379
Salcion Axelle, Herrou Julia, Briot Karine
Novel Models of Genetic Education and Testing for Pancreatic Cancer Interception: Preliminary Results from the GENERATE Study.
Cancer prevention research (Philadelphia, Pa.) | 2021-11-01 | PMID 34625409
Furniss C Sloane, Yurgelun Matthew B, Ukaegbu Chinedu and 25 more
The Mutational Signature Comprehensive Analysis Toolkit (musicatk) for the Discovery, Prediction, and Exploration of Mutational Signatures.
Cancer research | 2021-12-01 | PMID 34625425
Chevalier Aaron, Yang Shiyi, Khurshid Zainab and 5 more
Molecular Characteristics of Repotrectinib That Enable Potent Inhibition of TRK Fusion Proteins and Resistant Mutations.
Molecular cancer therapeutics | 2021-12-01 | PMID 34625502
Murray Brion W, Rogers Evan, Zhai Dayong and 10 more
Neonatal-onset mitochondrial disease: clinical features, molecular diagnosis and prognosis.
Archives of disease in childhood. Fetal and neonatal edition | 2022-05-01 | PMID 34625524
Ebihara Tomohiro, Nagatomo Taro, Sugiyama Yohei and 17 more
A Review of Phosphocreatine 3 Kinase δ Subtype (PI3Kδ) and Its Inhibitors in Malignancy.
Medical science monitor : international medical journal of experimental and clinical research | 2021-10-09 | PMID 34625526
Xiang Qiong, Dong Shuai, Li Xian-Hui
Alpelisib combination treatment as novel targeted therapy against hepatocellular carcinoma.
Cell death & disease | 2021-10-08 | PMID 34625531
Xu Hongwei, Chen Kefei, Shang Runze and 8 more
Genes: PIK3CA, CDK4
Dysregulated APOBEC3G causes DNA damage and promotes genomic instability in multiple myeloma.
Blood cancer journal | 2021-10-08 | PMID 34625538
Talluri Srikanth, Samur Mehmet K, Buon Leutz and 6 more
Cryo-EM structures of the ABCA4 importer reveal mechanisms underlying substrate binding and Stargardt disease.
Nature communications | 2021-10-08 | PMID 34625547
Scortecci Jessica Fernandes, Molday Laurie L, Curtis Susan B and 4 more
Genes: ABCA4, ECD
Human cell based directed evolution of adenine base editors with improved efficiency.
Nature communications | 2021-10-08 | PMID 34625552
Fu Junhao, Li Qing, Liu Xiaoyu and 9 more
BRAF mutations may identify a clinically distinct subset of glioblastoma.
Scientific reports | 2021-10-08 | PMID 34625582
McNulty Samantha N, Schwetye Katherine E, Ferguson Cole and 7 more
GAS5 rs2067079 and miR-137 rs1625579 functional SNPs and risk of chronic hepatitis B virus infection among Egyptian patients.
Scientific reports | 2021-10-08 | PMID 34625583
Mahmoud Rania H, Hefzy Enas Mamdouh, Shaker Olfat G and 7 more
Subventricular zone involvement is associated with worse outcome in glioma WHO grade 2 depending on molecular markers.
Scientific reports | 2021-10-08 | PMID 34625590
Karschnia Philipp, Weller Jonathan, Blobner Jens and 9 more
SNP markers reveal relationships between fruit paternity, fruit quality and distance from a cross-pollen source in avocado orchards.
Scientific reports | 2021-10-08 | PMID 34625603
Kämper Wiebke, Ogbourne Steven M, Hawkes David and 1 more
Clinical phenotypes from fatal cases of acute respiratory distress syndrome caused by pneumonia.
Scientific reports | 2021-10-08 | PMID 34625618
Ichikado Kazuya, Kawamura Kodai, Johkoh Takeshi and 17 more
Genetic polymorphisms of BDNF on cognitive functions in drug-naive first episode patients with schizophrenia.
Scientific reports | 2021-10-08 | PMID 34625629
Su Xiuru, Qiao Limin, Liu Qing and 4 more
Distribution of bacteriocin genes in the lineages of Lactiplantibacillus plantarum.
Scientific reports | 2021-10-08 | PMID 34625657
Choi Sungmi, Baek Min-Gyung, Chung Myung-Jun and 2 more
Calcium-dependent signalling in B-cell lymphomas.
Oncogene | 2021-11-01 | PMID 34625709
Berditchevski Fedor, Fennell Eanna, Murray Paul G
RPPA-based proteomics recognizes distinct epigenetic signatures in chronic lymphocytic leukemia with clinical consequences.
Leukemia | 2022-03-01 | PMID 34625713
van Dijk Anneke D, Griffen Ti'ara L, Qiu Yihua H and 9 more
Association between lung compliance phenotypes and mortality in COVID-19 patients with acute respiratory distress syndrome.
Annals of the Academy of Medicine, Singapore | 2021-09-01 | PMID 34625756
Puah Ser Hon, Cove Matthew Edward, Phua Jason and 13 more
Phenotypic presentation of PCOS with respect to BMI in a north Indian population.
La Clinica terapeutica | 2021-09-29 | PMID 34625775
Kaur R, Kaur M, Suri V
Frequent mutations of FBXO11 highlight BCL6 as a therapeutic target in Burkitt lymphoma.
Blood advances | 2021-12-14 | PMID 34625792
Pighi Chiara, Cheong Taek-Chin, Compagno Mara and 23 more
[Analysis of genetic variant in a child with autosomal recessive Alport syndrome].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2021-10-10 | PMID 34625929
Chen Lan, Zhang Yiyan, Lin Weisheng
[Genetic diagnosis of a pedigree affected with Usher syndrome type 1D/F].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2021-10-10 | PMID 34625930
Kang Hongfei, Zhao Kaihui, Kong Xiangdong
[Clinical characteristics and therapeutic effect of TP53 variant in patients with acute leukemia].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2021-10-10 | PMID 34625931
Mi Ruihua, Guo Zhen, Liu Wen and 5 more
[Analysis of two novel variants of FUT1 gene in a Chinese family with para-Bombay phenotype].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2021-10-10 | PMID 34625943
Zhang Kunlian, Lin Fengqiu, Li Xiaofeng and 2 more
Identifying Potential Therapeutic Applications and Diagnostic Harms of Increased Bilirubin Concentrations: A Clinical and Genetic Approach.
Clinical pharmacology and therapeutics | 2022-02-01 | PMID 34625956
Zanussi Jacy T, Zhao Juan, Dorn Chad A and 6 more
Global molecular prevalence and genotype distribution of Sapovirus in children with gastrointestinal complications: A systematic review and meta-analysis.
Reviews in medical virology | 2022-05-01 | PMID 34626019
Razizadeh Mohammad Hossein, Khatami Alireza, Zarei Mohammad
Little evidence for genetic variation associated with susceptibility to sea star wasting syndrome in the keystone species Pisaster ochraceus.
Molecular ecology | 2022-01-01 | PMID 34626020
Burton Andrea R, Gravem Sarah A, Barreto Felipe S
Aberrant expression of MYD88 via RNA-controlling CNOT4 and EXOSC3 in colonic mucosa impacts generation of colonic cancer.
Cancer science | 2021-12-01 | PMID 34626022
Tsuda Masumi, Noguchi Misa, Kurai Tsuyoshi and 8 more
F9 missense mutations impairing factor IX activation are associated with pleiotropic plasma phenotypes.
Journal of thrombosis and haemostasis : JTH | 2022-01-01 | PMID 34626083
Branchini Alessio, Morfini Massimo, Lunghi Barbara and 12 more
Identification of the novel HLA-A*30:181 allele by next-generation sequencing.
HLA | 2022-02-01 | PMID 34626087
Troiano Maria, Giustiniani Paola, Di Luzio Andrea and 2 more
Characterization of the novel HLA-B*52:01:01:18 allele in a West Indian individual.
HLA | 2022-02-01 | PMID 34626094
Phuntsok Tenzin, D'Silva Selma Z, Tambe Manisha and 2 more
Detecting Selection in Multiple Populations by Modeling Ancestral Admixture Components.
Molecular biology and evolution | 2022-01-07 | PMID 34626111
Cheng Jade Yu, Stern Aaron J, Racimo Fernando and 1 more
Genetic polymorphism of bovine beta-casein gene in Japanese dairy farm herds.
Animal science journal = Nihon chikusan Gakkaiho | 2021-01-01 | PMID 34626147
Yamada Asaha, Sugimura Miyu, Kuramoto Takashi
Effect of steroid hormone receptor gene variants PROGINS (Alu insertion) and PGR C/T (rs1042839) as a risk factor for recurrent pregnancy loss in Kashmiri population (North India).
The journal of obstetrics and gynaecology research | 2021-12-01 | PMID 34626148
Khan Nebela, Zargar Mahrukh Hameed, Ahmed Rehana and 4 more
Sexual size and shape dimorphism in Turkish common toads (Bufo bufo Linnaeus 1758).
Anatomical record (Hoboken, N.J. : 2007) | 2022-06-01 | PMID 34626158
Dursun Cantekin, Gül Serkan, Özdemir Nurhayat
Pollen-specific gene SKU5-SIMILAR 13 enhances growth of pollen tubes in the transmitting tract in Arabidopsis.
Journal of experimental botany | 2022-01-27 | PMID 34626184
Zhang Ming Jun, Zhao Tian Yi, Ouyang Xiu Ke and 3 more
Circulating Cell-Free DNA Yield and Circulating-Tumor DNA Quantity from Liquid Biopsies of 12 139 Cancer Patients.
Clinical chemistry | 2021-11-01 | PMID 34626187
Huang Richard S P, Xiao Jinpeng, Pavlick Dean C and 17 more
Uterine cellular leiomyomas are characterized by common HMGA2 aberrations, followed by chromosome 1p deletion and MED12 mutation: morphological, molecular, and immunohistochemical study of 52 cases.
Virchows Archiv : an international journal of pathology | 2022-02-01 | PMID 34626221
Dundr Pavel, Gregová Mária, Hojný Jan and 10 more
Gliomas in children and adolescents: investigation of molecular alterations with a potential prognostic and therapeutic impact.
Journal of cancer research and clinical oncology | 2022-01-01 | PMID 34626238
Cabral de Carvalho Corrêa Débora, Tesser-Gamba Francine, Dias Oliveira Indhira and 6 more
Association between alcohol and bone mineral density in a Mendelian randomization study: the Dong-gu study.
Journal of bone and mineral metabolism | 2022-01-01 | PMID 34626249
Choi Chang Kyun, Kweon Sun-Seog, Lee Young-Hoon and 5 more
Genetic study of a patient with congenital central hypoventilation syndrome in Iran: a case report.
Molecular biology reports | 2021-12-01 | PMID 34626313
Khorasanian Reihaneh, Mojbafan Marzieh, Khosravi Nastaran
Advances in Diagnosis and Risk Stratification of Acute Myeloid Leukemia and Myelodysplastic Syndromes.
Cancer treatment and research | 2021-01-01 | PMID 34626352
Pillai Raju K, Afkhami Michelle
Genetics and Diagnostic Approach to Lymphoblastic Leukemia/Lymphoma.
Cancer treatment and research | 2021-01-01 | PMID 34626353
Afkhami Michelle, Ally Feras, Pullarkat Vinod and 1 more
Biology and Current Treatment of Myeloproliferative Neoplasms.
Cancer treatment and research | 2021-01-01 | PMID 34626360
Ali Haris, Pullarkat Vinod, Snyder David
Molecular Genetic Techniques for the Proteoglycan Functions in Drosophila.
Methods in molecular biology (Clifton, N.J.) | 2022-01-01 | PMID 34626396
Bowden Nanako, Takemura Masahiko, Nakato Hiroshi
Conservation and coevolution determine evolvability of different classes of disordered residues in human intrinsically disordered proteins.
Proteins | 2022-03-01 | PMID 34626492
Basu Sushmita, Bahadur Ranjit Prasad
SPRED2 loss-of-function causes a recessive Noonan syndrome-like phenotype.
American journal of human genetics | 2021-11-04 | PMID 34626534
Motta Marialetizia, Fasano Giulia, Gredy Sina and 30 more
Revisiting the out of Africa event with a deep-learning approach.
American journal of human genetics | 2021-11-04 | PMID 34626535
Montinaro Francesco, Pankratov Vasili, Yelmen Burak and 2 more
Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, epilepsy, and hearing loss.
American journal of human genetics | 2021-10-07 | PMID 34626583
Richard Elodie M, Bakhtiari Somayeh, Marsh Ashley P L and 102 more
Asthma-COPD Overlap: What Are the Important Questions?
Chest | 2022-02-01 | PMID 34626594
Leung Clarus, Sin Don D
Novel mutations associated with carnitine-acylcarnitine translocase and carnitine palmitoyl transferase 2 deficiencies in Malaysia.
Clinical biochemistry | 2021-12-01 | PMID 34626609
Habib Anasufiza, Azize Nor Azimah Abdul, Rahman Salina Abd and 8 more
Strongwellsea crypta (Entomophthorales: Entomophthoraceae), a new species infecting Botanophila fugax (Diptera: Anthomyiidae).
Journal of invertebrate pathology | 2021-11-01 | PMID 34626615
Eilenberg Jørgen, Michelsen Verner, Jensen Annette Bruun and 1 more
New therapeutic approaches to Parkinson's disease targeting GBA, LRRK2 and Parkin.
Neuropharmacology | 2022-01-01 | PMID 34626666
Senkevich Konstantin, Rudakou Uladzislau, Gan-Or Ziv
Novel heterozygous mutations in the otogelin-like (OTOGL) gene in a child with bilateral mild nonsyndromic sensorineural hearing loss.
Gene | 2022-01-15 | PMID 34626719
Pan Chen, Li Jun, Wang Shixin and 3 more
Integrative analysis of transcriptome-wide association study and mRNA expression profile identified candidate genes and pathways associated with aortic aneurysm and dissection.
Gene | 2022-01-15 | PMID 34626721
Zhang Yiran, Li Lin, Ma Liang
High ORAI3 expression correlates with good prognosis in human muscle-invasive bladder cancer.
Gene | 2022-01-15 | PMID 34626722
Yan Jing, Yu Wei, Lu Chang and 5 more
Simultaneous detection and genetic characterization of porcine circovirus 2 and 4 in Henan province of China.
Gene | 2022-01-15 | PMID 34626723
Xu Tong, Hou Cheng-Yao, Zhang Yuan-Hang and 4 more
Segregation of nuclear and membrane-initiated actions of estrogen receptor using genetically modified animals and pharmacological tools.
Molecular and cellular endocrinology | 2022-01-01 | PMID 34626731
Adlanmerini Marine, Fontaine Coralie, Gourdy Pierre and 2 more
Evaluation of divalent metal transporter 1 (DMT1) (rs224589) polymorphism on blood lead levels of occupationally exposed individuals.
Toxicology letters | 2021-12-15 | PMID 34626817
Mani Monica Shirley, Dsouza Venzil Lavie, Dsouza Herman Sunil
IMpower150 Final Exploratory Analyses for Atezolizumab Plus Bevacizumab and Chemotherapy in Key NSCLC Patient Subgroups With EGFR Mutations or Metastases in the Liver or Brain.
Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer | 2022-02-01 | PMID 34626838
Nogami Naoyuki, Barlesi Fabrice, Socinski Mark A and 20 more
Defective Lipid Droplet-Lysosome Interaction Causes Fatty Liver Disease as Evidenced by Human Mutations in TMEM199 and CCDC115.
Cellular and molecular gastroenterology and hepatology | 2022-01-01 | PMID 34626841
Larsen Lars E, van den Boogert Marjolein A W, Rios-Ocampo Wilson A and 16 more
Generation of the induced pluripotent stem cell line (NCKDi004-A) from a 17-year-old patient with Alport syndrome carrying a homozygous mutation in COL4A3 gene.
Stem cell research | 2021-10-01 | PMID 34626894
Wu Hangdi, Wang Gang, Gao Erzhi and 4 more
Evaluation of candidate point mutation of Kisspeptin 1 gene associated with litter size in Indian Goat breeds and its effect on transcription factor binding sites.
Domestic animal endocrinology | 2022-01-01 | PMID 34626930
Jeet Vikram, Magotra Ankit, Bangar Y C and 4 more
Soft substrate stiffness modifies corneal epithelial stem cell phenotype through hippo-YAP/notch pathway crosstalk.
Medical hypotheses | 2021-11-01 | PMID 34627046
Pu Qi, Ma Qian, Li Jing and 2 more
Genetic contribution and functional impairment of inflammasome in sickle cell disease.
Cytokine | 2022-01-01 | PMID 34627079
de Freitas Dutra Valéria, Leal Vinícius Nunes Cordeiro, Fernandes Fernanda Pereira and 3 more
Ovarian reserve of women with and without BRCA pathogenic variants: A systematic review and meta-analysis.
Breast (Edinburgh, Scotland) | 2021-12-01 | PMID 34627117
Gasparri Maria Luisa, Di Micco Rosa, Zuber Veronica and 9 more
Genetically predicted insomnia and lung cancer risk: a Mendelian randomization study.
Sleep medicine | 2021-11-01 | PMID 34627121
Huo Zhenyu, Ge Fan, Li Caichen and 11 more
Comparison of sequencing data processing pipelines and application to underrepresented African human populations.
BMC bioinformatics | 2021-10-09 | PMID 34627144
Breton Gwenna, Johansson Anna C V, Sjödin Per and 2 more
A systematic review of common genetic variation and biological pathways in autism spectrum disorder.
BMC neuroscience | 2021-10-09 | PMID 34627165
Rodriguez-Gomez Diego Alejandro, Garcia-Guaqueta Danna Paola, Charry-Sánchez Jesús David and 4 more
Hyaline fibromatosis syndrome: a case presenting with gingival enlargement as the only clinical manifestation and a report of two new mutations in the ANTXR2 gene.
BMC oral health | 2021-10-09 | PMID 34627224
Liu Yiying, Zeng Xin, Ding Yi and 2 more
Copy number variation analysis in Chinese children with complete atrioventricular canal and single ventricle.
BMC medical genomics | 2021-10-09 | PMID 34627233
Zhang Xingyu, Wang Bo, You Guoling and 4 more
Genetic variation of Plasmodium falciparum histidine-rich protein 2 and 3 in Assosa zone, Ethiopia: its impact on the performance of malaria rapid diagnostic tests.
Malaria journal | 2021-10-09 | PMID 34627242
Alemayehu Gezahegn Solomon, Messele Alebachew, Blackburn Kayla and 4 more