Effect of CYP2C19 polymorphisms on antidepressant prescription patterns and treatment emergent mania in bipolar disorder.
The pharmacogenomics journal | 2023-01-01 | PMID 36333412
Joas Erik, Jonsson Lina, Viktorin Alexander and 4 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 9036 of 10600
Founder lineages in the Iberian Roma mitogenomes recapitulate the Roma diaspora and show the effects of demographic bottlenecks.
Scientific reports | 2022-11-04 | PMID 36333436
Aizpurua-Iraola Julen, Giménez Aaron, Carballo-Mesa Annabel and 2 more
Live birth in a 47-million-year-old snake.
Die Naturwissenschaften | 2022-11-05 | PMID 36333469
Chuliver Mariana, Scanferla Agustín, Smith Krister T
Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis.
Nature genetics | 2022-11-01 | PMID 36333501
Ishigaki Kazuyoshi, Sakaue Saori, Terao Chikashi and 87 more
Whole-genome sequencing of chronic lymphocytic leukemia identifies subgroups with distinct biological and clinical features.
Nature genetics | 2022-11-01 | PMID 36333502
Robbe Pauline, Ridout Kate E, Vavoulis Dimitrios V and 38 more
Real-World Study of Regional Differences in Patient Demographics, Clinical Characteristics, and BRCA1/2 Mutation Testing in Patients with Human Epidermal Growth Factor Receptor 2-Negative Advanced Breast Cancer in the United States, Europe, and Israel.
Advances in therapy | 2023-01-01 | PMID 36333567
Mahtani Reshma, Niyazov Alexander, Lewis Katie and 4 more
Identification and interrogation of the gene regulatory network of CEBPA-double mutant acute myeloid leukemia.
Leukemia | 2023-01-01 | PMID 36333583
Adamo Assunta, Chin Paulynn, Keane Peter and 9 more
An infant with congenital heart defects and proteinuria: a case report.
BMC pediatrics | 2022-11-04 | PMID 36333735
Liu Dandan, Wang Yafeng
Longitudinal phenotypes in patients with acute respiratory distress syndrome: a multi-database study.
Critical care (London, England) | 2022-11-04 | PMID 36333766
Chen Hui, Yu Qian, Xie Jianfeng and 7 more
Macrophage polarization toward M1 phenotype through NF-κB signaling in patients with Behçet's disease.
Arthritis research & therapy | 2022-11-04 | PMID 36333776
Wu Xiuhua, Wang Zhimian, Shi Jing and 6 more
Stem cell phenotype predicts therapeutic response in glioblastomas with MGMT promoter methylation.
Acta neuropathologica communications | 2022-11-04 | PMID 36333778
Lakis Nelli S, Brodsky Alexander S, Karashchuk Galina and 7 more
Lack of causal association between heart failure and osteoporosis: a Mendelian randomization study.
BMC medical genomics | 2022-11-04 | PMID 36333784
Chen Heng, Ye Runze, Guo Xiaogang
Genomic landscape, immune characteristics and prognostic mutation signature of cervical cancer in China.
BMC medical genomics | 2022-11-04 | PMID 36333792
Liu Jing, Li Zirong, Lu Ting and 7 more
Compound Heterozygote Mutation in the SMPD1 Gene Leading to Nieman-Pick Disease Type A.
The American journal of case reports | 2022-11-05 | PMID 36333862
Kavčič Alja, Homan Matjaž, Živanović Milanka and 7 more
Investigation of mutations in Fanconi anemia genes and malignancy predisposition in Brazilian patients.
International journal of laboratory hematology | 2023-02-01 | PMID 36333938
Pillonetto Daniela Vandresen, Piovezan Bruno Zagonel, Nichele Samantha and 4 more
SCAF4-related syndromic intellectual disability.
American journal of medical genetics. Part A | 2023-02-01 | PMID 36333968
Carvalho Laura Machado Lara, Pinto Carla Franchi, de Oliveira Scliar Marília and 3 more
A severe clinicopathologic phenotype of RAF1 Ser257Leu neomutation in a preterm infant without cardiac anomaly.
American journal of medical genetics. Part A | 2023-02-01 | PMID 36333975
Darouich Sihem, Chakroun Ahmed Sahbi, Bellamine Houda and 1 more
Assessment of an automated approach for variant interpretation in screening for monogenic disorders: A single-center study.
Molecular genetics & genomic medicine | 2022-12-01 | PMID 36333997
Gall Bryan J, Smart Trevor B, Munch Robin and 8 more
Low-grade duodenal eosinophilia is associated with cagA in Helicobacter pylori-related dyspepsia.
Journal of gastroenterology and hepatology | 2023-02-01 | PMID 36334009
Barreyro Fernando Javier, Sanchez Nicolas, Caronia Maria Virginia and 4 more
Identification of the novel class II allele, HLA-DPA1*01:127.
HLA | 2023-02-01 | PMID 36334043
Jeong In Hwa, Eom So Hyun, Lim Sori and 1 more
A 'wiring diagram' for sink strength traits impacting wheat yield potential.
Journal of experimental botany | 2023-01-01 | PMID 36334052
Slafer Gustavo A, Foulkes M John, Reynolds Matthew P and 6 more
Recognizing early MRI signs (or their absence) is crucial in diagnosing metachromatic leukodystrophy.
Annals of clinical and translational neurology | 2022-12-01 | PMID 36334091
Schoenmakers Daphne H, Beerepoot Shanice, Krägeloh-Mann Ingeborg and 5 more
The First Compound Heterozygous Mutations of DMP1 Causing Rare Autosomal Recessive Hypophosphatemic Rickets Type 1.
The Journal of clinical endocrinology and metabolism | 2023-03-10 | PMID 36334264
Ni Xiaolin, Gong Yiyi, Jiang Yan and 9 more
The prediction accuracies of linear-type traits in Czech Holstein cattle when using ssGBLUP or wssGBLUP.
Journal of animal science | 2022-12-01 | PMID 36334266
Brzáková Michaela, Bauer Jiří, Steyn Yvette and 2 more
Leptomeningeal metastases in glioma revisited: incidence and molecular predictors based on postcontrast fluid-attenuated inversion recovery imaging.
Journal of neurosurgery | 2023-07-01 | PMID 36334295
Park Yae Won, Han Kyunghwa, Park Ji Eun and 7 more
Sierra SARS-CoV-2 sequence and antiviral resistance analysis program.
Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology | 2022-12-01 | PMID 36334368
Tzou Philip L, Tao Kaiming, Sahoo Malaya K and 3 more
Genome-wide association analysis of the primary feather growth traits of duck: identification of potential Loci for growth regulation.
Poultry science | 2023-01-01 | PMID 36334470
Ma Shengchao, Li Pengcheng, Liu Hehe and 10 more
Causal associations between obstructive sleep apnea and COVID-19: A bidirectional Mendelian randomization study.
Sleep medicine | 2023-01-01 | PMID 36334498
Gao Xiang, Wei Tao, Wang Huijun and 4 more
A theoretical study on binding and stabilization of galactose and novel galactose analogues to the human α-galactosidase A variant causing Fabry disease.
Biophysical chemistry | 2023-01-01 | PMID 36334502
Klaewkla Methus, Prousoontorn Jittithorn, Charoenwongpaiboon Thanapon
Generation of human induced pluripotent stem cells (CHULAi001-A) from peripheral blood mononuclear cells of a glucose-6-phosphate dehydrogenase (G6PD) deficient subject carrying the Viangchan mutation.
Stem cell research | 2022-12-01 | PMID 36334578
Tongbaen Malinee, Matsumura Yasuko, Okita Keisuke and 1 more
Mendelian randomization and pathway analysis demonstrate shared genetic associations between lupus and coronary artery disease.
Cell reports. Medicine | 2022-11-15 | PMID 36334592
Kain Jessica, Owen Katherine A, Marion Miranda C and 3 more
A de novo mutation (p.S1419F) of Retinoic acid induced 1 is responsible for a patient with Smith-Magenis syndrome exhibiting schizophrenia.
Gene | 2023-01-30 | PMID 36334618
Yu Rong, Liu Lv, Chen Chan and 3 more
Mutations in the α4-α5 allosteric lobe of RAS do not significantly impair RAS signaling or self-association.
The Journal of biological chemistry | 2022-12-01 | PMID 36334633
Whaby Michael, Wallon Lauren, Mazzei Megan and 4 more
Histological types of lung cancer attributable to fine particulate, smoking, and genetic susceptibility.
The Science of the total environment | 2023-02-01 | PMID 36334679
Wang Xiaojie, Wang Tingting, Hua Junjie and 8 more
Loss-of-function mutations in melanocortin-1 receptor modulate immune response in teleost fishes.
Fish & shellfish immunology | 2022-12-01 | PMID 36334699
Fierro-Castro Camino, Rotllant Josep, Cerdá-Reverter Jose Miguel and 1 more
Unmasking the Conformational Stability and Inhibitor Binding to SARS-CoV-2 Main Protease Active Site Mutants and Miniprecursor.
Journal of molecular biology | 2022-12-30 | PMID 36334779
Kovalevsky Andrey, Coates Leighton, Kneller Daniel W and 4 more
Incorporating second-tier genetic screening for multiple acyl-CoA dehydrogenase deficiency.
Clinica chimica acta; international journal of clinical chemistry | 2022-12-01 | PMID 36334790
Lin Yiming, Zheng Wenwei, Chen Yanru and 4 more
Myeloid- and hepatocyte-specific deletion of group VIA calcium-independent phospholipase A2 leads to dichotomous opposing phenotypes during MCD diet-induced NASH.
Biochimica et biophysica acta. Molecular basis of disease | 2023-01-01 | PMID 36334837
Jansakun Chutima, Chunglok Warangkana, Altamura Sandro and 5 more
Bisphenol A exposure modulates reproductive and endocrine system, mitochondrial function and cellular senescence in female adult rats: A hallmarks of polycystic ovarian syndrome phenotype.
Environmental toxicology and pharmacology | 2022-11-01 | PMID 36334871
Prabhu Navya B, Adiga Divya, Kabekkodu Shama Prasada and 3 more
Lactase persistence phenotype and genotype in Iranian Mazani-Shahmirzadi and Afghan Hazara ethnicities.
European journal of medical genetics | 2022-12-01 | PMID 36334882
Rajabloo Servin, Marefat Ezatullah, Hassan-Zadeh Vahideh
Phenotype expansion and neurological manifestations of neurobehavioural disease caused by a variant in RFX7.
European journal of medical genetics | 2023-01-01 | PMID 36334883
Ledger Marissa L, Kaare Milja, Mailo Janette A and 1 more
Hydranencephaly in CENPJ-related Seckel syndrome.
European journal of medical genetics | 2022-12-01 | PMID 36334884
Cuccurullo Claudia, Miele Giuseppina, Piccolo Gianluca and 10 more
Sex-specific genetic association of brain and muscle Arnt-like protein-1 (BMAL1) and obesity in Chinese youth.
Obesity research & clinical practice | 2000-01-01 | PMID 36335026
Fang Zhengmei, Zhu Lijun, Zhang Tao and 3 more
HLA-A, -B, -C, -DPB1, -DQB1 and -DRB1 allele frequencies of North Tanzanian Maasai.
Human immunology | 2023-02-01 | PMID 36335052
Barton Amber, Ramadhani Athumani, Mafuru Elias and 11 more
Sequence based HLA-DRB1, -DQB1 and -DPB1 allele and haplotype frequencies in The Gambia.
Human immunology | 2023-02-01 | PMID 36335053
Barton Amber, Pickering Harry, Payne Thomas and 7 more
Ancestry-defined molecular taxonomy of prostate cancer.
Trends in cancer | 2022-12-01 | PMID 36335083
Elhussin Isra, Yates Clayton
Analysis of clinically relevant variants from ancestrally diverse Asian genomes.
Nature communications | 2022-11-05 | PMID 36335097
Chan Sock Hoai, Bylstra Yasmin, Teo Jing Xian and 29 more
Parent-of-Origin inference for biobanks.
Nature communications | 2022-11-05 | PMID 36335127
Hofmeister Robin J, Rubinacci Simone, Ribeiro Diogo M and 3 more
Molecular profile and its clinical impact of IDH1 mutated versus IDH1 wild type intrahepatic cholangiocarcinoma.
Scientific reports | 2022-11-05 | PMID 36335135
Rimini Margherita, Fabregat-Franco Carles, Burgio Valentina and 22 more
Correlation of T1- to T2-weighted signal intensity ratio with T1- and T2-relaxation time and IDH mutation status in glioma.
Scientific reports | 2022-11-05 | PMID 36335158
Sanada Takahiro, Yamamoto Shota, Sakai Mio and 11 more
Influences of maternal factors on the estimate of genetic parameters for goat feed efficiency traits.
Tropical animal health and production | 2022-11-05 | PMID 36335175
Singh Manoj Kumar, Dige Mahesh Shivanand, Pourouchottamane R and 2 more
Genetic insights into smoking behaviours in 10,558 men of African ancestry from continental Africa and the UK.
Scientific reports | 2022-11-05 | PMID 36335192
Piga Noemi-Nicole, Boua Palwende Romuald, Soremekun Chisom and 8 more
Effects of cancer-associated point mutations on the structure, function, and stability of isocitrate dehydrogenase 2.
Scientific reports | 2022-11-05 | PMID 36335201
Chen Xiang, Yang Peipei, Qiao Yue and 7 more
Association between the interleukin-1B polymorphism at rs16944 T>C and diabetic retinopathy.
International journal of immunogenetics | 2023-02-01 | PMID 36335222
Lin Nengbo, Lu Hua, Cheng Xiaoling and 7 more
Analysis of the twenty-six largest outbreaks of tuberculosis in Aragon using whole-genome sequencing for surveillance purposes.
Scientific reports | 2022-11-05 | PMID 36335223
Comín Jessica, Cebollada Alberto, Ibarz Daniel and 5 more
The effect of mutations on binding interactions between the SARS-CoV-2 receptor binding domain and neutralizing antibodies B38 and CB6.
Scientific reports | 2022-11-05 | PMID 36335244
Barnes Jonathan E, Lund-Andersen Peik K, Patel Jagdish Suresh and 1 more
BMPMDA: Prediction of MiRNA-Disease Associations Using a Space Projection Model Based on Block Matrix.
Interdisciplinary sciences, computational life sciences | 2023-03-01 | PMID 36335274
Shen Yi, Liu Jin-Xing, Yin Meng-Meng and 2 more
Phenotypic differences among and within extant populations of Chrysanthemum arcticum L. and C. a. subsp. arcticum.
BMC plant biology | 2022-11-05 | PMID 36335304
Liu Yunjia, Anderson Neil O
The rs35874116 single nucleotide polymorphism increases sweet intake and the risk of severe early childhood caries: a case-control study.
BMC oral health | 2022-11-05 | PMID 36335309
Liang Yan, Yao Junyu, Qiu Rongmin and 4 more
ALDH2 gene polymorphism is associated with fitness in the elderly Japanese population.
Journal of physiological anthropology | 2022-11-05 | PMID 36335382
De Almeida Kathleen Yasmin, Saito Mika, Homma Hiroki and 7 more
Determination of critical concentration for drug susceptibility testing of Mycobacterium tuberculosis against para-aminosalicylic acid with clinical isolates with thyA, folC and dfrA mutations.
Annals of clinical microbiology and antimicrobials | 2022-11-05 | PMID 36335391
Wang Wei, Li Shanshan, Ge Qiping and 7 more
Deciphering the impact of genetic variation on human polyadenylation using APARENT2.
Genome biology | 2022-11-05 | PMID 36335397
Linder Johannes, Koplik Samantha E, Kundaje Anshul and 1 more
A genome-wide association study of survival in patients with sepsis.
Critical care (London, England) | 2022-11-05 | PMID 36335405
Hernandez-Beeftink Tamara, Guillen-Guio Beatriz, Lorenzo-Salazar Jose M and 30 more
Whole-exome sequencing identified a homozygous novel RAG1 mutation in a child with omenn syndrome.
Allergologia et immunopathologia | 2022-01-01 | PMID 36335443
Wang Wendi, Wang Jian, Wang Jingjing and 8 more
Targeted Locus Amplification and Haplotyping.
Methods in molecular biology (Clifton, N.J.) | 2023-01-01 | PMID 36335490
Lefferts Juliet W, Boersma Vera, Hagemeijer Marne C and 3 more
Read-Based Phasing and Analysis of Phased Variants with WhatsHap.
Methods in molecular biology (Clifton, N.J.) | 2023-01-01 | PMID 36335496
Martin Marcel, Ebert Peter, Marschall Tobias
HapCUT2: A Method for Phasing Genomes Using Experimental Sequence Data.
Methods in molecular biology (Clifton, N.J.) | 2023-01-01 | PMID 36335497
Bansal Vikas
Determining Complete Chromosomal Haplotypes by mLinker.
Methods in molecular biology (Clifton, N.J.) | 2023-01-01 | PMID 36335498
Sinha Sumit, Zhang Cheng-Zhong
Chromosome-Length Haplotypes with StrandPhaseR and Strand-seq.
Methods in molecular biology (Clifton, N.J.) | 2023-01-01 | PMID 36335500
Hanlon Vincent C T, Porubsky David, Lansdorp Peter M
Phasing DNA Methylation.
Methods in molecular biology (Clifton, N.J.) | 2023-01-01 | PMID 36335502
Akbari Vahid, Jones Steven J M
Analysis of 1276 Haplotype-Resolved Genomes Allows Characterization of Cis- and Trans-Abundant Genes.
Methods in molecular biology (Clifton, N.J.) | 2023-01-01 | PMID 36335503
Hoehe Margret R, Herwig Ralf
Phased Genome Assemblies.
Methods in molecular biology (Clifton, N.J.) | 2023-01-01 | PMID 36335504
Duitama Jorge
Chinese Pedigree of Chronic Mucocutaneous Candidiasis Due to STAT1 Gain-of-Function Mutation: A Case Study and Literature Review.
Mycopathologia | 2023-04-01 | PMID 36335528
Wang Xu, Zhao Weiwei, Chen Feng and 2 more
Classification of Parkinson's disease motor phenotype: a machine learning approach.
Journal of neural transmission (Vienna, Austria : 1996) | 2022-12-01 | PMID 36335541
Shirahige Lívia, Leimig Brenda, Baltar Adriana and 9 more
Canine gastrointestinal stromal tumours treated with surgery and imatinib mesylate: three cases (2018-2020).
The Journal of small animal practice | 2023-03-01 | PMID 36335646
Treggiari E, Giantin M, Ferro S and 1 more
Design, synthesis, AML activity and molecular modeling of novel IDH2 inhibitors.
Bioorganic chemistry | 2023-01-01 | PMID 36335650
Jin Ruyi, Tang Tian, Zhou Sha and 4 more
Novel mutations in TUBB8 and ZP3 cause human oocyte maturation arrest and female infertility.
European journal of obstetrics, gynecology, and reproductive biology | 2022-12-01 | PMID 36335766
Li Wenbo, Li Qian, Xu Xiqiao and 3 more
Real-world data with afatinib in Spanish patients with treatment-naïve non-small-cell lung cancer harboring exon 19 deletions in epidermal growth factor receptor (Del19 EGFR): Clinical experience of the Galician Lung Cancer Group.
Cancer treatment and research communications | 2022-01-01 | PMID 36335799
Agraso Sara, Lázaro Martin, Firvida Xose Luis and 11 more
Generation of one human induced pluripotent stem cell line (XACHi004-A) with heterozygous mutation of RYR2 gene from an atrial fibrillation patient.
Stem cell research | 2022-12-01 | PMID 36335801
Zhou Yafei, Jiang Congshan, Wang Jie and 3 more
Heteroplasmic Mutant Load Differences in Mitochondrial DNA-Associated Leigh Syndrome.
Pediatric neurology | 2023-01-01 | PMID 36335839
Na Ji-Hoon, Lee Young-Mock
Relationship between genetic polymorphisms of cytokines and self-reported sleep complaints and habitual caffeine consumption.
Sleep medicine | 2023-01-01 | PMID 36335893
Drogou Catherine, Erblang Mégane, Metlaine Arnaud and 10 more
Computational modeling of the effect of five mutations on the structure of the ACE2 receptor and their correlation with infectivity and virulence of some emerged variants of SARS-CoV-2 suggests mechanisms of binding affinity dysregulation.
Chemico-biological interactions | 2022-12-01 | PMID 36336003
Rodriguez J A, Gonzalez J, Arboleda-Bustos C E and 3 more
Molecular etiology of defective nuclear and mitochondrial ribosome biogenesis: Clinical phenotypes and therapy.
Biochimie | 2023-04-01 | PMID 36336106
Jerome Maria Sona, Nanjappa Dechamma Pandyanda, Chakraborty Anirban and 1 more
ESR1 activating mutations: From structure to clinical application.
Biochimica et biophysica acta. Reviews on cancer | 2023-01-01 | PMID 36336145
Grinshpun Albert, Chen Vincent, Sandusky Zachary M and 2 more
Genes: ESR1
Evaluating a species phylogeny using ddRAD SNPs: Cyto-nuclear discordance and introgression in the salmonid genus Thymallus (Salmonidae).
Molecular phylogenetics and evolution | 2023-01-01 | PMID 36336233
Secci-Petretto Giulia, Englmaier Gernot K, Weiss Steven J and 7 more
Can the genetic variability of Blastocystis sp. be associated with the climatic region of its human carriers?
Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases | 2022-12-01 | PMID 36336275
Ake-Canche B, Rodriguez-Bataz E, Esquivel-Piña J Y and 9 more
A novel splicing mutation of ANK1 is associated with phenotypic heterogeneity of hereditary spherocytosis in a Chinese family.
Biochimica et biophysica acta. Molecular basis of disease | 2023-01-01 | PMID 36336297
Xu Linlin, Wei Xiaofeng, Liang Guanxia and 4 more
Clinical and genetic characteristics of the patients with hypertension and hypokalemia carrying a novel SCNN1A mutation.
Scandinavian journal of clinical and laboratory investigation | 2000-01-01 | PMID 36336351
Chen Mengzi, Lv Xi, Li Jiwu and 2 more
Detection and analysis of DNA mixtures with the MiSeq FGx®.
Science & justice : journal of the Forensic Science Society | 2022-09-01 | PMID 36336448
Gutierrez Ryan, Roman Madeline, Houston Rachel and 1 more
Treatment of hereditary amyotrophic lateral sclerosis.
Revue neurologique | 2000-01-01 | PMID 36336493
Corcia P, Blasco H, Beltran S and 2 more
Classic Timothy Syndrome Associated With Bilateral Border Digit Syndactyly: A Case Series.
The Journal of hand surgery | 2024-08-01 | PMID 36336572
Zheng Eugene E, Avila Francisco R, Ackerman Michael J and 1 more
Adenoviruses in medicine: innocuous pathogen, predator, or partner.
Trends in molecular medicine | 2023-01-01 | PMID 36336610
MacNeil Katelyn M, Dodge Mackenzie J, Evans Andris M and 3 more
Functional connectivity response to acute pain assessed by fNIRS is associated with BDNF genotype in fibromyalgia: an exploratory study.
Scientific reports | 2022-11-06 | PMID 36336706
de Oliveira Franco Álvaro, de Oliveira Venturini Guilherme, da Silveira Alves Camila Fernanda and 8 more
Genetic prediction of male pattern baldness based on large independent datasets.
European journal of human genetics : EJHG | 2023-03-01 | PMID 36336714
Chen Yan, Hysi Pirro, Maj Carlo and 4 more
Molecular Pathogenesis of Myeloproliferative Neoplasms.
Current hematologic malignancy reports | 2022-12-01 | PMID 36336766
Rolles Benjamin, Mullally Ann
Novel STAT1 Variants in Japanese Patients with Isolated Mendelian Susceptibility to Mycobacterial Diseases.
Journal of clinical immunology | 2023-02-01 | PMID 36336768
Ono Rintaro, Tsumura Miyuki, Shima Saho and 16 more
Migratory behaviour is positively associated with genetic diversity in butterflies.
Molecular ecology | 2023-02-01 | PMID 36336800
García-Berro Aurora, Talla Venkat, Vila Roger and 6 more
Conspicuous coloration of toxin-resistant predators implicates additional trophic interactions in a predator-prey arms race.
Molecular ecology | 2023-08-01 | PMID 36336815
Hague Michael T J, Miller Lauren E, Stokes Amber N and 3 more
The Potential of Low Phytic Acid1-1 Mutant in Maize (Zea mays L.): A Sustainable Solution to Non-Renewable Phosphorus.
Frontiers in bioscience (Landmark edition) | 2022-10-14 | PMID 36336866
Colombo Federico, Sangiorgio Stefano, Abruzzese Alessandro and 5 more
Positive predictive value of a single nucleotide polymorphism (SNP)-based NIPT for aneuploidy in twins: Experience from clinical practice.
Prenatal diagnosis | 2022-12-01 | PMID 36336878
Kantor Valerie, Mo Lihong, DiNonno Wendy and 7 more