HuGE Literature Finder
Records 1-30
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The Prognostic Ability of RAS Pathway-Related Gene Mutations in Patients with Myeloid Neoplasms Treated with Hypomethylating Agents.
Acta haematologica 2021 Jul 1-11. Park Hee Sue, Son Bo Ra, Shin Kyeong Seob, Byeon Seonggyu, Kim Hee Kyung, Yang Yaewon, Jeong Yusook, Han Hye Sook, Lee Ki Hyeong, Kwon Jihy |
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Clinical implications of copy number alteration detection using panel-based next-generation sequencing data in myelodysplastic syndrome.
Leukemia research 2021 Apr 103 106540. Kim Yoo-Jin, Jung Seung-Hyun, Hur Eun-Hye, Choi Eun-Ji, Lee Kyoo-Hyung, Park Hyeon-Chun, Kim Hye Joung, Kwon Yong-Rim, Park Silvia, Lee Sug Hyung, Chung Yeun-Jun, Lee Je-Hw |
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Genetic alterations in Thai adult patients with acute myeloid leukemia and myelodysplastic syndrome-excess blasts detected by next-generation sequencing technique.
Annals of hematology 2021 Apr . Owattanapanich Weerapat, Herzig Julia, Jahn Nikolaus, Panina Ekaterina, Ruchutrakool Theera, Kungwankiattichai Smith, Issaragrisil Surapol, Döhner Hartmut, Döhner Konstan |
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Pediatric Non-Alcoholic Fatty Liver Disease is Affected by Genetic Variants Involved in Lifespan/Healthspan.
Journal of pediatric gastroenterology and nutrition 2021 Mar . Crudele Annalisa, Dato Serena, Re Oriana Lo, Maugeri Andrea, Sanna Paola, Giallongo Sebastiano, Oben Jude, Panera Nadia, De Rango Francesco, Mosca Antonella, Rose Giuseppina, Passarino Giuseppe, Alisi Anna, Vinciguerra Manl |
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Whole Exome Sequencing in BRCA1-2 Candidate Families: The Contribution of Other Cancer Susceptibility Genes.
Frontiers in oncology 2021 11 649435. Doddato Gabriella, Valentino Floriana, Giliberti Annarita, Papa Filomena Tiziana, Tita Rossella, Bruno Lucia Pia, Resciniti Sara, Fallerini Chiara, Benetti Elisa, Palmieri Maria, Mencarelli Maria Antonietta, Fabbiani Alessandra, Bruttini Mirella, Orrico Alfredo, Baldassarri Margherita, Fava Francesca, Lopergolo Diego, Lo Rizzo Caterina, Lamacchia Vittoria, Mannucci Sara, Pinto Anna Maria, Curr Aurora, Mancini Virginia, , , Mari Francesca, Renieri Alessandra, Ariani Frances |
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Panel gene profiling of small bowel adenocarcinoma: Results from the NADEGE prospective cohort.
International journal of cancer 2020 Nov . Aparicio Thomas, Svrcek Magali, Henriques Julie, Afchain Pauline, Lièvre Astrid, Tougeron David, Gagniere Johan, Terrebonne Eric, Piessen Guillaume, Legoux Jean-Louis, Lecaille Cédric, Pocard Marc, Gornet Jean-Marc, Zaanan Aziz, Lavau-Denes Sandrine, Lecomte Thierry, Deutsch David, Vernerey Dewi, Laurent Puig Pier |
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ASXL1 mutation as a surrogate marker in acute myeloid leukemia with myelodysplasia-related changes and normal karyotype.
Cancer medicine 2020 Mar . Prats-Martín Concepción, Burillo-Sanz Sergio, Morales-Camacho Rosario M, Pérez-López Olga, Suito Milagros, Vargas Maria T, Caballero-Velázquez Teresa, Carrillo-Cruz Estrella, González José, Bernal Ricardo, Pérez-Simón José |
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Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in Patients With Osteosarcoma.
JAMA oncology 2020 Mar . Mirabello Lisa, Zhu Bin, Koster Roelof, Karlins Eric, Dean Michael, Yeager Meredith, Gianferante Matthew, Spector Logan G, Morton Lindsay M, Karyadi Danielle, Robison Leslie L, Armstrong Gregory T, Bhatia Smita, Song Lei, Pankratz Nathan, Pinheiro Maisa, Gastier-Foster Julie M, Gorlick Richard, de Toledo Silvia Regina Caminada, Petrilli Antonio S, Patino-Garcia Ana, Lecanda Fernando, Gutierrez-Jimeno Miriam, Serra Massimo, Hattinger Claudia, Picci Piero, Scotlandi Katia, Flanagan Adrienne M, Tirabosco Roberto, Amary Maria Fernanda, Kurucu Nilgün, Ilhan Inci Ergurhan, Ballinger Mandy L, Thomas David M, Barkauskas Donald A, Mejia-Baltodano Gerardo, Valverde Patricia, Hicks Belynda D, Zhu Bin, Wang Mingyi, Hutchinson Amy A, Tucker Margaret, Sampson Joshua, Landi Maria T, Freedman Neal D, Gapstur Susan, Carter Brian, Hoover Robert N, Chanock Stephen J, Savage Sharon |
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A 4-gene leukemic stem cell score can independently predict the prognosis of myelodysplastic syndrome patients.
Blood advances 2020 Feb 4 (4): 644-654. Wang Yu-Hung, Lin Chien-Chin, Yao Chi-Yuan, Hsu Chia-Lang, Hou Hsin-An, Tsai Cheng-Hong, Chou Wen-Chien, Tien Hwei-Fa |
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Genomic context and TP53 allele frequency define clinical outcomes in TP53-mutated myelodysplastic syndromes.
Blood advances 2020 Feb 4 (3): 482-495. Montalban-Bravo Guillermo, Kanagal-Shamanna Rashmi, Benton Christopher B, Class Caleb A, Chien Kelly S, Sasaki Koji, Naqvi Kiran, Alvarado Yesid, Kadia Tapan M, Ravandi Farhad, Daver Naval, Takahashi Koichi, Jabbour Elias, Borthakur Gautham, Pemmaraju Naveen, Konopleva Marina, Soltysiak Kelly A, Pierce Sherry R, Bueso-Ramos Carlos E, Patel Keyur P, Kantarjian Hagop, Garcia-Manero Guiller |
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Germline variants in DNA repair genes associated with hereditary breast and ovarian cancer syndrome: analysis of a 21 gene panel in the Brazilian population.
BMC medical genomics 2020 Feb 13 (1): 21. da Costa E Silva Carvalho Simone, Cury Nathalia Moreno, Brotto Danielle Barbosa, de Araujo Luiza Ferreira, Rosa Reginaldo Cruz Alves, Texeira Lorena Alves, Plaça Jessica Rodrigues, Marques Adriana Aparecida, Peronni Kamila Chagas, Ruy Patricia de Cássia, Molfetta Greice Andreotti, Moriguti Julio Cesar, Carraro Dirce Maria, Palmero Edenir Inêz, Ashton-Prolla Patricia, de Faria Ferraz Victor Evangelista, Silva Wilson Arau |
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Germline Profiling and Molecular Characterization of Early Onset Metastatic Colorectal Cancer.
Frontiers in oncology 2020 10 568911. Xu Ting, Zhang Yinjie, Zhang Jing, Qi Changsong, Liu Dan, Wang Zhenghang, Li Yanyan, Ji Congcong, Li Jian, Lin Xuan, Hou Ting, Liu Hao, Zhang Lu, Han-Zhang Han, Shen Lin, Wang Xiche |
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Identification of germline pathogenic variants in DNA damage repair genes by a next-generation sequencing multigene panel in BRCAX patients.
Clinical biochemistry 2019 Nov . Rodríguez-Balada Marta, Roig Bàrbara, Melé Mireia, Albacar Cinta, Serrano Sara, Salvat Mònica, Querol Montserrat, Borràs Joan, Martorell Lourdes, Gumà Jos |
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MIR605 rs2043556 is associated with the occurrence of multiple primary tumors in TP53 p.(Arg337His) mutation carriers.
Cancer genetics 2019 Nov 240 54-58. Bandeira Isabel Cristina, Vieira Igor Araujo, Andreis Tiago Finger, Brussa Reis Larissa, Macedo Gabriel S, Vianna Fernanda Sales Luiz, Santos-Silva Patricia, Palmero Edenir Inez, Galvão Henrique de Campos Reis, Ramos Cintia Regina Niederauer, Santiago Karina Miranda, Achatz Maria Isabel, da Costa Alexandre André Balieiro Anastácio, Ashton-Prolla Patric |
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Radiotherapy-induced malignancies in breast cancer patients with TP53 pathogenic germline variants (Li-Fraumeni syndrome).
Familial cancer 2019 Nov . Petry Vanessa, Bonadio Renata Colombo, Cagnacci Allyne Queiroz Carneiro, Senna Luiz Antonio Leite, Campos Roberta do Nascimento Galvão, Cotti Guilherme Cutait, Hoff Paulo M, Fragoso Maria Candida Barisson Villares, Estevez-Diz Maria Del Pil |
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Tissue-specific microRNA expression alters cancer susceptibility conferred by a TP53 noncoding variant.
Nature communications 2019 Nov 10 (1): 5061. Deng Qipan, Hu Hui, Yu Xinfang, Liu Shuanglin, Wang Lei, Chen Weiqun, Zhang Chi, Zeng Zhaoyang, Cao Ya, Xu-Monette Zijun Y, Li Ling, Zhang Mingzhi, Rosenfeld Steven, Bao Shideng, Hsi Eric, Young Ken H, Lu Zhongxin, Li Yo |
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A substantial proportion of apparently heterozygous TP53 pathogenic variants detected with a next-generation sequencing hereditary pan-cancer panel are acquired somatically.
Human mutation 2019 Sep . Coffee Bradford, Cox Hannah C, Bernhisel Ryan, Manley Susan, Bowles Karla, Roa Benjamin B, Mancini-DiNardo Debo |
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The diagnostic utility of targeted gene panel sequencing in discriminating etiologies of cytopenia.
American journal of hematology 2019 Jul . Zheng Gang, Chen Ping, Pallavajjalla Aparna, Haley Lisa, Gondek Lukasz, Dezern Amy, Ling Hua, De Marchi Federico, Lin Ming-Tseh, Gocke Christoph |
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The molecular genetic make-up of male breast cancer.
Endocrine-related cancer 2019 Jul . Moelans Cathy B, de Ligt Joep, van der Groep Petra, Prins Pjotr, Besselink Nicolle, Hoogstraat Marlous, Ter Hoeve Natalie, Lacle Miangela, Kornegoor Robert, van der Pol Carmen, de Leng Wendy, Barbe Ellis, van der Vegt Bert, Martens John, Bult Peter, Smits Vincent Thbm, Koudijs Marco, Nijman Isaac, Voest Emile, Selenica Pier, Weigelt Britta, Reis-Filho Jorge, van der Wall Elsken, Cuppen Edwin, van Diest Paul |
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[Clinical Characteristics and Karyotype Analysis of Myelodysplastic Syndrome Patients with TP53 mutation].
Zhongguo shi yan xue ye xue za zhi 2019 Jun 27 (3): 872-876. Zhou Xu-Yan, Ouyang Gui-Fang, Mu Qi-Tian, Sheng Li-X |
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Prevalence of germline mutations in the TP53 gene in patients with early-onset breast cancer in the Mexican population.
BMC cancer 2019 Feb 19 (1): 118. Gallardo-Alvarado Lenny N, Tusié-Luna María Teresa, Tussié-Luna María Isabel, Díaz-Chávez José, Segura Yayoi X, Bargallo-Rocha Enrique, Villarreal Cynthia, Herrera-Montalvo Luis A, Herrera-Medina Enrique M, Cantu-de Leon David |
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Genetic and transcriptional landscape of plasma cells in POEMS syndrome.
Leukemia 2019 Jan . Nagao Yuhei, Mimura Naoya, Takeda June, Yoshida Kenichi, Shiozawa Yusuke, Oshima Motohiko, Aoyama Kazumasa, Saraya Atsunori, Koide Shuhei, Rizq Ola, Hasegawa Yoshinori, Shiraishi Yuichi, Chiba Kenichi, Tanaka Hiroko, Nishijima Dai, Isshiki Yusuke, Kayamori Kensuke, Kawajiri-Manako Chika, Oshima-Hasegawa Nagisa, Tsukamoto Shokichi, Mitsukawa Shio, Takeda Yusuke, Ohwada Chikako, Takeuchi Masahiro, Iseki Tohru, Misawa Sonoko, Miyano Satoru, Ohara Osamu, Yokote Koutaro, Sakaida Emiko, Kuwabara Satoshi, Sanada Masashi, Iwama Atsushi, Ogawa Seishi, Nakaseko Chia |
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Diagnostic yield and clinical utility of a comprehensive gene panel for hereditary tumor syndromes.
Hereditary cancer in clinical practice 2019 17 5. Henn Jonas, Spier Isabel, Adam Ronja S, Holzapfel Stefanie, Uhlhaas Siegfried, Kayser Katrin, Plotz Guido, Peters Sophia, Aretz Stef |
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Clinical outcomes of adolescents and young adults with advanced solid tumours participating in phase I trials.
European journal of cancer (Oxford, England : 1990) 2018 Sep 101 55-61. Sundar Raghav, McVeigh Terri, Dolling David, Petruckevitch Ann, Diamantis Nikolaos, Ang Joo Ern, Chenard-Poiriér Maxime, Collins Dearbhaile, Lim Joline, Ameratunga Malaka, Khan Khurum, Kaye Stan B, Banerji Udai, Lopez Juanita, George Angela J, de Bono Johann S, van der Graaf Winette |
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Diagnosis of Li-Fraumeni Syndrome: Differentiating TP53 germline mutations from clonal hematopoiesis: Results of the observational AGO-TR1 trial.
Human mutation 2018 Sep . Weber-Lassalle Konstantin, Harter Philipp, Hauke Jan, Ernst Corinna, Kommoss Stefan, Marmé Frederik, Weber-Lassalle Nana, Prieske Katharina, Dietrich Dimo, Borde Julika, Pohl-Rescigno Esther, Reuss Alexander, Ataseven Beyhan, Engel Christoph, Stingl Julia C, Schmutzler Rita K, Hahnen Er |
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Breast cancer patients suggestive of Li-Fraumeni syndrome: mutational spectrum, candidate genes, and unexplained heredity.
Breast cancer research : BCR 2018 Aug 20 (1): 87. Penkert Judith, Schmidt Gunnar, Hofmann Winfried, Schubert Stephanie, Schieck Maximilian, Auber Bernd, Ripperger Tim, Hackmann Karl, Sturm Marc, Prokisch Holger, Hille-Betz Ursula, Mark Dorothea, Illig Thomas, Schlegelberger Brigitte, Steinemann Dor |
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Targeted Genomic Profiling of Female Adnexal Tumors of Probable Wolffian Origin (FATWO).
International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists 2018 Aug . Mirkovic Jelena, Dong Fei, Sholl Lynette M, Garcia Elizabeth, Lindeman Neal, MacConaill Laura, Crum Christopher P, Nucci Marisa R, McCluggage W Glenn, Howitt Brooke |
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Clinical genetic testing outcome with multi-gene panel in Asian patients with multiple primary cancers.
Oncotarget 2018 Jul 9 (55): 30649-30660. Chan Gloria H J, Ong Pei Yi, Low Jeffrey J H, Kong Hwai Loong, Ow Samuel G W, Tan David S P, Lim Yi Wan, Lim Siew Eng, Lee Soo-Ch |
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Association of Single-Nucleotide Polymorphisms in Monoubiquitinated FANCD2-DNA Damage Repair Pathway Genes With Breast Cancer in the Chinese Population.
Technology in cancer research & treatment 2018 Jan 17 1533033818819841. Chen Fei-Yu, Wang Hao, Li Hui, Hu Xue-Li, Dai Xu, Wang Shou-Man, Yan Guo-Jiao, Jiang Ping-Lan, Hu Yuan-Ping, Huang Juan, Tang Li- |
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TP53 mutation in allogeneic hematopoietic cell transplantation for de novo myelodysplastic syndrome.
Leukemia research 2018 11 74 97-104. Kim Yoo-Jin, Jung Seung-Hyun, Hur Eun-Hye, Choi Eun-Ji, Lee Kyoo-Hyung, Yim Seon-Hee, Kim Hye-Jung, Kwon Yong-Rim, Jeon Young-Woo, Lee Sug Hyung, Chung Yeun-Jun, Lee Je-Hw |
- Page last reviewed:Oct 1, 2020
- Page last updated:Sep 16, 2021
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