Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 63 Records) |
Query Trace: NSD1[original query] |
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Mutated WT1, FLT3-ITD, and NUP98-NSD1 Fusion in Various Combinations Define a Poor Prognostic Group in Pediatric Acute Myeloid Leukemia. Journal of oncology 2019 8 2019 1609128. Niktoreh Naghmeh, Walter Christiane, Zimmermann Martin, von Neuhoff Christine, von Neuhoff Nils, Rasche Mareike, Waack Katharina, Creutzig Ursula, Hanenberg Helmut, Reinhardt Di |
Genetic investigation of patients with tall stature. European journal of endocrinology 2019 Nov . Vasco de Albuquerque Albuquerque Edoarda, Ferreira de Assis Funari Mariana, Pereira de Souza Quedas Elisângela, Sayuri Honjo Kawahira Rachel, Soares Jallad Raquel, Homma Thaís Kataoka, Martin Regina Matsunaga, Brito Vinicius Nahime, Malaquias Alexsandra Christianne, Lerario Antonio Marcondes, Rosenberg Carla, Victorino Krepischi Ana Cristina, Ae Kim Chong, Arnhold Ivo Jorge Prado, Jorge Alexander Augusto de Li |
Neurological disorder-associated genetic variants in individuals with psychogenic nonepileptic seizures. Scientific reports 2020 9 10 (1): 15205. Leu Costin, Bautista Jocelyn F, Sudarsanam Monica, Niestroj Lisa-Marie, Stefanski Arthur, Ferguson Lisa, Daly Mark J, Jehi Lara, Najm Imad M, Busch Robyn M, Lal Denn |
Integrated genomic analysis reveals mutated ELF3 as a potential gallbladder cancer vaccine candidate. Nature communications 2020 8 11 (1): 4225. Pandey Akhilesh, Stawiski Eric W, Durinck Steffen, Gowda Harsha, Goldstein Leonard D, Barbhuiya Mustafa A, Schröder Markus S, Sreenivasamurthy Sreelakshmi K, Kim Sun-Whe, Phalke Sameer, Suryamohan Kushal, Lee Kayla, Chakraborty Papia, Kode Vasumathi, Shi Xiaoshan, Chatterjee Aditi, Datta Keshava, Khan Aafaque A, Subbannayya Tejaswini, Wang Jing, Chaudhuri Subhra, Gupta Sanjiv, Shrivastav Braj Raj, Jaiswal Bijay S, Poojary Satish S, Bhunia Shushruta, Garcia Patricia, Bizama Carolina, Rosa Lorena, Kwon Wooil, Kim Hongbeom, Han Youngmin, Yadav Thakur Deen, Ramprasad Vedam L, Chaudhuri Amitabha, Modrusan Zora, Roa Juan Carlos, Tiwari Pramod Kumar, Jang Jin-Young, Seshagiri Somasek |
DNA Methylation Profiling and Genomic Analysis in 20 Children with Short Stature Who Were Born Small for Gestational Age. The Journal of clinical endocrinology and metabolism 2020 7 105 (12): . Peeters Silke, Declerck Ken, Thomas Muriel, Boudin Eveline, Beckers Dominique, Chivu Olimpia, Heinrichs Claudine, Devriendt Koenraad, de Zegher Francis, Van Hul Wim, Vanden Berghe Wim, De Schepper Jean, Rooman Raoul, Mortier Geert, |
Common variation of the NSD1 gene is associated with susceptibility to Hirschsprung's disease in Chinese Han population. Pediatric research 2020 May . Yu Xian-Xian, Chu Xun, Wu Wen-Jie, Wei Zhi-Liang, Song Huan-Lei, Bai Mei-Rong, Lu Yan-Jiao, Gu Bei-Lin, Gong Yi-Ming, Cai W |
Excess of de novo variants in genes involved in chromatin remodelling in patients with marfanoid habitus and intellectual disability. Journal of medical genetics 2020 4 57 (7): 466-474. Chevarin Martin, Duffourd Yannis, A Barnard Rebecca, Moutton Sébastien, Lecoquierre François, Daoud Fatma, Kuentz Paul, Cabret Caroline, Thevenon Julien, Gautier Elodie, Callier Patrick, St-Onge Judith, Jouan Thibaud, Lacombe Didier, Delrue Marie Ange, Goizet Cyril, Morice-Picard Fanny, Van-Gils Julien, Munnich Arnold, Lyonnet Stanislas, Cormier-Daire Valérie, Baujat Geneviève, Holder Muriel, Petit Florence, Leheup Bruno, Odent Sylvie, Jouk Pierre-Simon, Lopez Gipsy, Geneviève David, Collignon Patrick, Martin-Coignard Dominique, Jacquette Aurélia, Perrin Laurence, Putoux Audrey, Sarrazin Elisabeth, Amarof Khadija, Missotte Isabelle, Coubes Christine, Jagadeesh Sujatha, Lapi Elisabetta, Demurger Florence, Goldenberg Alice, Doco-Fenzy Martine, Mignot Cyril, Héron Delphine, Jean-Marçais Nolwenn, Masurel Alice, El Chehadeh Salima, Marle Nathalie, Huet Frédéric, Binquet Christine, Collod-Beroud Gwenaëlle, Arnaud Pauline, Hanna Nadine, Boileau Catherine, Jondeau Guillaume, Olaso Robert, Lechner Doris, Poe Charlotte, Assoum Mirna, Carmignac Virginie, Duplomb Laurence, Tran Mau-Them Frédéric, Philippe Christophe, Vitobello Antonio, Bruel Ange-Line, Boland Anne, Deleuze Jean-François, Thauvin-Robinet Christel, Rivière Jean-Baptiste, O'Roak Brian J, Faivre Lauren |
Computational analyses on genetic alterations in the NSD genes family and the implications for colorectal cancer development. Ecancermedicalscience 2020 3 14 1001. D'Afonseca Vívian, Gónzalez Glória, Salazar Marcela, Arencibia Ariel |
The Association of Scoliosis and NSD1 Gene Deletion in Sotos Syndrome Patients. Spine 2020 12 46 (13): E726-E733. Machida Masafumi, Katoh Hiroyuki, Machida Masayoshi, Miyake Atsushi, Taira Katsuaki, Ohashi Hirofu |
Hyperleukocytosis predicts inferior clinical outcome in pediatric acute myeloid leukemia. Hematology (Amsterdam, Netherlands) 2020 Dec 25 (1): 507-514. Xu Lu-Hong, Wang Jing-Wen, Wang Yin, Yang Feng-Yi |
Integrative Analysis of miRNAs Identifies Clinically Relevant Epithelial and Stromal Subtypes of Head and Neck Squamous Cell Carcinoma. Clinical cancer research : an official journal of the American Association for Cancer Research 2020 11 27 (3): 831-842. Holt Jeremiah, Walter Vonn, Yin Xiaoying, Marron David, Wilkerson Matthew D, Choi Hyo Young, Zhao Xiaobei, Jo Heejoon, Hayes David Neil, Ko Yoon |
Subtyping of head and neck squamous cell cancers based on immune signatures. International immunopharmacology 2021 Jul 99 108007. Song Dandan, Lyu Haoyu, Feng Qiushi, Luo Jiangti, Li Lin, Wang Xiaoshe |
Establishment of a Plasticity-Associated Risk Model Based on a SOX2- and SOX9-Related Gene Set in Head and Neck Squamous Cell Carcinoma. Molecular cancer research : MCR 2021 7 19 (10): 1676-1687. Khorani Karam, Schwaerzler Julia, Burkart Sebastian, Kurth Ina, Holzinger Dana, Flechtenmacher Christa, Plinkert Peter K, Zaoui Karim, Hess Joch |
Genetic heterogeneity of disorders with overgrowth and intellectual disability: Experience from a center in North India. American journal of medical genetics. Part A 2021 5 185 (8): 2345-2355. Moirangthem Amita, Mandal Kausik, Saxena Deepti, Srivastava Priyanka, Gambhir Poonam Singh, Agrawal Neha, Shambhavi Arya, Nampoothiri Sheela, Phadke Shubha |
Low expression of NSD1, NSD2, and NSD3 define a subset of human papillomavirus-positive oral squamous carcinomas with unfavorable prognosis. Infectious agents and cancer 2021 Feb 16 (1): 13. Gameiro Steven F, Ghasemi Farhad, Zeng Peter Y F, Mundi Neil, Howlett Christopher J, Plantinga Paul, Barrett John W, Nichols Anthony C, Mymryk Joe |
Impact of KMT2A Rearrangement and CSPG4 Expression in Pediatric Acute Myeloid Leukemia. Cancers 2021 10 13 (19): . Hoffmeister Lina Marie, Orhan Eser, Walter Christiane, Niktoreh Naghmeh, Hanenberg Helmut, von Neuhoff Nils, Reinhardt Dirk, Schneider Mark |
Genetic Characteristics According to Subgroup of Acute Myeloid Leukemia with Myelodysplasia-Related Changes. Journal of clinical medicine 2022 5 11 (9): . Kang Dain, Jung Jin, Park Silvia, Cho Byung-Sik, Kim Hee-Je, Kim Yeojae, Lee Jong-Mi, Kim Hoon Seok, Ahn Ari, Kim Myungshin, Kim Yongg |
Potential Involvement of NSD1, KRT24 and ACACA in the Genetic Predisposition to Colorectal Cancer. Cancers 2022 2 14 (3): . Quintana Isabel, Mur Pilar, Terradas Mariona, García-Mulero Sandra, Aiza Gemma, Navarro Matilde, Piñol Virginia, Brunet Joan, Moreno Victor, Sanz-Pamplona Rebeca, Capellá Gabriel, Valle Lau |
UBTF-internal tandem duplication as a novel poor prognostic factor in pediatric acute myeloid leukemia. Genes, chromosomes & cancer 2022 11 62 (4): 202-209. Kaburagi Taeko, Shiba Norio, Yamato Genki, Yoshida Kenichi, Tabuchi Ken, Ohki Kentaro, Ishikita Etsuko, Hara Yusuke, Shiraishi Yuichi, Kawasaki Hirohide, Sotomatsu Manabu, Takizawa Takumi, Taki Tomohiko, Kiyokawa Nobutaka, Tomizawa Daisuke, Horibe Keizo, Miyano Satoru, Taga Takashi, Adachi Souichi, Ogawa Seishi, Hayashi Yasuhi |
Genome-Wide DNA Methylation Profiling Solves Uncertainty in Classifying NSD1 Variants. Genes 2022 11 13 (11): . Ferilli Marco, Ciolfi Andrea, Pedace Lucia, Niceta Marcello, Radio Francesca Clementina, Pizzi Simone, Miele Evelina, Cappelletti Camilla, Mancini Cecilia, Galluccio Tiziana, Andreani Marco, Iascone Maria, Chiriatti Luigi, Novelli Antonio, Micalizzi Alessia, Matraxia Marta, Menale Lucia, Faletra Flavio, Prontera Paolo, Pilotta Alba, Bedeschi Maria Francesca, Capolino Rossella, Baban Anwar, Seri Marco, Mammì Corrado, Zampino Giuseppe, Digilio Maria Cristina, Dallapiccola Bruno, Priolo Manuela, Tartaglia Mar |
Investigation of Copy Number Variation in South African Patients With Congenital Heart Defects. Circulation. Genomic and precision medicine 2022 Oct 101161CIRCGEN121003510. Saacks Nicole A, Eales James, Spracklen Timothy F, Aldersley Thomas, Human Paul, Verryn Mark, Lawrenson John, Cupido Blanche, Comitis George, De Decker Rik, Fourie Barend, Swanson Lenise, Joachim Alexia, Brooks Andre, Ramesar Raj, Shaboodien Gasnat, Keavney Bernard D, Zühlke Liesl |
Clinical exome sequencing uncovers a high frequency of Mendelian disorders in infants with stroke: A retrospective analysis. American journal of medical genetics. Part A 2022 Sep . Kumar Runjun D, Meng Linyan, Liu Pengfei, Miyake Christina Y, Worley Kim C, Bi Weimin, Lalani Seema |
Angioimmunoblastic T-cell lymphoma: Novel recurrent mutations and prognostic biomarkers by cell-free DNA profiling. British journal of haematology 2023 8 . Chunlan Zhang, Biqin Mou, Juan Xu, Jie Wang, Qinyu Liu, Yunfan Yang, Wenjiao Tang, Xushu Zhong, Caigang |
The epigenetic modifier lysine methyltransferase 2C is frequently mutated in gastric remnant carcinoma. The journal of pathology. Clinical research 2023 7 . Bo Sun, Haojie Chen, Jiawen Lao, Cong Tan, Yue Zhang, Zhen Shao, Dazhi |
Clinical implications of NUP98::NSD1 fusion at diagnosis in adult FLT3-ITD positive AML. European journal of haematology 2023 7 . Toru Miyajima, Masahiro Onozawa, Shota Yoshida, Naoki Miyashita, Hiroyuki Kimura, Shogo Takahashi, Shota Yokoyama, Toshihiro Matsukawa, Hideki Goto, Junichi Sugita, Shinichi Fujisawa, Daisuke Hidaka, Reiki Ogasawara, Akio Mori, Satomi Matsuoka, Akio Shigematsu, Kentaro Wakasa, Ikumi Kasahara, Tomoyuki Saga, Junichi Hashiguchi, Yukari Takeda, Makoto Ibata, Tsutsumi Yutaka, Katsuya Fujimoto, Takeshi Kondo, Takanori Teshi |
Cognitive, adaptive and behavioral profile in Sotos syndrome children with 5q35 microdeletion or intragenic variants. American journal of medical genetics. Part A 2023 4 . Siracusano Martina, Riccioni Assia, Frattale Ilaria, Arturi Lucrezia, Dante Caterina, Galasso Cinzia, Gialloreti Leonardo Emberti, Conteduca Giuseppina, Testa Barbara, Malacarne Michela, Coviello Domenico, Mazzone Lui |
An investigation of the etiology and follow-up findings in 35 children with overgrowth syndromes, including biallelic SUZ12 variant. American journal of medical genetics. Part A 2023 3 . Yüksel Ülker Aylin, Uluda? Alkaya Dilek, Ça?layan Ahmet Okay, Usluer Esra, Aykut Ayça, Aslanger Ayça, Vural Mehmet, Tüysüz Beyh |
Identification of tumor mutation burden-associated molecular and clinical features in cancer by analyzing multi-omics data. Frontiers in immunology 2023 3 14 1090838. Li Mengyuan, Gao Xuejiao, Wang Xiaoshe |
Comprehensive molecular and clinical characterization of NUP98 fusions in pediatric acute myeloid leukemia. Haematologica 2023 2 . Bertrums Eline J M, Smith Jenny L, Harmon Lauren, Ries Rhonda E, Wang Yi-Cheng J, Alonzo Todd A, Menssen Andrew J, Chisholm Karen M, Leonti Amanda R, Tarlock Katherine, Ostronoff Fabiana, Pogosova-Agadjanyan Era L, Kaspers Gertjan J L, Hasle Henrik, Dworzak Michael, Walter Christiane, Muhlegger Nora, Morerio Cristina, Pardo Laura, Hirsch Betsy, Raimondi Susana, Cooper Todd M, Aplenc Richard, Gamis Alan S, Kolb Edward A, Farrar Jason E, Stirewalt Derek, Ma Xiaotu, Shaw Tim I, Furlan Scott N, Brodersen Lisa Eidenschink, Loken Michael R, Van den Heuvel-Eibrink Marry M, Zwaan C Michel, Triche Timothy J, Goemans Bianca F, Meshinchi Sohe |
NSD1 Mutations and Pediatric High-Grade Gliomas: A Comparative Genomic Study in Primary and Recurrent Tumors. Diagnostics (Basel, Switzerland) 2023 1 13 (1): . d'Amati Antonio, Nicolussi Arianna, Miele Evelina, Mastronuzzi Angela, Rossi Sabrina, Gianno Francesca, Buttarelli Francesca Romana, Minasi Simone, Lodeserto Pietro, Gardiman Marina Paola, Viscardi Elisabetta, Coppa Anna, Donofrio Vittoria, Giovannoni Isabella, Giangaspero Felice, Antonelli Mani |
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- Page last updated:Apr 29, 2024
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