Works matching IS 14739542 AND DT 2024 AND VI 18

Results: 135

Shared genetic effect of kidney function on bipolar and major depressive disorders: a large-scale genome-wide cross-trait analysis.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00627-3

By:

Yu, Simin;
Lin, Yifei;
Yang, Yong;
Jin, Xi;
Liao, Banghua;
Lu, Donghao;
Huang, Jin

Publication type:

Article

Genetic analysis of 106 sporadic cases with hearing loss in the UAE population.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00630-8

By:

Tlili, Abdelaziz;
Mahfood, Mona;
Al Mutery, Abdullah;
Chouchen, Jihen

Publication type:

Article

Deep learning-based pathway-centric approach to characterize recurrent hepatocellular carcinoma after liver transplantation.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00624-6

By:

To, Jeffrey;
Ghosh, Soumita;
Zhao, Xun;
Pasini, Elisa;
Fischer, Sandra;
Sapisochin, Gonzalo;
Ghanekar, Anand;
Jaeckel, Elmar;
Bhat, Mamatha

Publication type:

Article

Sperm epigenetics and male infertility: unraveling the molecular puzzle.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00626-4

By:

Hosseini, Maryam;
Khalafiyan, Anis;
Zare, Mohammadreza;
Karimzadeh, Haniye;
Bahrami, Basireh;
Hammami, Behnaz;
Kazemi, Mohammad

Publication type:

Article

Mendelian randomization evidence based on European ancestry for the causal effects of leukocyte telomere length on prostate cancer.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00622-8

By:

Wu, Xinrui;
Hu, Cong;
Wu, Tianyang;
Du, Xinxing;
Peng, Zehong;
Xue, Wei;
Chen, Yonghui;
Dong, Liang

Publication type:

Article

Pan-cancer analysis of CDKN2A alterations identifies a subset of gastric cancer with a cold tumor immune microenvironment.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00615-7

By:

Deng, Chao;
Li, Zi-xi;
Xie, Chen-jun;
Zhang, Qing-lin;
Hu, Ben-shun;
Wang, Mei-dan;
Mei, Jie;
Yang, Chen;
Zhong, Zhangfeng;
Wang, Ke-wei

Publication type:

Article

Assessment of nucleic acid extraction protocols for antibiotic resistance genes (ARGs) quantification in aircraft wastewater.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00617-5

By:

Smith, Wendy J. M.;
Liu, Yawen;
Simpson, Stuart L.;
Bivins, Aaron;
Ahmed, Warish

Publication type:

Article

Evolutionary and functional analyses of LRP5 in archaic and extant modern humans.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00616-6

By:

Roca-Ayats, Neus;
Maceda, Iago;
Bruque, Carlos David;
Martínez-Gil, Núria;
Garcia-Giralt, Natàlia;
Cozar, Mónica;
Mellibovsky, Leonardo;
Van Hul, Wim;
Lao, Oscar;
Grinberg, Daniel;
Balcells, Susanna

Publication type:

Article

Critical insights on "Association of the C allele of rs479200 in the EGLN1 gene with COVID‑19 severity in Indian population: a novel finding".

Published in:

2024

By:

Deora, Nimita;
Agrohi, Priya;
Mallick, Prashant K;
Sinha, Abhinav

Publication type:

Letter

Polygenic risk score predicting susceptibility and outcome of benign prostatic hyperplasia in the Han Chinese.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00619-3

By:

Hung, Sheng-Chun;
Chang, Li-Wen;
Hsiao, Tzu-Hung;
Lin, Guan-Cheng;
Wang, Shian-Shiang;
Li, Jian-Ri;
Chen, I-Chieh

Publication type:

Article

A genome-wide association study identifies candidate genes for sleep disturbances in depressed individuals.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00609-5

By:

Yang, Xuena;
Cheng, Bolun;
Cheng, Shiqiang;
Liu, Li;
Pan, Chuyu;
Meng, Peilin;
Li, Chun'e;
Chen, Yujing;
Zhang, Jingxi;
Zhang, Huijie;
Zhang, Zhen;
Wen, Yan;
Jia, Yumeng;
Liu, Huan;
Zhang, Feng

Publication type:

Article

An RNA-seq study in Friedreich ataxia patients identified hsa-miR-148a-3p as a putative prognostic biomarker of the disease.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00602-y

By:

Vancheri, Chiara;
Quatrana, Andrea;
Morini, Elena;
Mariotti, Caterina;
Mongelli, Alessia;
Fichera, Mario;
Rufini, Alessandra;
Condò, Ivano;
Testi, Roberto;
Novelli, Giuseppe;
Malisan, Florence;
Amati, Francesca

Publication type:

Article

Simultaneous detection of influenza A, B and respiratory syncytial virus in wastewater samples by one-step multiplex RT-ddPCR assay.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00614-8

By:

Zafeiriadou, Anastasia;
Kaltsis, Lazaros;
Thomaidis, Nikolaos S.;
Markou, Athina

Publication type:

Article

Meta-analysis of genomic variants in power and endurance sports to decode the impact of genomics on athletic performance and success.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00621-9

By:

Psatha, Aikaterini;
Al-Mahayri, Zeina N.;
Mitropoulou, Christina;
Patrinos, George P.

Publication type:

Article

Development, validation and application of single molecule molecular inversion probe based novel integrated genetic screening method for 29 common lysosomal storage disorders in India.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00613-9

By:

Sheth, Harsh;
Nair, Aadhira;
Bhavsar, Riddhi;
Kamate, Mahesh;
Gowda, Vykuntaraju K.;
Bavdekar, Ashish;
Kadam, Sandeep;
Nampoothiri, Sheela;
Panigrahi, Inusha;
Kaur, Anupriya;
Shah, Siddharth;
Mehta, Sanjeev;
Jagadeesan, Sujatha;
Suresh, Indrani;
Kapoor, Seema;
Bajaj, Shruti;
Devi, Radha Rama;
Prajapati, Ashka;
Godbole, Koumudi;
Patel, Harsh

Publication type:

Article

Australian public perspectives on genomic newborn screening: which conditions should be included?

Published in:

Human Genomics, 2024, v. 18, p. 1, doi. 10.1186/s40246-024-00611-x

By:

Lynch, Fiona;
Best, Stephanie;
Gaff, Clara;
Downie, Lilian;
Archibald, Alison D.;
Gyngell, Christopher;
Goranitis, Ilias;
Peters, Riccarda;
Savulescu, Julian;
Lunke, Sebastian;
Stark, Zornitza;
Vears, Danya F.

Publication type:

Article

Epidemiologic association and shared genetic architecture between cataract and hearing difficulties among middle-aged and older adults.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00601-z

By:

Zhang, Xiayin;
Wang, Shan;
Liu, Shunming;
Du, Zijing;
Wu, Guanrong;
Liang, Yingying;
Huang, Yu;
Shang, Xianwen;
Hu, Yijun;
Zhu, Zhuoting;
Sun, Wei;
Zhang, Xueli;
Yu, Honghua

Publication type:

Article

GEN1 as a risk factor for human congenital anomalies of the kidney and urinary tract.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00606-8

By:

Xuanjin Du;
Chunyan Wang;
Jialu Liu;
Minghui Yu;
Haixin Ju;
Shanshan Xue;
Yaxin Li;
Jiaojiao Liu;
Rufeng Dai;
Jing Chen;
Yihui Zhai;
Jia Rao;
Xiang Wang;
Yubo Sun;
Lei Sun;
Xiaohui Wu;
Hong Xu;
Qian Shen

Publication type:

Article

Mendelian randomization and colocalization analysis reveal novel drug targets for myasthenia gravis.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00607-7

By:

Ouyang, Yuzhen;
Chen, Yu;
Chen, Kangzhi;
Tang, Zhenwei;
Shi, Guanzhong;
Qu, Chunrun;
Zhang, Kaiyue;
Yang, Huan

Publication type:

Article

Prioritization of therapeutic targets for cancers using integrative multi-omics analysis.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00571-2

By:

Jin, Xin;
Mei, Yunyun;
Yang, Puyu;
Huang, Runze;
Zhang, Haifeng;
Wu, Yibin;
Wang, Miao;
He, Xigan;
Jiang, Ziting;
Zhu, Weiping;
Wang, Lu

Publication type:

Article

Meta-analysis of the global distribution of clinically relevant CYP2C8 alleles and their inferred functional consequences.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00610-y

By:

Camara, Mahamadou D.;
Zhou, Yitian;
De Sousa, Taís Nóbrega;
Gil, José P.;
Djimde, Abdoulaye A.;
Lauschke, Volker M.

Publication type:

Article

Critical assessment of variant prioritization methods for rare disease diagnosis within the rare genomes project.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00604-w

By:

Stenton, Sarah L.;
O'Leary, Melanie C.;
Lemire, Gabrielle;
VanNoy, Grace E.;
DiTroia, Stephanie;
Ganesh, Vijay S.;
Groopman, Emily;
O'Heir, Emily;
Mangilog, Brian;
Osei-Owusu, Ikeoluwa;
Pais, Lynn S.;
Serrano, Jillian;
Singer-Berk, Moriel;
Weisburd, Ben;
Wilson, Michael W.;
Austin-Tse, Christina;
Abdelhakim, Marwa;
Althagafi, Azza;
Babbi, Giulia;
Bellazzi, Riccardo

Publication type:

Article

The causal associations of circulating lipids with Barrett's Esophagus and Esophageal Cancer: a bi-directional, two sample mendelian randomization analysis.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00608-6

By:

Li, Baofeng;
Li, Meng;
Qi, Xiao;
Tong, Ti;
zhang, Guangxin

Publication type:

Article

FiTMuSiC: leveraging structural and (co)evolutionary data for protein fitness prediction.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00605-9

By:

Tsishyn, Matsvei;
Cia, Gabriel;
Hermans, Pauline;
Kwasigroch, Jean;
Rooman, Marianne;
Pucci, Fabrizio

Publication type:

Article

Altered skin microbiome, inflammation, and JAK/STAT signaling in Southeast Asian ichthyosis patients.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00603-x

By:

Ho, Minh;
Nguyen, Huynh-Nga;
Van Hoang, Minh;
Bui, Tien Thuy Thi;
Vu, Bao-Quoc;
Dinh, Truc Huong Thi;
Vo, Hoa Thi My;
Blaydon, Diana C.;
Eldirany, Sherif A.;
Bunick, Christopher G.;
Bui, Chi-Bao

Publication type:

Article

The genetic basis of early-onset hereditary ataxia in Iran: results of a national registry of a heterogeneous population.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00598-5

By:

Mahdieh, Nejat;
Heidari, Morteza;
Rezaei, Zahra;
Tavasoli, Ali Reza;
Hosseinpour, Sareh;
Rasulinejad, Maryam;
Dehnavi, Ali Zare;
Ghahvechi Akbari, Masoud;
Badv, Reza Shervin;
Vafaei, Elahe;
Mohebbi, Ali;
Mohammadi, Pouria;
Hosseiny, Seyyed Mohammad Mahdi;
Azizimalamiri, Reza;
Nikkhah, Ali;
Pourbakhtyaran, Elham;
Rohani, Mohammad;
Khanbanha, Narges;
Nikbakht, Sedigheh;
Movahedinia, Mojtaba

Publication type:

Article

Profiling the role of m6A effectors in the regulation of pluripotent reprogramming.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00597-6

By:

Wang, Wenjun;
Zhou, Lei;
Li, Hui;
Sun, Tingge;
Wen, Xue;
Li, Wei;
Esteban, Miguel A.;
Hoffman, Andrew R.;
Hu, Ji-Fan;
Cui, Jiuwei

Publication type:

Article

Prioritizing susceptibility genes for the prognosis of male-pattern baldness with transcriptome-wide association study.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00591-y

By:

Choi, Eunyoung;
Song, Jaeseung;
Lee, Yubin;
Jeong, Yeonbin;
Jang, Wonhee

Publication type:

Article

Paternal aging impacts expression and epigenetic markers as early as the first embryonic tissue lineage differentiation.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00599-4

By:

Denomme, Michelle M.;
McCallie, Blair R.;
Haywood, Mary E.;
Parks, Jason C.;
Schoolcraft, William B.;
Katz-Jaffe, Mandy G.

Publication type:

Article

Clinical spectrum of Transthyretin amyloidogenic mutations among diverse population origins.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00596-7

By:

De Lillo, Antonella;
Pathak, Gita A.;
Low, Aislinn;
De Angelis, Flavio;
Abou Alaiwi, Sarah;
Miller, Edward J.;
Fuciarelli, Maria;
Polimanti, Renato

Publication type:

Article

Large-scale next generation sequencing based analysis of SLCO1B1 pharmacogenetics variants in the Saudi population.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00594-9

By:

Goljan, Ewa;
Abouelhoda, Mohammed;
Tahir, Asma;
ElKalioby, Mohamed;
Meyer, Brian;
Monies, Dorota

Publication type:

Article

Structural rearrangements as a recurrent pathogenic mechanism for SETBP1 haploinsufficiency.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00600-0

By:

Alesi, V.;
Genovese, S.;
Roberti, M. C.;
Sallicandro, E.;
Di Tommaso, S.;
Loddo, S.;
Orlando, V.;
Pompili, D.;
Calacci, C.;
Mei, V.;
Pisaneschi, E.;
Faggiano, M. V.;
Morgia, A.;
Mammì, C.;
Astrea, G.;
Battini, R.;
Priolo, M.;
Dentici, M. L.;
Milone, R.;
Novelli, A.

Publication type:

Article

Explicable prioritization of genetic variants by integration of rule-based and machine learning algorithms for diagnosis of rare Mendelian disorders.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00595-8

By:

Kim, Ho Heon;
Kim, Dong-Wook;
Woo, Junwoo;
Lee, Kyoungyeul

Publication type:

Article

Hemorrhoidal disease and its genetic association with depression, bipolar disorder, anxiety disorders, and schizophrenia: a bidirectional mendelian randomization study.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00588-7

By:

Huang, Zhiguang;
Huang, Jian;
Leung, Chun Kai;
Zhang, Casper JP;
Akinwunmi, Babatunde;
Ming, Wai-Kit

Publication type:

Article

A genome-wide association study of neutrophil count in individuals associated to an African continental ancestry group facilitates studies of malaria pathogenesis.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00585-w

By:

Constantinescu, Andrei-Emil;
Hughes, David A.;
Bull, Caroline J.;
Fleming, Kathryn;
Mitchell, Ruth E.;
Zheng, Jie;
Kar, Siddhartha;
Timpson, Nicholas J.;
Amulic, Borko;
Vincent, Emma E.

Publication type:

Article

Statistical methods for assessing the effects of de novo variants on birth defects.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00590-z

By:

Xie, Yuhan;
Wu, Ruoxuan;
Li, Hongyu;
Dong, Weilai;
Zhou, Geyu;
Zhao, Hongyu

Publication type:

Article

Altered expression of serum lncRNA CASC2 and miRNA-21-5p in COVID-19 patients.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00578-9

By:

Ayoub, Shymaa E.;
Shaker, Olfat G.;
Masoud, Mohamed;
Hassan, Essam A.;
Ezzat, Eman M.;
Ahmed, Mona I.;
Ahmed, Randa I.;
Amin, Amal A. Ibrahim;
Abd El Reheem, Fadwa;
Khalefa, Abeer A.;
Mahmoud, Rania H.

Publication type:

Article

Cellular and clinical impact of protein phosphatase enzyme epigenetic silencing in multiple cancer tissues.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00592-x

By:

Wiltshire, Edward;
de Moura, Manuel Castro;
Piñeyro, David;
Joshi, Ricky S.

Publication type:

Article

Mutations in TSPAN12 gene causing familial exudative vitreoretinopathy.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00589-6

By:

Ju, Yuqiao;
Chen, Tianhui;
Ruan, Lu;
Zhao, Ye;
Chang, Qing;
Huang, Xin

Publication type:

Article

Combining full-length gene assay and SpliceAI to interpret the splicing impact of all possible SPINK1 coding variants.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00586-9

By:

Wu, Hao;
Lin, Jin-Huan;
Tang, Xin-Ying;
Marenne, Gaëlle;
Zou, Wen-Bin;
Schutz, Sacha;
Masson, Emmanuelle;
Génin, Emmanuelle;
Fichou, Yann;
Le Gac, Gerald;
Férec, Claude;
Liao, Zhuan;
Chen, Jian-Min

Publication type:

Article

Meta-analysis of 46,000 germline de novo mutations linked to human inherited disease.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00587-8

By:

Lopes-Marques, Mónica;
Mort, Matthew;
Carneiro, João;
Azevedo, António;
Amaro, Andreia P.;
Cooper, David N.;
Azevedo, Luísa

Publication type:

Article

Plasma campesterol and ABCG5/ABCG8 gene loci on the risk of cholelithiasis and cholecystitis: evidence from Mendelian randomization and colocalization analyses.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00583-y

By:

Mi, Jiarui;
Jiang, Qingwei;
Qi, Zhengwei;
Liu, Zhengye;
Bai, Xiaoyin;
Zheng, Xia;
Wu, Jiaguo;
Fang, Yanfei;
Yang, Aiming;
Chen, Haotian

Publication type:

Article

Zebrafish as a model to investigate a biallelic gain-of-function variant in MSGN1, associated with a novel skeletal dysplasia syndrome.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00593-w

By:

Koparir, Asuman;
Lekszas, Caroline;
Keseroglu, Kemal;
Rose, Thalia;
Rappl, Lena;
Rad, Aboulfazl;
Maroofian, Reza;
Narendran, Nakul;
Hasanzadeh, Atefeh;
Karimiani, Ehsan Ghayoor;
Boschann, Felix;
Kornak, Uwe;
Klopocki, Eva;
Özbudak, Ertuğrul M.;
Vona, Barbara;
Haaf, Thomas;
Liedtke, Daniel

Publication type:

Article

Protein–protein interaction network-based integration of GWAS and functional data for blood pressure regulation analysis.

Published in:

Human Genomics, 2024, v. 18, p. 1, doi. 10.1186/s40246-023-00565-6

By:

Tsare, Evridiki-Pandora G.;
Klapa, Maria I.;
Moschonas, Nicholas K.

Publication type:

Article

Correction: Association of the C allele of rs479200 in the EGLN1 gene with COVID-19 severity in Indian population: a novel finding.

Published in:

2024

By:

Harit, Renuka;
De, Sajal;
Singh, Piyoosh Kumar;
Kashyap, Deepika;
Kumar, Manish;
Sahu, Dibakar;
Yadav, Chander Prakash;
Mohan, Mradul;
Singh, Vineeta;
Tomar, Ram Singh;
Pandey, Kailash C.;
Vashisht, Kapil

Publication type:

Correction Notice

Gene expression analysis reveals diabetes-related gene signatures.

Published in:

Human Genomics, 2024, v. 18, p. 1, doi. 10.1186/s40246-024-00582-z

By:

Farrim, M. I.;
Gomes, A.;
Milenkovic, D.;
Menezes, R.

Publication type:

Article

A broad wastewater screening and clinical data surveillance for virus-related diseases in the metropolitan Detroit area in Michigan.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00581-0

By:

Li, Yabing;
Miyani, Brijen;
Faust, Russell A.;
David, Randy E.;
Xagoraraki, Irene

Publication type:

Article

Polymorphisms in transcription factor binding sites and enhancer regions and pancreatic ductal adenocarcinoma risk.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00576-x

By:

Ünal, Pelin;
Lu, Ye;
Bueno-de-Mesquita, Bas;
van Eijck, Casper H. J.;
Talar-Wojnarowska, Renata;
Szentesi, Andrea;
Gazouli, Maria;
Kreivenaite, Edita;
Tavano, Francesca;
Małecka-Wojciesko, Ewa;
Erőss, Bálint;
Oliverius, Martin;
Bunduc, Stefania;
Nóbrega Aoki, Mateus;
Vodickova, Ludmila;
Boggi, Ugo;
Giaccherini, Matteo;
Kondrackiene, Jurate;
Chammas, Roger;
Palmieri, Orazio

Publication type:

Article

Causal associations of COVID‐19 on neurosurgical diseases risk: a Mendelian randomization study.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00575-y

By:

Dai, Lirui;
Lyu, Liang;
Zhou, Peizhi;
Jiang, Shu

Publication type:

Article

Wastewater-based epidemiology applied at the building-level reveals distinct virome profiles based on the age of the contributing individuals.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00580-1

By:

Mejías-Molina, Cristina;
Pico-Tomàs, Anna;
Martínez-Puchol, Sandra;
Itarte, Marta;
Torrell, Helena;
Canela, Núria;
Borrego, Carles M.;
Corominas, Lluís;
Rusiñol, Marta;
Bofill-Mas, Sílvia

Publication type:

Article