A novel and cost-efficient allele-specific PCR method for multiple SNP genotyping in a single run.
Analytica chimica acta | 2022-10-09 | PMID 36156224
He Qidi, Hu Ou, Chen Meng 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.
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Publications
Page 9006 of 10600
Long response to immune checkpoint inhibitors in metastatic NSCLC despite EGFR germline mutation. A case report.
Lung cancer (Amsterdam, Netherlands) | 2022-12-01 | PMID 36156246
Trabelsi Grati Olfa, Zemoura Leila, Nhy Caroline and 6 more
VPS13D-based disease: Expansion of the clinical phenotype in two brothers and mutation diversity in the Turkish population.
Revue neurologique | 2022-11-01 | PMID 36156252
Öztop-Çakmak Ö, Şimşir G, Tekgül Ş and 7 more
Ethnic differences between Asians and non-Asians in clustering-based phenotype classification of adult-onset diabetes mellitus: A systematic narrative review.
Primary care diabetes | 2022-12-01 | PMID 36156263
Varghese Jithin Sam, Narayan K M Venkat
Melanoma-specific survival before and after inclusion in a familial melanoma dermatologic surveillance program in CDKN2A mutation carriers and non-carriers.
Journal of the European Academy of Dermatology and Venereology : JEADV | 2023-02-01 | PMID 36156317
Pissa Maria, Lapins Jan, Sköldmark Christina and 1 more
Prevalence and breakdown of non-small cell lung cancer BRAF driver mutations in a large UK cohort.
Lung cancer (Amsterdam, Netherlands) | 2022-11-01 | PMID 36156323
Lim Guan Hui Tricia, Balbi Kevin Jon, Poskitt Benjamin and 2 more
MCU controls melanoma progression through a redox-controlled phenotype switch.
EMBO reports | 2022-11-07 | PMID 36156348
Stejerean-Todoran Ioana, Zimmermann Katharina, Gibhardt Christine S and 27 more
Paternal genetic structure of the Qiang ethnic group in China revealed by high-resolution Y-chromosome STRs and SNPs.
Forensic science international. Genetics | 2022-11-01 | PMID 36156385
Song Mengyuan, Wang Zefei, Lyu Qiang and 10 more
Reduced resource utilization with early use of next-generation sequencing in rare genetic diseases in an Asian cohort.
American journal of medical genetics. Part A | 2022-12-01 | PMID 36156406
Nazeha Nuraini, Koh Ai Ling, Kam Sylvia and 4 more
Structural topological analysis of spike proteins of SARS-CoV-2 variants of concern highlight distinctive amino acid substitution patterns.
European journal of cell biology | 2000-01-01 | PMID 36156414
Peisahovics Filips, Rohaim Mohammed A, Munir Muhammad
Deletion of 11q24.2-qter in a male child with cleft lip and palate: an atypical feature of Jacobsen syndrome.
Journal of genetics | 2022-01-01 | PMID 36156508
Wang Jundao, Zhao Tianli, Tan Zhiping and 4 more
Cross-GWAS coherence test at the gene and pathway level.
PLoS computational biology | 2022-09-01 | PMID 36156592
Krefl Daniel, Bergmann Sven
Idiopathic infantile hypercalcemia in children with chronic kidney disease due to kidney hypodysplasia.
Pediatric nephrology (Berlin, Germany) | 2023-04-01 | PMID 36156733
Gurevich Evgenia, Borovitz Yael, Levi Shelli and 2 more
Childhood asthma and type 1 diabetes mellitus: A meta-analysis and bidirectional Mendelian randomization study.
Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology | 2022-09-01 | PMID 36156818
Xie Junyang, Chen Gui, Liang Tianhao and 9 more
Afatinib Targeted Therapy Affects the Immune Function and Serum Levels of EGFR and Gastrin-Releasing Peptide Precursor (pro-GRP) in Patients with Non-Small-Cell Lung Cancer (NSCLC).
Disease markers | 2022-01-01 | PMID 36157204
Cao Wei, Ma Jun, Jiang Xuan and 1 more
Meta-Analysis of the Prognostic and Predictive Role of the CpG Island Methylator Phenotype in Colorectal Cancer.
Disease markers | 2022-01-01 | PMID 36157209
Wang Jing, Deng Zhujun, Lang Xiaoqiang and 8 more
Risk factors and diagnostic biomarkers for nonalcoholic fatty liver disease-associated hepatocellular carcinoma: Current evidence and future perspectives.
World journal of gastroenterology | 2022-07-21 | PMID 36158261
Ueno Masayuki, Takeda Haruhiko, Takai Atsushi and 1 more
Exosomal glypican-1 is elevated in pancreatic cancer precursors and can signal genetic predisposition in the absence of endoscopic ultrasound abnormalities.
World journal of gastroenterology | 2022-08-21 | PMID 36159010
Moutinho-Ribeiro Pedro, Batista Ines A, Quintas Sofia T and 18 more
Radiographic Phenotypes Affect the Risk of Inhaled Corticosteroid-Associated Pneumonia in Patients with COPD.
International journal of chronic obstructive pulmonary disease | 2022-01-01 | PMID 36159655
Lee Hyo Jin, Jin Kwang Nam, Lee Hyun Woo and 4 more
Immune depletion of the methylated phenotype of colon cancer is closely related to resistance to immune checkpoint inhibitors.
Frontiers in immunology | 2022-01-01 | PMID 36159794
Zhong Chengqian, Xie Tingjiang, Chen Long and 5 more
A specific immune signature for predicting the prognosis of glioma patients with IDH1-mutation and guiding immune checkpoint blockade therapy.
Frontiers in immunology | 2022-01-01 | PMID 36159801
Zeng Zhirui, Hu Chujiao, Ruan Wanyuan and 6 more
Integrated genomic, transcriptomic and metabolomic analysis reveals MDH2 mutation-induced metabolic disorder in recurrent focal segmental glomerulosclerosis.
Frontiers in immunology | 2022-01-01 | PMID 36159820
Shen Qixia, Teng Lisha, Wang Yucheng and 10 more
Are neurodegenerative diseases associated with an increased risk of inflammatory bowel disease? A two-sample Mendelian randomization study.
Frontiers in immunology | 2022-01-01 | PMID 36159838
Cui Guanghui, Li Shaojie, Ye Hui and 5 more
Characteristics of the immune microenvironment and their clinical significance in non-small cell lung cancer patients with ALK-rearranged mutation.
Frontiers in immunology | 2022-01-01 | PMID 36159860
Zhang Bo, Zeng Jingtong, Zhang Hao and 9 more
Causal effects of gut microbiota on diabetic retinopathy: A Mendelian randomization study.
Frontiers in immunology | 2022-01-01 | PMID 36159877
Liu Kangcheng, Zou Jing, Fan Huimin and 2 more
Molecular, Biochemical, and Clinical Characterization of Thirteen Patients with Glycogen Storage Disease 1a in Malaysia.
Genetics research | 2022-01-01 | PMID 36160031
Abdul Wahab Siti Aishah, Yakob Yusnita, Mohd Khalid Mohd Khairul Nizam and 3 more
Helicobacter pylori resistance to metronidazole and its association with virulence factors in a Moroccan population.
The Pan African medical journal | 2022-01-01 | PMID 36160282
Imane Essaidi, Ghizlane Bounder, Reda Jouimyi Mohamed and 6 more
Gastrointestinal tumors in transplantation: Two case reports and review of literature.
World journal of gastroenterology | 2022-09-14 | PMID 36160649
Stammler Romain, Anglicheau Dany, Landi Bruno and 4 more
ATM c.7570G>C is a high-risk allele for breast cancer.
International journal of cancer | 2023-02-01 | PMID 36161273
Kankuri-Tammilehto Minna, Tervasmäki Anna, Kraatari-Tiri Minna and 3 more
Prediction of Crohn's Disease Stricturing Phenotype Using a NOD2-derived Genomic Biomarker.
Inflammatory bowel diseases | 2023-04-03 | PMID 36161322
Ashton James J, Cheng Guo, Stafford Imogen S and 8 more
Sex-Specific Associations Between Susceptibility to Mycobacterium avium Complex Lung Disease and Programmed Cell Death 1 Gene Polymorphisms.
The Journal of infectious diseases | 2023-06-28 | PMID 36161323
Pan Sheng-Wei, Feng Jia-Yih, Wu Lawrence Shih-Hsin and 7 more
Epigenomic and somatic mutations of pituitary tumors with clinical and pathological correlations in 111 patients.
Clinical endocrinology | 2022-12-01 | PMID 36161330
Guaraldi Federica, Morandi Luca, Zoli Matteo and 8 more
Structural phenotypes of knee osteoarthritis: potential clinical and research relevance.
Skeletal radiology | 2023-11-01 | PMID 36161341
Roemer Frank W, Jarraya Mohamed, Collins Jamie E and 4 more
Integration of Universal Germline Genetic Testing for All New Breast Cancer Patients.
Annals of surgical oncology | 2023-02-01 | PMID 36161375
Culver Julie O, Freiberg Yael, Ricker Charité and 19 more
Loss-of-function mutations in SGCE found in Japanese patients with myoclonus-dystonia.
Clinical genetics | 2023-02-01 | PMID 36161439
Azuma Kenko, Horisawa Shiro, Mashimo Hideaki and 5 more
Review of genetic testing in kidney disease patients: Diagnostic yield of single nucleotide variants and copy number variations evaluated across and within kidney phenotype groups.
American journal of medical genetics. Part C, Seminars in medical genetics | 2022-09-01 | PMID 36161467
Claus Laura R, Snoek Rozemarijn, Knoers Nine V A M and 1 more
Adding gene transcripts into genomic prediction improves accuracy and reveals sampling time dependence.
G3 (Bethesda, Md.) | 2022-11-04 | PMID 36161485
Perez Bruno C, Bink Marco C A M, Svenson Karen L and 2 more
Metabolic phenotypes and incident type 2 diabetes: Population-based Panasonic cohort study 6.
Obesity (Silver Spring, Md.) | 2022-11-01 | PMID 36161537
Kobayashi Ayaka, Okada Hiroshi, Hamaguchi Masahide and 4 more
Returning individual genomic results to population-based cohort study participants with BRCA1/2 pathogenic variants.
Breast cancer (Tokyo, Japan) | 2023-01-01 | PMID 36161580
Ohneda Kinuko, Hamanaka Yohei, Kawame Hiroshi and 9 more
Determination of the relationship between major histocompatibility complex alleles and childhood onset obsessive-compulsive disorder.
Turkish journal of medical sciences | 2022-04-01 | PMID 36161604
Lüleyap Ümit, Karacaoğlan Gökhan, Tahiroğlu Ayşegül Yolga and 7 more
Validity and reliability of Fried frailty phenotype in Turkish population.
Turkish journal of medical sciences | 2022-04-01 | PMID 36161623
Varan Hacer Doğan, Deniz Olgun, Çöteli Süheyla and 3 more
TBX6 as a cause of a combined skeletal-kidney dysplasia syndrome.
American journal of medical genetics. Part A | 2022-12-01 | PMID 36161696
Li Guozhuang, Strong Alanna, Wang Haojun and 9 more
Identification of the novel HLA-C*12:02:47 allele in an individual from Maharashtra, India.
HLA | 2023-01-01 | PMID 36161710
Pinto Andrea S, Tambe Manisha, D'Silva Selma Z and 1 more
Familial aggregation of stillbirth: A pedigree analysis of a matched case-control study.
BJOG : an international journal of obstetrics and gynaecology | 2023-04-01 | PMID 36161750
Workalemahu Tsegaselassie, Page Jessica M, Meeks Huong and 12 more
Identification of nine mutant genes and establishment of three prediction models of organ tropism metastases of non-small cell lung cancer.
Cancer medicine | 2023-02-01 | PMID 36161776
Chen Shuchen, Huang Wanyi, Liu Zhenzhen and 13 more
Comparison of Nonsequencing Techniques for Identification of NPM1 Mutations and Associated Blast Morphology in Patients With Acute Myeloid Leukemia.
Archives of pathology & laboratory medicine | 2023-06-01 | PMID 36161791
Menegotto Pâmela Rossi, Farias Mariela Granero, Spagnol Fabiane and 4 more
Pathogenic genetic variants identified in Australian families with paediatric cataract.
BMJ open ophthalmology | 2022-08-01 | PMID 36161833
Jones Johanna L, McComish Bennet J, Staffieri Sandra E and 11 more
Exploring the mutational landscape of genes associated with inherited retinal disease using large genomic datasets: identifying loss of function intolerance and outlying propensities for missense changes.
BMJ open ophthalmology | 2022-08-01 | PMID 36161854
Tanner Alexander, Chan Hwei Wuen, Schiff Elena and 2 more
Genes: ADAMTS18, ALMS1, KCNV2, RP1L1, SAMD11, WFS1
Dissection of the long-range projections of specific neurons at the synaptic level in the whole mouse brain.
Proceedings of the National Academy of Sciences of the United States of America | 2022-10-04 | PMID 36161898
Tian Jiaojiao, Ren Miao, Zhao Peilin and 9 more
Using neuroimaging genomics to investigate the evolution of human brain structure.
Proceedings of the National Academy of Sciences of the United States of America | 2022-10-04 | PMID 36161899
Alagöz Gökberk, Molz Barbara, Eising Else and 4 more
Sperm-inherited H3K27me3 epialleles are transmitted transgenerationally in cis.
Proceedings of the National Academy of Sciences of the United States of America | 2022-10-04 | PMID 36161922
Kaneshiro Kiyomi Raye, Egelhofer Thea A, Rechtsteiner Andreas and 2 more
Redox status regulates autophagy in thymic stromal cells and promotes T cell tolerance.
Proceedings of the National Academy of Sciences of the United States of America | 2022-10-04 | PMID 36161925
Semwal Manpreet K, Hester Allison K, Xiao Yangming and 8 more
Modulation of receptor-like transmembrane kinase 1 nuclear localization by DA1 peptidases in Arabidopsis.
Proceedings of the National Academy of Sciences of the United States of America | 2022-10-04 | PMID 36161927
Gu Benguo, Dong Hui, Smith Caroline and 3 more
Genetic adaptation of skin pigmentation in highland Tibetans.
Proceedings of the National Academy of Sciences of the United States of America | 2022-10-04 | PMID 36161951
Yang Zhaohui, Bai Caijuan, Pu Youwei and 28 more
Changing patterns of genetic differentiation in the slender wild oat, Avena barbata.
Proceedings of the National Academy of Sciences of the United States of America | 2022-10-04 | PMID 36161958
Latta Robert G, Crosby Kate, Hamrick James L
Ruxolitinib in a Child With JAK2 Exon 12 Mutant Polycythemia Vera.
Journal of pediatric hematology/oncology | 2023-05-01 | PMID 36161965
Stoops Katie, Kuril Sandeepkumar
SGLT2 Inhibition, Choline Metabolites, and Cardiometabolic Diseases: A Mediation Mendelian Randomization Study.
Diabetes care | 2022-11-01 | PMID 36161993
Xu Min, Zheng Jie, Hou Tianzhichao and 10 more
Hermansky-Pudlak Syndrome: Spectrum in Oman.
Journal of pediatric hematology/oncology | 2023-04-01 | PMID 36162005
Nazir Hanan F, Al Sukaiti Nashat, Khater Doaa and 2 more
The role of cuticle in fruit shelf-life.
Current opinion in biotechnology | 2022-12-01 | PMID 36162185
Fernández-Muñoz Rafael, Heredia Antonio, Domínguez Eva
A novel ABA-insensitive mutant in Arabidopsis reveals molecular network of ABA-induced anthocyanin accumulation and abiotic stress tolerance.
Journal of plant physiology | 2022-11-01 | PMID 36162212
Shi Weijia, Wang Xiaojing, Liu Huan and 3 more
Molecular evaluation of gene mutation profiles and copy number variations in pediatric acute myeloid leukemia.
Leukemia research | 2022-11-01 | PMID 36162216
Meena Jagdish Prasad, Pathak Nivedita, Gupta Aditya Kumar and 4 more
Developmental behavioral genetics research on school achievement is missing vulnerable children, to our detriment.
New directions for child and adolescent development | 2022-07-01 | PMID 36162231
Holden LaTasha R, Haughbrook Rasheda, Hart Sara A
Advanced papillary renal cell carcinoma: Epidemiology, genomic drivers, current therapies, and ongoing trials.
Cancer treatment and research communications | 2022-01-01 | PMID 36162322
Sweeney Patrick L, Jang Albert, Halat Shams K and 2 more
Targeting GRP78 suppresses oncogenic KRAS protein expression and reduces viability of cancer cells bearing various KRAS mutations.
Neoplasia (New York, N.Y.) | 2022-11-01 | PMID 36162331
Ha Dat P, Huang Bo, Wang Han and 6 more
Genes: KRAS
Generation of two TMEM16A knockout iPSC clones each from a healthy human iPSC line, from a Cystic Fibrosis patient specific line with p.Phe508del mutation and from the gene corrected iPSC line.
Stem cell research | 2022-10-01 | PMID 36162332
Jaboreck Mark-Christian, Lühmann Jonathan Lukas, Mielenz Mia and 5 more
Generation of a human induced pluripotent stem cell line (LZUSHi002-A) from a MADD patient with ETFDH mutation.
Stem cell research | 2022-10-01 | PMID 36162333
Li Yan, Li Yuanxiao, Liu Hui and 4 more
Association between CYP2C19 and CYP2B6 phenotypes and the pharmacokinetics and safety of diazepam.
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie | 2022-11-01 | PMID 36162369
Zubiaur Pablo, Figueiredo-Tor Laura, Villapalos-García Gonzalo and 9 more
The N-terminal disease-associated R5L Tau mutation increases microtubule shrinkage rate due to disruption of microtubule-bound Tau patches.
The Journal of biological chemistry | 2022-11-01 | PMID 36162501
Cario Alisa, Wickramasinghe Sanjula P, Rhoades Elizabeth and 1 more
Mutations of Rad6 E2 ubiquitin-conjugating enzymes at alanine-126 in helix-3 affect ubiquitination activity and decrease enzyme stability.
The Journal of biological chemistry | 2022-11-01 | PMID 36162503
Shukla Prakash K, Sinha Dhiraj, Leng Andrew M and 7 more
Identification of a de novo LRP1 mutation in a Saudi family with Tetralogy of Fallot.
Gene | 2023-01-30 | PMID 36162527
Alrayes Nuha, Mallah Bayan A, Issa Noha M and 7 more
The CaV1.2 G406R mutation decreases synaptic inhibition and alters L-type Ca2+ channel-dependent LTP at hippocampal synapses in a mouse model of Timothy Syndrome.
Neuropharmacology | 2022-12-01 | PMID 36162529
Sanderson Jennifer L, Freund Ronald K, Castano Anna M and 2 more
Association Between Glycemic Traits and Primary Open-Angle Glaucoma: A Mendelian Randomization Study in the Japanese Population.
American journal of ophthalmology | 2023-01-01 | PMID 36162535
Hanyuda Akiko, Goto Atsushi, Nakatochi Masahiro and 25 more
Relation of CRP gene variants to altered risk of Helicobacter pylori - associated chronic gastritis: A case-control study in Tunisia.
Molecular and cellular probes | 2022-12-01 | PMID 36162594
Stayoussef Mouna, Zidi Sabrina, Kanabekova Perizat and 3 more
Reciprocal positive regulation between BRD4 and YAP in GNAQ-mutant uveal melanoma cells confers sensitivity to BET inhibitors.
Pharmacological research | 2022-10-01 | PMID 36162600
Zhang Gui-Ming, Huang Si-Si, Ye Lin-Xuan and 9 more
Causal influence of dietary habits on the risk of major depressive disorder: A diet-wide Mendelian randomization analysis.
Journal of affective disorders | 2022-12-15 | PMID 36162666
Chen Tzu-Ting, Chen Chia-Yen, Fang Chiu-Ping and 2 more
The «Amish» NM_000256.3:c.3330+2T>G splice variant in MYBPC3 associated with hypertrophic cardiomyopathy is an ancient Swiss mutation.
European journal of medical genetics | 2022-12-01 | PMID 36162733
Redin Claire, Pavlidou Despina Christina, Bhuiyan Zahurul and 11 more
Somatic variation in normal tissues: friend or foe of cancer early detection?
Annals of oncology : official journal of the European Society for Medical Oncology | 2022-12-01 | PMID 36162751
Acha-Sagredo A, Ganguli P, Ciccarelli F D
Disentangling the influences of parental genetics on offspring's cognition, education, and psychopathology via genetic and phenotypic pathways.
Journal of child psychology and psychiatry, and allied disciplines | 2023-03-01 | PMID 36162806
Axelrud Luiza K, Hoffmann Maurício S, Vosberg Daniel E and 13 more
Enhancing the BOADICEA cancer risk prediction model to incorporate new data on RAD51C, RAD51D, BARD1 updates to tumour pathology and cancer incidence.
Journal of medical genetics | 2022-12-01 | PMID 36162851
Lee Andrew, Mavaddat Nasim, Cunningham Alex and 19 more
Prospective validation of the BOADICEA multifactorial breast cancer risk prediction model in a large prospective cohort study.
Journal of medical genetics | 2022-12-01 | PMID 36162852
Yang Xin, Eriksson Mikael, Czene Kamila and 13 more
Nationwide retrospective observational study of idiopathic dendriform pulmonary ossification: clinical features with a progressive phenotype.
BMJ open respiratory research | 2022-09-01 | PMID 36162917
Nishioka Yasuhiko, Toyoda Yuko, Egashira Ryoko and 32 more
Inherited causes of combined vision and hearing loss: clinical features and molecular genetics.
The British journal of ophthalmology | 2023-10-01 | PMID 36162969
Guimaraes Thales Antonio Cabral de, Arram Elizabeth, Shakarchi Ahmed F and 2 more
Theoretical accuracy for indirect predictions based on SNP effects from single-step GBLUP.
Genetics, selection, evolution : GSE | 2022-09-27 | PMID 36162979
Garcia Andre, Aguilar Ignacio, Legarra Andres and 3 more
New pathogenic variants of ALMS1 gene in two Chinese families with Alström Syndrome.
BMC ophthalmology | 2022-09-26 | PMID 36162988
Cheng Wan-Yu, Ma Mei-Jiao, Yuan Shi-Qin and 3 more
Whole-genome sequencing reveals the genetic mechanisms of domestication in classical inbred mice.
Genome biology | 2022-09-26 | PMID 36163035
Liu Ming, Yu Caixia, Zhang Zhichao and 19 more
The neuropathologic findings in a case of progressive cavitating leukoencephalopathy due to NDUFV1 pathogenic variants.
Acta neuropathologica communications | 2022-09-26 | PMID 36163075
Becker Nicole, Sharma Aditi, Gosse Matthew and 2 more
Association analysis and expression level of ACE polymorphisms with egg-laying trait in Taihang chicken.
Poultry science | 2022-11-01 | PMID 36163094
Wang Peng, Li Kaiyang, Fan Yekai and 8 more
Association between the CTLA4 +49A/G (rs231775) and CT60 (rs3087243) gene variants with vitiligo: study on a Mexican population.
Anais brasileiros de dermatologia | 2000-01-01 | PMID 36163113
Salinas-Santander Mauricio Andrés, Suárez-Valencia Víctor de Jesús, Ángel-Martínez Mayela Del and 4 more
RAS oncogenic activity predicts response to chemotherapy and outcome in lung adenocarcinoma.
Nature communications | 2022-09-26 | PMID 36163168
East Philip, Kelly Gavin P, Biswas Dhruva and 7 more
Airway basal cells show a dedifferentiated KRT17highPhenotype and promote fibrosis in idiopathic pulmonary fibrosis.
Nature communications | 2022-09-26 | PMID 36163190
Jaeger Benedikt, Schupp Jonas Christian, Plappert Linda and 16 more
Association of cumulative excess weight and waist circumference exposure with transition from metabolically healthy obesity to metabolically unhealthy.
Nutrition, metabolism, and cardiovascular diseases : NMCD | 2022-11-01 | PMID 36163212
Jahromi Mitra Kazemi, Ebadinejad Amir, Barzin Maryam and 6 more
Genetic liability to sedentary behavior in relation to myocardial infarction and heart failure: A mendelian randomization study.
Nutrition, metabolism, and cardiovascular diseases : NMCD | 2022-11-01 | PMID 36163216
Yang Fangkun, Huangfu Ning, Chen Songzan and 5 more
Holocene climate changes explain the spatial pattern in genetic diversity in populations of Cyperus papyrus from Southeast Africa wetlands.
Heredity | 2022-11-01 | PMID 36163272
Maxombe Elias Luís, Vieira Lucas Donizetti, Sierens Tim and 2 more
Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroups.
Nature genetics | 2022-10-01 | PMID 36163277
Mattheisen Manuel, Grove Jakob, Als Thomas D and 31 more
Single-cell genome sequencing of human neurons identifies somatic point mutation and indel enrichment in regulatory elements.
Nature genetics | 2022-10-01 | PMID 36163278
Luquette Lovelace J, Miller Michael B, Zhou Zinan and 17 more
Graphdiyne oxide nanosheets display selective anti-leukemia efficacy against DNMT3A-mutant AML cells.
Nature communications | 2022-09-26 | PMID 36163326
Wang Qiwei, Liu Ying, Wang Hui and 22 more
Conformational change of RNA-helicase DHX30 by ALS/FTD-linked FUS induces mitochondrial dysfunction and cytosolic aggregates.
Scientific reports | 2022-09-26 | PMID 36163369
Hikiami Ryota, Morimura Toshifumi, Ayaki Takashi and 11 more
The comparison of cancer gene mutation frequencies in Chinese and U.S. patient populations.
Nature communications | 2022-09-26 | PMID 36163440
Ma Fayang, Laster Kyle, Dong Zigang
Retinal gene therapy in RPE-65 gene mediated inherited retinal dystrophy.
Eye (London, England) | 2023-06-01 | PMID 36163489
Jalil Assad, Ivanova Tsveta, Moussa George and 2 more
Variability of polyteny of giant chromosomes in Drosophila melanogaster salivary glands.
Genetica | 2023-02-01 | PMID 36163579
Strashnyuk Volodymyr Yu, Shakina Lyubov A, Skorobagatko Daria A