Works matching IS 1756994X AND DT 2022 AND VI 14 AND IP 1

Results: 163

A one-year genomic investigation of Escherichia coli epidemiology and nosocomial spread at a large US healthcare network.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01150-7
By:
- Mills, Emma G.;
- Martin, Melissa J.;
- Luo, Ting L.;
- Ong, Ana C.;
- Maybank, Rosslyn;
- Corey, Brendan W.;
- Harless, Casey;
- Preston, Lan N.;
- Rosado-Mendez, Joshua A.;
- Preston, Scott B.;
- Kwak, Yoon I.;
- Backlund, Michael G.;
- Bennett, Jason W.;
- Mc Gann, Patrick T.;
- Lebreton, Francois
Publication type:
Article
Neutralization sensitivity, fusogenicity, and infectivity of Omicron subvariants.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01151-6
By:
- Wang, Xue-Jun;
- Yao, Lin;
- Zhang, Hong-Yun;
- Zhu, Ka-Li;
- Zhao, Jing;
- Zhan, Bing-Dong;
- Li, Yi-Ke;
- He, Xue-Juan;
- Huang, Cong;
- Wang, Zhuang-Ye;
- Jiang, Ming-Dong;
- Yang, Peng;
- Yang, Yang;
- Wang, Guo-Lin;
- Wang, Sheng-Qi;
- Dai, Er-Hei;
- Gao, Hui-Xia;
- Ma, Mai-Juan
Publication type:
Article
The role of genetic testing in diagnosis and care of inherited cardiac conditions in a specialised multidisciplinary clinic.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01149-0
By:
- Stafford, Fergus;
- Krishnan, Neesha;
- Richardson, Ebony;
- Butters, Alexandra;
- Hespe, Sophie;
- Burns, Charlotte;
- Gray, Belinda;
- Medi, Caroline;
- Nowak, Natalie;
- Isbister, Julia C.;
- Raju, Hariharan;
- Richmond, David;
- Ryan, Mark P.;
- Singer, Emma S.;
- Sy, Raymond W.;
- Yeates, Laura;
- Bagnall, Richard D.;
- Semsarian, Christopher;
- Ingles, Jodie
Publication type:
Article
Post-vaccine epidemiology of serotype 3 pneumococci identifies transformation inhibition through prophage-driven alteration of a non-coding RNA.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01147-2
By:
- Kwun, Min Jung;
- Ion, Alexandru V.;
- Cheng, Hsueh-Chien;
- D'Aeth, Joshua C.;
- Dougan, Sam;
- Oggioni, Marco R.;
- Goulding, David A.;
- Bentley, Stephen D.;
- Croucher, Nicholas J.
Publication type:
Article
Spatiotemporal evolution of the clear cell renal cell carcinoma microenvironment links intra-tumoral heterogeneity to immune escape.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01146-3
By:
- Golkaram, Mahdi;
- Kuo, Fengshen;
- Gupta, Sounak;
- Carlo, Maria I.;
- Salmans, Michael L.;
- Vijayaraghavan, Raakhee;
- Tang, Cerise;
- Makarov, Vlad;
- Rappold, Phillip;
- Blum, Kyle A.;
- Zhao, Chen;
- Mehio, Rami;
- Zhang, Shile;
- Godsey, Jim;
- Pawlowski, Traci;
- DiNatale, Renzo G.;
- Morris, Luc G. T.;
- Durack, Jeremy;
- Russo, Paul;
- Kotecha, Ritesh R.
Publication type:
Article
Multi-region sequencing with spatial information enables accurate heterogeneity estimation and risk stratification in liver cancer.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01143-6
By:
- Yang, Chen;
- Zhang, Senquan;
- Cheng, Zhuoan;
- Liu, Zhicheng;
- Zhang, Linmeng;
- Jiang, Kai;
- Geng, Haigang;
- Qian, Ruolan;
- Wang, Jun;
- Huang, Xiaowen;
- Chen, Mo;
- Li, Zhe;
- Qin, Wenxin;
- Xia, Qiang;
- Kang, Xiaonan;
- Wang, Cun;
- Hang, Hualian
Publication type:
Article
Calculating variant penetrance from family history of disease and average family size in population-scale data.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01142-7
By:
- Spargo, Thomas P.;
- Opie-Martin, Sarah;
- Bowles, Harry;
- Lewis, Cathryn M.;
- Iacoangeli, Alfredo;
- Al-Chalabi, Ammar
Publication type:
Article
Loss of Y in leukocytes as a risk factor for critical COVID-19 in men.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01144-5
By:
- Bruhn-Olszewska, Bożena;
- Davies, Hanna;
- Sarkisyan, Daniil;
- Juhas, Ulana;
- Rychlicka-Buniowska, Edyta;
- Wójcik, Magdalena;
- Horbacz, Monika;
- Jąkalski, Marcin;
- Olszewski, Paweł;
- Westholm, Jakub O.;
- Smialowska, Agata;
- Wierzba, Karol;
- Torinsson Naluai, Åsa;
- Jern, Niklas;
- Andersson, Lars-Magnus;
- Järhult, Josef D.;
- Filipowicz, Natalia;
- Tiensuu Janson, Eva;
- Rubertsson, Sten;
- Lipcsey, Miklós
Publication type:
Article
Mendelian randomization and genetic colocalization infer the effects of the multi-tissue proteome on 211 complex disease-related phenotypes.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01140-9
By:
- Yang, Chengran;
- Fagan, Anne M.;
- Perrin, Richard J.;
- Rhinn, Herve;
- Harari, Oscar;
- Cruchaga, Carlos
Publication type:
Article
CRAG: de novo characterization of cell-free DNA fragmentation hotspots in plasma whole-genome sequencing.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01141-8
By:
- Zhou, Xionghui;
- Zheng, Haizi;
- Fu, Hailu;
- Dillehay McKillip, Kelsey L.;
- Pinney, Susan M.;
- Liu, Yaping
Publication type:
Article
Therapy sculpts the complex interplay between cancer and the immune system during tumour evolution.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01138-3
By:
- Thol, Kerstin;
- Pawlik, Piotr;
- McGranahan, Nicholas
Publication type:
Article
Cell type-specific changes identified by single-cell transcriptomics in Alzheimer's disease.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01136-5
By:
- Luquez, Tain;
- Gaur, Pallavi;
- Kosater, Ivy M;
- Lam, Matti;
- Lee, Dylan I;
- Mares, Jason;
- Paryani, Fahad;
- Yadav, Archana;
- Menon, Vilas
Publication type:
Article
Epigenetic and transcriptomic reprogramming in monocytes of severe COVID-19 patients reflects alterations in myeloid differentiation and the influence of inflammatory cytokines.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01137-4
By:
- Godoy-Tena, Gerard;
- Barmada, Anis;
- Morante-Palacios, Octavio;
- de la Calle-Fabregat, Carlos;
- Martins-Ferreira, Ricardo;
- Ferreté-Bonastre, Anna G.;
- Ciudad, Laura;
- Ruiz-Sanmartín, Adolfo;
- Martínez-Gallo, Mónica;
- Ferrer, Ricard;
- Ruiz-Rodriguez, Juan Carlos;
- Rodríguez-Ubreva, Javier;
- Vento-Tormo, Roser;
- Ballestar, Esteban
Publication type:
Article
Neutrophil extracellular traps have auto-catabolic activity and produce mononucleosome-associated circulating DNA.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01125-8
By:
- Pisareva, Ekaterina;
- Mihalovičová, Lucia;
- Pastor, Brice;
- Kudriavtsev, Andrei;
- Mirandola, Alexia;
- Mazard, Thibault;
- Badiou, Stephanie;
- Maus, Ulrich;
- Ostermann, Lena;
- Weinmann-Menke, Julia;
- Neuberger, Elmo W. I.;
- Simon, Perikles;
- Thierry, Alain R.
Publication type:
Article
Illuminating links between cis-regulators and trans-acting variants in the human prefrontal cortex.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01133-8
By:
- Liu, Shuang;
- Won, Hyejung;
- Clarke, Declan;
- Matoba, Nana;
- Khullar, Saniya;
- Mu, Yudi;
- Wang, Daifeng;
- Gerstein, Mark
Publication type:
Article
Whole-exome sequencing identifies novel protein-altering variants associated with serum apolipoprotein and lipid concentrations.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01135-6
By:
- Sandholm, Niina;
- Hotakainen, Ronja;
- Haukka, Jani K.;
- Jansson Sigfrids, Fanny;
- Dahlström, Emma H.;
- Antikainen, Anni A.;
- Valo, Erkka;
- Syreeni, Anna;
- Kilpeläinen, Elina;
- Kytölä, Anastasia;
- Palotie, Aarno;
- Harjutsalo, Valma;
- Forsblom, Carol;
- Groop, Per-Henrik
Publication type:
Article
Return of non-ACMG recommended incidental genetic findings to pediatric patients: considerations and opportunities from experiences in genomic sequencing.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01139-2
By:
- Bowling, Kevin M.;
- Thompson, Michelle L.;
- Kelly, Melissa A.;
- Scollon, Sarah;
- Slavotinek, Anne M.;
- Powell, Bradford C.;
- Kirmse, Brian M.;
- Hendon, Laura G.;
- Brothers, Kyle B.;
- Korf, Bruce R.;
- Cooper, Gregory M.;
- Greally, John M.;
- Hurst, Anna C. E.
Publication type:
Article
Extracellular matrix profiles determine risk and prognosis of the squamous cell carcinoma subtype of non-small cell lung carcinoma.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01127-6
By:
- Parker, Amelia L.;
- Bowman, Elise;
- Zingone, Adriana;
- Ryan, Brid M.;
- Cooper, Wendy A.;
- Kohonen-Corish, Maija;
- Harris, Curtis C.;
- Cox, Thomas R.
Publication type:
Article
Towards elucidating disease-relevant states of neurons and glia by CRISPR-based functional genomics.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01134-7
By:
- Leng, Kun;
- Kampmann, Martin
Publication type:
Article
Universal clinical Parkinson's disease axes identify a major influence of neuroinflammation.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01132-9
By:
- Sandor, Cynthia;
- Millin, Stephanie;
- Dahl, Andrew;
- Schalkamp, Ann-Kathrin;
- Lawton, Michael;
- Hubbard, Leon;
- Rahman, Nabila;
- Williams, Nigel;
- Ben-Shlomo, Yoav;
- Grosset, Donald G.;
- Hu, Michele T.;
- Marchini, Jonathan;
- Webber, Caleb
Publication type:
Article
Ganciclovir-induced mutations are present in a diverse spectrum of post-transplant malignancies.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01131-w
By:
- Fang, Hu;
- Yan, Helen H. N.;
- Bilardi, Rebecca A.;
- Flensburg, Christoffer;
- Yang, Haocheng;
- Barbour, Jayne A.;
- Siu, Hoi Cheong;
- Turski, Michelle;
- Chew, Edward;
- Xu, Zhen;
- Lam, Siu T.;
- Sharma, Rakesh;
- Xu, Mengya;
- Li, Junshi;
- Ip, Ho W.;
- Cheung, Carol Y. M.;
- Huen, Michael S. Y.;
- Sweet-Cordero, E. Alejandro;
- Majewski, Ian J.;
- Leung, Suet Y.
Publication type:
Article
Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01106-x
By:
- Johnson, Ruth;
- Ding, Yi;
- Venkateswaran, Vidhya;
- Bhattacharya, Arjun;
- Boulier, Kristin;
- Chiu, Alec;
- Knyazev, Sergey;
- Schwarz, Tommer;
- Freund, Malika;
- Zhan, Lingyu;
- Burch, Kathryn S.;
- Caggiano, Christa;
- Hill, Brian;
- Rakocz, Nadav;
- Balliu, Brunilda;
- Denny, Christopher T.;
- Sul, Jae Hoon;
- Zaitlen, Noah;
- Arboleda, Valerie A.;
- Halperin, Eran
Publication type:
Article
X-CAP improves pathogenicity prediction of stopgain variants.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01078-y
By:
- Rastogi, Ruchir;
- Stenson, Peter D.;
- Cooper, David N.;
- Bejerano, Gill
Publication type:
Article
Genomic and transcriptomic analysis of a diffuse pleural mesothelioma patient-derived xenograft library.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01129-4
By:
- Offin, Michael;
- Sauter, Jennifer L.;
- Tischfield, Sam E.;
- Egger, Jacklynn V.;
- Chavan, Shweta;
- Shah, Nisargbhai S.;
- Manoj, Parvathy;
- Ventura, Katia;
- Allaj, Viola;
- de Stanchina, Elisa;
- Travis, William;
- Ladanyi, Marc;
- Rimner, Andreas;
- Rusch, Valerie W.;
- Adusumilli, Prasad S.;
- Poirier, John T.;
- Zauderer, Marjorie G.;
- Rudin, Charles M.;
- Sen, Triparna
Publication type:
Article
Network reconstruction for trans acting genetic loci using multi-omics data and prior information.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01124-9
By:
- Hawe, Johann S.;
- Saha, Ashis;
- Waldenberger, Melanie;
- Kunze, Sonja;
- Wahl, Simone;
- Müller-Nurasyid, Martina;
- Prokisch, Holger;
- Grallert, Harald;
- Herder, Christian;
- Peters, Annette;
- Strauch, Konstantin;
- Theis, Fabian J.;
- Gieger, Christian;
- Chambers, John;
- Battle, Alexis;
- Heinig, Matthias
Publication type:
Article
Author Correction: Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative.
Published in:
2022
By:
- Johnson, Ruth;
- Ding, Yi;
- Venkateswaran, Vidhya;
- Bhattacharya, Arjun;
- Boulier, Kristin;
- Chiu, Alec;
- Knyazev, Sergey;
- Schwarz, Tommer;
- Freund, Malika;
- Zhan, Lingyu;
- Burch, Kathryn S.;
- Caggiano, Christa;
- Hill, Brian;
- Rakocz, Nadav;
- Balliu, Brunilda;
- Denny, Christopher T.;
- Sul, Jae Hoon;
- Zaitlen, Noah;
- Arboleda, Valerie A.;
- Halperin, Eran
Publication type:
Correction Notice
Application of exome sequencing for prenatal diagnosis of fetal structural anomalies: clinical experience and lessons learned from a cohort of 1618 fetuses.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01130-x
By:
- Fu, Fang;
- Li, Ru;
- Yu, Qiuxia;
- Wang, Dan;
- Deng, Qiong;
- Li, Lushan;
- Lei, Tingying;
- Chen, Guilan;
- Nie, Zhiqiang;
- Yang, Xin;
- Han, Jin;
- Pan, Min;
- Zhen, Li;
- Zhang, Yongling;
- Jing, Xiangyi;
- Li, Fucheng;
- Li, Fatao;
- Zhang, Lina;
- Yi, Cuixing;
- Li, Yingsi
Publication type:
Article
The lung microbiome, peripheral gene expression, and recurrence-free survival after resection of stage II non-small cell lung cancer.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01126-7
By:
- Peters, Brandilyn A.;
- Pass, Harvey I.;
- Burk, Robert D.;
- Xue, Xiaonan;
- Goparaju, Chandra;
- Sollecito, Christopher C.;
- Grassi, Evan;
- Segal, Leopoldo N.;
- Tsay, Jun-Chieh J.;
- Hayes, Richard B.;
- Ahn, Jiyoung
Publication type:
Article
The multiple de novo copy number variant (MdnCNV) phenomenon presents with peri-zygotic DNA mutational signatures and multilocus pathogenic variation.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01123-w
By:
- Du, Haowei;
- Jolly, Angad;
- Grochowski, Christopher M.;
- Yuan, Bo;
- Dawood, Moez;
- Jhangiani, Shalini N.;
- Li, He;
- Muzny, Donna;
- Fatih, Jawid M.;
- Coban-Akdemir, Zeynep;
- Carlin, Mary Esther;
- Scheuerle, Angela E.;
- Witzl, Karin;
- Posey, Jennifer E.;
- Pendleton, Matthew;
- Harrington, Eoghan;
- Juul, Sissel;
- Hastings, P. J.;
- Bi, Weimin;
- Gibbs, Richard A.
Publication type:
Article
Computational quantification and characterization of independently evolving cellular subpopulations within tumors is critical to inhibit anti-cancer therapy resistance.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01121-y
By:
- Alkhatib, Heba;
- Rubinstein, Ariel M.;
- Vasudevan, Swetha;
- Flashner-Abramson, Efrat;
- Stefansky, Shira;
- Chowdhury, Sangita Roy;
- Oguche, Solomon;
- Peretz-Yablonsky, Tamar;
- Granit, Avital;
- Granot, Zvi;
- Ben-Porath, Ittai;
- Sheva, Kim;
- Feldman, Jon;
- Cohen, Noa E.;
- Meirovitz, Amichay;
- Kravchenko-Balasha, Nataly
Publication type:
Article
DNA methylome-wide association study of genetic risk for depression implicates antigen processing and immune responses.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01039-5
By:
- Shen, Xueyi;
- Caramaschi, Doretta;
- Adams, Mark J.;
- Walker, Rosie M.;
- Min, Josine L.;
- Kwong, Alex;
- Hemani, Gibran;
- Barbu, Miruna C.;
- Whalley, Heather C.;
- Harris, Sarah E.;
- Deary, Ian J.;
- Morris, Stewart W.;
- Cox, Simon R.;
- Relton, Caroline L.;
- Marioni, Riccardo E.;
- Evans, Kathryn L.;
- McIntosh, Andrew M.
Publication type:
Article
The WID-CIN test identifies women with, and at risk of, cervical intraepithelial neoplasia grade 3 and invasive cervical cancer.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01116-9
By:
- Barrett, James E.;
- Sundström, Karin;
- Jones, Allison;
- Evans, Iona;
- Wang, Jiangrong;
- Herzog, Chiara;
- Dillner, Joakim;
- Widschwendter, Martin
Publication type:
Article
CTpathway: a CrossTalk-based pathway enrichment analysis method for cancer research.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01119-6
By:
- Liu, Haizhou;
- Yuan, Mengqin;
- Mitra, Ramkrishna;
- Zhou, Xu;
- Long, Min;
- Lei, Wanyue;
- Zhou, Shunheng;
- Huang, Yu-e;
- Hou, Fei;
- Eischen, Christine M.;
- Jiang, Wei
Publication type:
Article
Mendelian gene identification through mouse embryo viability screening.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01118-7
By:
- Cacheiro, Pilar;
- Westerberg, Carl Henrik;
- Mager, Jesse;
- Dickinson, Mary E.;
- Nutter, Lauryl M. J.;
- Muñoz-Fuentes, Violeta;
- Hsu, Chih-Wei;
- Van den Veyver, Ignatia B.;
- Flenniken, Ann M.;
- McKerlie, Colin;
- Murray, Stephen A.;
- Teboul, Lydia;
- Heaney, Jason D.;
- Lloyd, K. C. Kent;
- Lanoue, Louise;
- Braun, Robert E.;
- White, Jacqueline K.;
- Creighton, Amie K.;
- Laurin, Valerie;
- Guo, Ruolin
Publication type:
Article
Correction: Elucidating the diversity of malignant mesenchymal states in glioblastoma by integrative analysis.
Published in:
2022
By:
- Chanoch-Myers, Rony;
- Wider, Adi;
- Suva, Mario L.;
- Tirosh, Itay
Publication type:
Correction Notice
MetaRNN: differentiating rare pathogenic and rare benign missense SNVs and InDels using deep learning.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01120-z
By:
- Li, Chang;
- Zhi, Degui;
- Wang, Kai;
- Liu, Xiaoming
Publication type:
Article
Patient and provider perspectives on polygenic risk scores: implications for clinical reporting and utilization.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01117-8
By:
- Lewis, Anna C. F.;
- Perez, Emma F.;
- Prince, Anya E. R.;
- Flaxman, Hana R.;
- Gomez, Lizbeth;
- Brockman, Deanna G.;
- Chandler, Paulette D.;
- Kerman, Benjamin J.;
- Lebo, Matthew S.;
- Smoller, Jordan W.;
- Weiss, Scott T.;
- Blout Zawatksy, Carrie L.;
- Meigs, James B.;
- Green, Robert C.;
- Vassy, Jason L.;
- Karlson, Elizabeth W.
Publication type:
Article
Sequencing individual genomes with recurrent genomic disorder deletions: an approach to characterize genes for autosomal recessive rare disease traits.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01113-y
By:
- Yuan, Bo;
- Schulze, Katharina V.;
- Assia Batzir, Nurit;
- Sinson, Jefferson;
- Dai, Hongzheng;
- Zhu, Wenmiao;
- Bocanegra, Francia;
- Fong, Chin-To;
- Holder, Jimmy;
- Nguyen, Joanne;
- Schaaf, Christian P.;
- Yang, Yaping;
- Bi, Weimin;
- Eng, Christine;
- Shaw, Chad;
- Lupski, James R.;
- Liu, Pengfei
Publication type:
Article
African-specific alleles modify risk for asthma at the 17q12-q21 locus in African Americans.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01114-x
By:
- Washington III, Charles;
- Dapas, Matthew;
- Biddanda, Arjun;
- Magnaye, Kevin M.;
- Aneas, Ivy;
- Helling, Britney A.;
- Szczesny, Brooke;
- Boorgula, Meher Preethi;
- Taub, Margaret A.;
- Kenny, Eimear;
- Mathias, Rasika A.;
- Barnes, Kathleen C.;
- CAAPA;
- Campbell, Monica;
- Figueiredo, Camila;
- Hansel, Nadia N.;
- Ober, Carole;
- Olopade, Christopher O.;
- Rotimi, Charles N.;
- Watson, Harold
Publication type:
Article
Transcriptional signatures of the BCL2 family for individualized acute myeloid leukaemia treatment.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01115-w
By:
- Lee, Chansub;
- Lee, Sungyoung;
- Park, Eunchae;
- Hong, Junshik;
- Shin, Dong-Yeop;
- Byun, Ja Min;
- Yun, Hongseok;
- Koh, Youngil;
- Yoon, Sung-Soo
Publication type:
Article
Longitudinal multi-omics analysis identifies early blood-based predictors of anti-TNF therapy response in inflammatory bowel disease.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01112-z
By:
- Mishra, Neha;
- Aden, Konrad;
- Blase, Johanna I.;
- Baran, Nathan;
- Bordoni, Dora;
- Tran, Florian;
- Conrad, Claudio;
- Avalos, Diana;
- Jaeckel, Charlot;
- Scherer, Michael;
- Sørensen, Signe B.;
- Overgaard, Silja H.;
- Schulte, Berenice;
- Nikolaus, Susanna;
- Rey, Guillaume;
- Gasparoni, Gilles;
- Lyons, Paul A.;
- Schultze, Joachim L.;
- Walter, Jörn;
- Andersen, Vibeke
Publication type:
Article
Single-cell RNA transcriptome analysis of CNS immune cells reveals CXCL16/CXCR6 as maintenance factors for tissue-resident T cells that drive synapse elimination.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01111-0
By:
- Rosen, Sarah F.;
- Soung, Allison L.;
- Yang, Wei;
- Ai, Shenjian;
- Kanmogne, Marlene;
- Davé, Veronica A.;
- Artyomov, Maxim;
- Magee, Jeffrey A.;
- Klein, Robyn S.
Publication type:
Article
Intratumor heterogeneity and T cell exhaustion in primary CNS lymphoma.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01110-1
By:
- Heming, Michael;
- Haessner, Svea;
- Wolbert, Jolien;
- Lu, I-Na;
- Li, Xiaolin;
- Brokinkel, Benjamin;
- Müther, Michael;
- Holling, Markus;
- Stummer, Walter;
- Thomas, Christian;
- Schulte-Mecklenbeck, Andreas;
- de Faria, Flavia;
- Stoeckius, Marlon;
- Hailfinger, Stephan;
- Lenz, Georg;
- Kerl, Kornelius;
- Wiendl, Heinz;
- Meyer zu Hörste, Gerd;
- Grauer, Oliver M.
Publication type:
Article
Correction: Rapid molecular diagnostics of tuberculosis resistance by targeted stool sequencing.
Published in:
2022
By:
- Sibandze, Doctor B.;
- Kay, Alexander;
- Dreyer, Viola;
- Sikhondze, Welile;
- Dlamini, Qiniso;
- DiNardo, Andrew;
- Mtetwa, Godwin;
- Lukhele, Bhekumusa;
- Vambe, Debrah;
- Lange, Christoph;
- Dlamini, Muyalo Glenn;
- Ness, Tara;
- Mejia, Rojelio;
- Kalsdorf, Barbara;
- Heyckendorf, Jan;
- Kuhns, Martin;
- Maurer, Florian P.;
- Dlamini, Sindisiwe;
- Maphalala, Gugu;
- Niemann, Stefan
Publication type:
Correction Notice
Elucidating the diversity of malignant mesenchymal states in glioblastoma by integrative analysis.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01109-8
By:
- Chanoch-Myers, Rony;
- Wider, Adi;
- Suva, Mario L.;
- Tirosh, Itay
Publication type:
Article
A novel molecular signature identifies mixed subtypes in renal cell carcinoma with poor prognosis and independent response to immunotherapy.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01105-y
By:
- Büttner, Florian A.;
- Winter, Stefan;
- Stühler, Viktoria;
- Rausch, Steffen;
- Hennenlotter, Jörg;
- Füssel, Susanne;
- Zastrow, Stefan;
- Meinhardt, Matthias;
- Toma, Marieta;
- Jerónimo, Carmen;
- Henrique, Rui;
- Miranda-Gonçalves, Vera;
- Kröger, Nils;
- Ribback, Silvia;
- Hartmann, Arndt;
- Agaimy, Abbas;
- Stöhr, Christine;
- Polifka, Iris;
- Fend, Falko;
- Scharpf, Marcus
Publication type:
Article
Single-cell transcriptomics reveals common epithelial response patterns in human acute kidney injury.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01108-9
By:
- Hinze, Christian;
- Kocks, Christine;
- Leiz, Janna;
- Karaiskos, Nikos;
- Boltengagen, Anastasiya;
- Cao, Shuang;
- Skopnik, Christopher Mark;
- Klocke, Jan;
- Hardenberg, Jan-Hendrik;
- Stockmann, Helena;
- Gotthardt, Inka;
- Obermayer, Benedikt;
- Haghverdi, Laleh;
- Wyler, Emanuel;
- Landthaler, Markus;
- Bachmann, Sebastian;
- Hocke, Andreas C.;
- Corman, Victor;
- Busch, Jonas;
- Schneider, Wolfgang
Publication type:
Article
Integrative genomic and transcriptomic analyses illuminate the ontology of HER2-low breast carcinomas.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01104-z
By:
- Berrino, Enrico;
- Annaratone, Laura;
- Bellomo, Sara Erika;
- Ferrero, Giulio;
- Gagliardi, Amedeo;
- Bragoni, Alberto;
- Grassini, Dora;
- Guarrera, Simonetta;
- Parlato, Caterina;
- Casorzo, Laura;
- Panero, Mara;
- Sarotto, Ivana;
- Giordano, Silvia;
- Cereda, Matteo;
- Montemurro, Filippo;
- Ponzone, Riccardo;
- Crosetto, Nicola;
- Naccarati, Alessio;
- Sapino, Anna;
- Marchiò, Caterina
Publication type:
Article
Accumulation of copy number alterations and clinical progression across advanced prostate cancer.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01080-4
By:
- Grist, Emily;
- Friedrich, Stefanie;
- Brawley, Christopher;
- Mendes, Larissa;
- Parry, Marina;
- Ali, Adnan;
- Haran, Aine;
- Hoyle, Alex;
- Gilson, Claire;
- Lall, Sharanpreet;
- Zakka, Leila;
- Bautista, Carla;
- Landless, Alex;
- Nowakowska, Karolina;
- Wingate, Anna;
- Wetterskog, Daniel;
- Hasan, A. M. Mahedi;
- Akato, Nafisah B.;
- Richmond, Malissa;
- Ishaq, Sofeya
Publication type:
Article
Genome-wide interrogation of structural variation reveals novel African-specific prostate cancer oncogenic drivers.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01096-w
By:
- Gong, Tingting;
- Jaratlerdsiri, Weerachai;
- Jiang, Jue;
- Willet, Cali;
- Chew, Tracy;
- Patrick, Sean M.;
- Lyons, Ruth J.;
- Haynes, Anne-Maree;
- Pasqualim, Gabriela;
- Brum, Ilma Simoni;
- Stricker, Phillip D.;
- Mutambirwa, Shingai B. A.;
- Sadsad, Rosemarie;
- Papenfuss, Anthony T.;
- Bornman, Riana M. S.;
- Chan, Eva K. F.;
- Hayes, Vanessa M.
Publication type:
Article