Human Genome Epidemiology Literature Finder
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Records 1 - 23 (of 23 Records) |
| Query Trace: Disease and ARID1B[original query] |
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APOE and BCHE as modulators of cerebral amyloid deposition: a florbetapir PET genome-wide association study.
Molecular psychiatry 2014 Mar 19 (3): 351-7. Ramanan V K, Risacher S L, Nho K, Kim S, Swaminathan S, Shen L, Foroud T M, Hakonarson H, Huentelman M J, Aisen P S, Petersen R C, Green R C, Jack C R, Koeppe R A, Jagust W J, Weiner M W, Saykin A J, |
| Identification of new genetic susceptibility loci for breast cancer through consideration of gene-environment interactions. Genetic epidemiology 2014 Jan 38 (1): 84-93. Schoeps Anja, Rudolph Anja, Seibold Petra, Dunning Alison M, Milne Roger L, Bojesen Stig E, Swerdlow Anthony, Andrulis Irene, Brenner Hermann, Behrens Sabine, Orr Nicholas, Jones Michael, Ashworth Alan, Li Jingmei, Cramp Helen, Connley Dan, Czene Kamila, Darabi Hatef, Chanock Stephen J, Lissowska Jolanta, Figueroa Jonine D, Knight Julia, Glendon Gord, Mulligan Anna M, Dumont Martine, Severi Gianluca, Baglietto Laura, Olson Janet, Vachon Celine, Purrington Kristen, Moisse Matthieu, Neven Patrick, Wildiers Hans, Spurdle Amanda, Kosma Veli-Matti, Kataja Vesa, Hartikainen Jaana M, Hamann Ute, Ko Yon-Dschun, Dieffenbach Aida K, Arndt Volker, Stegmaier Christa, Malats Núria, Arias Perez José I, Benítez Javier, Flyger Henrik, Nordestgaard Børge G, Truong Thérèse, Cordina-Duverger Emilie, Menegaux Florence, dos Santos Silva Isabel, Fletcher Olivia, Johnson Nichola, Häberle Lothar, Beckmann Matthias W, Ekici Arif B, Braaf Linde, Atsma Femke, van den Broek Alexandra J, Makalic Enes, Schmidt Daniel F, Southey Melissa C, Cox Angela, Simard Jacques, Giles Graham G, Lambrechts Diether, Mannermaa Arto, Brauch Hiltrud, Guénel Pascal, Peto Julian, Fasching Peter A, Hopper John, Flesch-Janys Dieter, Couch Fergus, Chenevix-Trench Georgia, Pharoah Paul D P, Garcia-Closas Montserrat, Schmidt Marjanka K, Hall Per, Easton Douglas F, Chang-Claude Jen |
| Genetic variants associated with vein graft stenosis after coronary artery bypass grafting.
The heart surgery forum 2015 18 (1): E1-5. Shah Asad A, Haynes Carol, Craig Damian M, Sebek Jacqueline, Grass Elizabeth, Abramson Karen, Hauser Elizabeth, Gregory Simon G, Kraus William E, Smith Peter K, Shah Svati |
| Analysis of Paired Primary-Metastatic Hormone-Receptor Positive Breast Tumors (HRPBC) Uncovers Potential Novel Drivers of Hormonal Resistance. PloS one 2016 11 (5): e0155840. Manso Luis, Mourón Silvana, Tress Michael, Gómez-López Gonzalo, Morente Manuel, Ciruelos Eva, Rubio-Camarillo Miriam, Rodriguez-Peralto Jose Luis, Pujana Miguel A, Pisano David G, Quintela-Fandino Migu |
| Analysis of functional germline variants in APOBEC3 and driver genes on breast cancer risk in Moroccan study population. BMC cancer 2016 16 (1): 165. Marouf Chaymaa, Göhler Stella, Filho Miguel Inacio Da Silva, Hajji Omar, Hemminki Kari, Nadifi Sellama, Försti As |
| ARID1B alterations identify aggressive tumors in neuroblastoma. Oncotarget 2017 Jul 8 (28): 45943-45950. Lee Soo Hyun, Kim Jung-Sun, Zheng Siyuan, Huse Jason T, Bae Joon Seol, Lee Ji Won, Yoo Keon Hee, Koo Hong Hoe, Kyung Sungkyu, Park Woong-Yang, Sung Ki |
| 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 |
| Novel caries loci in children and adults implicated by genome-wide analysis of families. BMC oral health 2018 6 18 (1): 98. Govil Manika, Mukhopadhyay Nandita, Weeks Daniel E, Feingold Eleanor, Shaffer John R, Levy Steven M, Vieira Alexandre R, Slayton Rebecca L, McNeil Daniel W, Weyant Robert J, Crout Richard J, Marazita Mary |
| Rare Copy Number Variations and Predictors in Children With Intellectual Disability and Epilepsy. Frontiers in neurology 2018 12 9 947. Kessi Miriam, Xiong Juan, Wu Liwen, Yang Lifen, He Fang, Chen Chen, Pang Nan, Duan Haolin, Zhang Wen, Arafat Ahmed, Yin Fei, Peng Ji |
| Targeted next generation sequencing in 112 Chinese patients with intellectual disability/developmental delay: novel mutations and candidate gene. BMC medical genetics 2019 5 20 (1): 80. Yan Huifang, Shi Zhen, Wu Ye, Xiao Jiangxi, Gu Qiang, Yang Yanling, Li Ming, Gao Kai, Chen Yinyin, Yang Xiaoping, Ji Haoran, Cao Binbin, Duan Ruoyu, Jiang Yuwu, Wang Jingm |
| Coffin-Siris Syndrome-1: Report of five cases from Asian populations with truncating mutations in the ARID1B gene. Journal of the neurological sciences 2020 4 414 116819. Lian Sophie, Ting Teck Wah, Lai Angeline H M, Tan Ee-Shien, Wei Heming, Cham Breana, Tan Ene-Ch |
| Mammalian SWI/SNF Complex Genomic Alterations and Immune Checkpoint Blockade in Solid Tumors. Cancer immunology research 2020 4 8 (8): 1075-1084. Abou Alaiwi Sarah, Nassar Amin H, Xie Wanling, Bakouny Ziad, Berchuck Jacob E, Braun David A, Baca Sylvan C, Nuzzo Pier Vitale, Flippot Ronan, Mouhieddine Tarek H, Spurr Liam F, Li Yvonne Y, Li Taiwen, Flaifel Abdallah, Steinharter John A, Margolis Claire A, Vokes Natalie I, Du Heng, Shukla Sachet A, Cherniack Andrew D, Sonpavde Guru, Haddad Robert I, Awad Mark M, Giannakis Marios, Hodi F Stephen, Liu X Shirley, Signoretti Sabina, Kadoch Cigall, Freedman Matthew L, Kwiatkowski David J, Van Allen Eliezer M, Choueiri Toni |
| Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease. PLoS genetics 2021 Jul 17 (7): e1009679. Audain Enrique, Wilsdon Anna, Breckpot Jeroen, Izarzugaza Jose M G, Fitzgerald Tomas W, Kahlert Anne-Karin, Sifrim Alejandro, Wünnemann Florian, Perez-Riverol Yasset, Abdul-Khaliq Hashim, Bak Mads, Bassett Anne S, Benson D Woodrow, Berger Felix, Daehnert Ingo, Devriendt Koenraad, Dittrich Sven, Daubeney Piers Ef, Garg Vidu, Hackmann Karl, Hoff Kirstin, Hofmann Philipp, Dombrowsky Gregor, Pickardt Thomas, Bauer Ulrike, Keavney Bernard D, Klaassen Sabine, Kramer Hans-Heiner, Marshall Christian R, Milewicz Dianna M, Lemaire Scott, Coselli Joseph S, Mitchell Michael E, Tomita-Mitchell Aoy, Prakash Siddharth K, Stamm Karl, Stewart Alexandre F R, Silversides Candice K, Siebert Reiner, Stiller Brigitte, Rosenfeld Jill A, Vater Inga, Postma Alex V, Caliebe Almuth, Brook J David, Andelfinger Gregor, Hurles Matthew E, Thienpont Bernard, Larsen Lars Allan, Hitz Marc-Phill |
| SMARCA4 and Other SWItch/Sucrose NonFermentable Family Genomic Alterations in NSCLC: Clinicopathologic Characteristics and Outcomes to Immune Checkpoint Inhibition. Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer 2021 Apr . Alessi Joao V, Ricciuti Biagio, Spurr Liam F, Gupta Hersh, Li Yvonne Y, Glass Carolyn, Nishino Mizuki, Cherniack Andrew D, Lindsay James, Sharma Bijaya, Felt Kristen D, Rodig Scott J, Cheng Michael L, Sholl Lynette M, Awad Mark |
| Phenotypic and molecular spectra of patients with switch/sucrose nonfermenting complex-related intellectual disability disorders in Korea. BMC medical genomics 2021 10 14 (1): 254. Lee Yena, Choi Yunha, Seo Go Hun, Kim Gu-Hwan, Keum Changwon, Kim Yoo-Mi, Do Hyo-Sang, Choi Jeongmin, Choi In Hee, Yoo Han-Wook, Lee Beom H |
| An additional whole-exome sequencing study in 102 panel-undiagnosed patients: A retrospective study in a Chinese craniosynostosis cohort. Frontiers in genetics 2022 13 967688. Chen Jieyi, Zhang Ping, Peng Meifang, Liu Bo, Wang Xiao, Du Siyuan, Lu Yao, Mu Xiongzheng, Lu Yulan, Wang Sijia, Wu Yingz |
| Identification of distinct genomic features reveals frequent somatic AHNAK and PTEN mutations predominantly in primary malignant melanoma presenting in the ureter. Japanese journal of clinical oncology 2022 5 52 (8): 930-943. Huang Yan, Wei Lai, Huang Yuanbin, Wen Shuang, Liu Tianqing, Duan Xu, Wang Yutong, Zhang Hongshuo, Fan Bo, Hu B |
| DNA Copy Number Alterations and Copy Neutral Loss of Heterozygosity in Adult Ph-Negative Acute B-Lymphoblastic Leukemia: Focus on the Genes Involved. International journal of molecular sciences 2023 12 24 (24): . Natalya Risinskaya, Maria Gladysheva, Abdulpatakh Abdulpatakhov, Yulia Chabaeva, Valeriya Surimova, Olga Aleshina, Anna Yushkova, Olga Dubova, Nikolay Kapranov, Irina Galtseva, Sergey Kulikov, Tatiana Obukhova, Andrey Sudarikov, Elena Parovichniko |
| Genetic variants in African-American and Hispanic patients with breast cancer. Oncology letters 2023 1 25 (2): 51. Dutta Pranabananda, Keung Man Y, Wu Yanyuan, Vadgama Jaydutt |
| Admixture Mapping of Chronic Kidney Disease and Risk Factors in Hispanic/Latino Individuals From Central America Country of Origin. Circulation. Genomic and precision medicine 2024 7 e004314. Andrea R V R Horimoto, Quan Sun, James P Lash, Martha L Daviglus, Jianwen Cai, Karin Haack, Shelley A Cole, Timothy A Thornton, Sharon R Browning, Nora Franceschi |
| Unraveling the genetic architecture of blood unfolded p-53 among non-demented elderlies: novel candidate genes for early Alzheimer's disease. BMC genomics 2024 5 25 (1): 440. Arash Yaghoobi, Seyed Amir Malekpo |
| ARID1B-related disorder in 87 adults: Natural history and self-sustainability. Genetics in medicine open 2024 12 2 101873. P J van der Sluijs, M Gösgens, A J M Dingemans, P Striano, A Riva, C Mignot, A Faudet, G Vasileiou, M Walther, S A Schrier Vergano, M Alders, F S Alkuraya, I Alorainy, H S Alsaif, B Anderlid, I Bache, I van Beek, M Blanluet, B W van Bon, T Brunet, H Brunner, M L Carriero, P Charles, N Chatron, E Coccia, C Dubourg, R K Earl, E E Eichler, L Faivre, N Foulds, C Graziano, A M Guerrot, M O Hashem, S Heide, D Heron, S E Hickey, S M J Hopman, A Kattentidt-Mouravieva, J Kerkhof, J S Klein Wassink-Ruiter, E C Kurtz-Nelson, K Kušíková, M Kvarnung, F Lecoquierre, G S Leszinski, L Loberti, P L Magoulas, F Mari, I Maystadt, G Merla, J M Milunsky, S Moortgat, G Nicolas, M O ' Leary, S Odent, J R Ozmore, K Parbhoo, R Pfundt, M Piccione, A M Pinto, B Popp, A Putoux, H L Rehm, A Reis, A Renieri, J A Rosenfeld, M Rossi, E Salzano, P Saugier-Veber, M Seri, G Severi, F M Sonmez, G Strobl-Wildemann, K E Stuurman, E Uctepe, H Van Esch, G Vitetta, B B A de Vries, D Wahl, T Wang, P Zacher, K R Heitink, F G Ropers, D Steenbeek, T Rybak, G W E Sant |
| Clinical utility of plasma cell-free DNA in pancreatic neuroendocrine neoplasms. Endocrine-related cancer 2024 1 . Darren Cowzer, Ronak H Shah, Joanne F Chou, Ritika Kundra, Sippy Punn, Laura Fiedler, April DeMore, Marinela Capanu, Michael F Berger, Diane Reidy-Lagunes, Nitya R |
- Page last reviewed:Feb 1, 2024
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