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1. Full Text Comprehensive Study of the Clinical Phenotype of Germline BAP1 Variant-Carrying Families Worldwide
by Walpole, Sebastian and Walpole, Sebastian and Pritchard, Antonia L and Pritchard, Antonia L and Cebulla, Colleen M and Pilarski, Robert and Stautberg, Meredith and Stautberg, Meredith and Davidorf, Frederick H and De La Fouchardière, Arnaud and de la Fouchardière, Arnaud and Cabaret, Odile and Cabaret, Odile and Golmard, Lisa and Golmard, Lisa and Stoppa-Lyonnet, Dominique and Stoppa-Lyonnet, Dominique and Garfield, Erin and Njauw, Ching-Ni and Cheung, Mitchell and Turunen, Joni A and Turunen, Joni A and Repo, Pauliina and Repo, Pauliina and Järvinen, Reetta-Stiina and Järvinen, Reetta-Stiina and van Doorn, Remco and Jager, Martine J and Luyten, Gregorius P.M and Luyten, Gregorius P M and Marinkovic, Marina and Chau, Cindy and Potrony, Miriam and Potrony, Miriam and Höiom, Veronica and Helgadottir, Hildur and Helgadottir, Hildur and Pastorino, Lorenza and Pastorino, Lorenza and Bruno, William and Bruno, William and Andreotti, Virginia and Andreotti, Virginia and Dalmasso, Bruna and Dalmasso, Bruna and Ciccarese, Giulia and Ciccarese, Giulia and Queirolo, Paola and Queirolo, Paola and Mastracci, Luca and Wadt, Karin and Kiilgaard, Jens Folke and Kiilgaard, Jens Folke and Speicher, Michael R and van Poppelen, Natasha and Kilic, Emine and Kilic, Emine and Al-Jamal, Rana T and Al-Jamal, Rana'a T and Dianzani, Irma and Dianzani, Irma and Betti, Marta and Betti, Marta and Bergmann, Carsten and Bergmann, Carsten and Santagata, Sandro and Dahiya, Sonika and Dahiya, Sonika and Taibjee, Saleem and Taibjee, Saleem and Burke, Jo and Burke, Jo and Poplawski, Nicola and Poplawski, Nicola and O'Shea, Sally J and O'Shea, Sally J and Newton-Bishop, Julia and Adlard, Julian and Adlard, Julian and Adams, David J and Adams, David J and Lane, Anne-Marie and Lane, Anne-Marie and Hayward, Nicholas K and Kim, Ivana and Klebe, Sonja and Abdel Rahman, Mohamed H and Racher, Hilary and Harbour, J William and Nickerson, Michael L and Murali, Rajmohan and Palmer, Jane M and Howlie, Madeleine and Symmons, Judith and Hamilton, Hayley and Warrier, Sunil and Glasson, William and Johansson, Peter and Robles-Espinoza, Carla Daniela and Ossio, Raul and ...
Journal of the National Cancer Institute, ISSN 0027-8874, 12/2018, Volume 110, Issue 12, pp. 1328 - 1341
Background: The BRCA1-associated protein-1 (BAP1) tumor predisposition syndrome (BAP1-TPDS) is a hereditary tumor syndrome caused by germline pathogenic... 
CHOLANGIOCARCINOMA | PROTEIN-1 | UVEAL MELANOMA | ONCOLOGY | DISEASE | MUTATIONS PREDISPOSE | TUMOR-SUPPRESSOR | MALIGNANT MESOTHELIOMA | RENAL-CELL CARCINOMA | HYDROLASE | PREDICTION
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2. Full Text A mouse model of schnyder corneal dystrophy with the N100S Point Mutation
by Dong, Fei and Jin, Xueting and Boettler, Michelle A and Sciulli, Harrison and Abu-Asab, Mones and Del Greco, Christina and Wang, Shurong and Hu, Yueh-Chiang and Campos, Maria M and Jackson, Shelley N and Muller, Ludovic and Woods, Amina S and Combs, Christian A and Zhang, Jianhua and Nickerson, Michael L and Kruth, Howard S and Weiss, Jayne S and Kao, Winston W
Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 10219 - 12
Schnyder corneal dystrophy (SCD) is a rare autosomal dominant disease in humans, characterized by abnormal deposition of cholesterol and phospholipids in... 
UNESTERIFIED CHOLESTEROL | DNA COPY NUMBER | MULTIDISCIPLINARY SCIENCES | MICE | GENERATION | UBIAD1 GENE | ACCUMULATION | MITOCHONDRIAL-DNA | TERE1 | DELETIONS | DAMAGE | CRISPR | Cornea | Phenotypes | Wound healing | Copy number | Heterozygotes | Mass spectroscopy | Confocal microscopy | Phospholipids | Mitochondrial DNA | Electron microscopy | Metabolism | Cholesterol | Endothelial cells | Homozygotes | Microscopy | Corneal dystrophy | Point mutation | Mutation | Dystrophy | Lipid metabolism | Genotypes
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3. Full Text The Cancer Genome Atlas Comprehensive Molecular Characterization of Renal Cell Carcinoma
by Ricketts, Christopher J and De Cubas, Aguirre A and Fan, Cheng and Fan, Huihui and Smith, Christof C and Smith, Jennifer and Lang, James and Lang, Martin and Reznik, Ed and Bowlby, Reanne and Gibb, Ewan A and Akbani, Rehan and Beroukhim, Rameen and Bottaro, Donald P and Choueiri, Toni K and Gibbs, Richard A and Godwin, Andrew K and Godwin, Eryn M and Haake, Scott and Hakimi, A. Ari and Henske, Elizabeth P and Hsieh, James J and Ho, Thai and Ho, Thai H and Kanchi, Rupa S and Krishnan, Bhavani and Kwiatkowski, David J and Lui, Wembin and Merino, Maria J and Mills, Gordon B and Myers, Jerome and Nickerson, Michael L and Reuter, Victor E and Reuter, Victor and Schmidt, Laura S and Schmidt, Heather K and Shelley, C. Simon and Shelley, Carl Simon and Shen, Hui and Shuch, Brian and Signoretti, Sabina and Srinivasan, Ramaprasad and Tamboli, Pheroze and Thomas, George and Vincent, Benjamin G and Vocke, Cathy D and Wheeler, David A and Yang, Lixing and Yang, Ian and Yang, Ju Dong and Yang, Hannah and Yang, Liming and Kim, Jaegil and Kim, William Y and Robertson, A. Gordon and Caesar-Johnson, Samantha J and Demchok, John A and Felau, Ina and Kasapi, Melpomeni and Ferguson, Martin L and Hutter, Carolyn M and Sofia, Heidi J and Tarnuzzer, Roy and Wang, Timothy and Wang, Linghua and Wang, Jioajiao and Wang, Min and Wang, Zhining and Wang, Jing and Zenklusen, Jean C and Zhang, Hailei and Zhang, Jiashan (Julia) and Zhang, Wei and Zhang, Hongxin and Zhang, Lizhi and Zhang, Jiexin and Zhang, Hongzheng and Chudamani, Sudha and Liu, Wenbin and Liu, Jia and Liu, Yuexin and Liu, Xiuping and Lolla, Laxmi and Naresh, Rashi and Pihl, Todd and Sun, Qiang and Sun, Yichao and Wan, Yunhu and Wu, Ye and Cho, Juok and DeFreitas, Timothy and Frazer, Scott and Gehlenborg, Nils and Getz, Gad and Heiman, David I and Lawrence, Michael S and Lin, Pei and Meier, Sam and Noble, Michael S and Saksena, Gordon and ... and Canc Genome Atlas Res Network and Cancer Genome Atlas Research Network
Cell Reports, ISSN 2211-1247, 04/2018, Volume 23, Issue 1, pp. 313 - 326.e5
Renal cell carcinoma (RCC) is not a single disease, but several histologically defined cancers with different genetic drivers, clinical courses, and... 
clear cell renal cell carcinoma | papillary renal cell carcinoma | chromophobe renal cell carcinoma | CDKN2A | PanCanAtlas | immune signature | chromatin remodeling | DNA hypermethylation | TCGA | GENETIC-BASIS | MESSENGER-RNA | RNA-SEQ | LANDSCAPE | SOMATIC POINT MUTATIONS | SEQUENCING DATA | CLASS DISCOVERY | EXPRESSION | KIDNEY CANCER | BREAST | CELL BIOLOGY | Index Medicus
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4. Full Text Abstract 2379: Nuclear lemur tyrosine kinase-2 regulates RNA polymerase II dependent transcription in prostate cancer
by Shah, Kalpit and Foley, Justin and Nickerson, Michael L and Dean, Michael and Bradbury, Neil
Cancer Research, ISSN 0008-5472, 07/2017, Volume 77, Issue 13 Supplement, pp. 2379 - 2379
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5. Full Text Differences in Tumor VHL Mutation and Hypoxia-inducible Factor 2α Expression Between African American and White Patients with Clear Cell Renal Cell Carcinoma
by Callahan, Catherine L and Moore, Lee and Lenz, Petra and Linehan, W. Marston and Nickerson, Michael L and Rothman, Nathaniel and Purdue, Mark P
European Urology, ISSN 0302-2838, 05/2019, Volume 75, Issue 5, pp. 882 - 884
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6. Full Text Abstract 3352: Genome-wide enhancer identify signature predictive of metastatic phenotypes in bladder cancers
by Kim, Sohyoung and Varticovski, Lyuba and Lao, Qizong and Baek, Songjoon and Nickerson, Michael L and Sung, Myong-Hee and Grontved, Lars and Bethtrice, Thompson and Theodorescu, Dan and Agarwal, Piyush K and Dean, Michael and Hager, Gordon
Cancer Research, ISSN 0008-5472, 07/2017, Volume 77, Issue 13 Supplement, pp. 3352 - 3352
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7. Full Text Driver genes exome sequencing reveals distinct variants in African Americans with colorectal neoplasia
by Ashktorab, Hassan and Azimi, Hamed and Varma, Sudhir and Lee, Edward L and Laiyemo, Adeyinka O and Nickerson, Michael L and Brim, Hassan
Oncotarget, ISSN 1949-2553, 04/2019, Volume 10, Issue 27, pp. 2607 - 2624
Colorectal cancer (CRC) is the third leading cause of cancer-related deaths in the United States. African Americans are disproportionately affected by CRC. Our... 
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8. Full Text Mo2074 - Distinctive DNA Mismatch Repair and APC Variants in African American with Colorectal Neoplasia
by Ashktorab, Hassan and Varma, Sudhir and Azimi, Hamed and Nickerson, Michael L and Brim, Hassan
Gastroenterology, ISSN 0016-5085, 04/2017, Volume 152, Issue 5, pp. S842 - S842
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9. Full Text "Mandibulofacial dysostosis with microcephaly" caused by EFTUD2 mutations: Expanding the phenotype
by Luquetti, Daniela V and Hing, Anne V and Rieder, Mark J and Nickerson, Deborah A and Turner, Emily H and Smith, Joshua and Park, Sarah and Cunningham, Michael L
American Journal of Medical Genetics, Part A, ISSN 1552-4825, 01/2013, Volume 161, Issue 1, pp. 108 - 113
Heterozygous mutations in the EFTUD2 were identified in 12 individuals with a rare sporadic craniofacial condition termed Mandibulofacial dysostosis with... 
EFTUD2 | Craniofacial development | Oculo-auriculo-vertebral spectrum (OAVS) | Epibulbar dermoid | Craniofacial microsomia | Mandibulofacial dysostosis | Choanal atresia | choanal atresia | COMPLEX | mandibulofacial dysostosis | craniofacial development | craniofacial microsomia | epibulbar dermoid | oculo-auriculo-vertebral spectrum (OAVS) | GENETICS & HEREDITY | TREACHER-COLLINS-SYNDROME | HAPLOINSUFFICIENCY | Microcephaly - genetics | Humans | Child, Preschool | Microcephaly - diagnosis | Infant | Male | DNA-Binding Proteins - genetics | DNA-Binding Proteins - metabolism | Exome | DNA Helicases - metabolism | Mandibulofacial Dysostosis - genetics | Phenotype | Image Processing, Computer-Assisted | Mandibulofacial Dysostosis - diagnosis | DNA Mutational Analysis | Peptide Elongation Factor Tu - genetics | CHARGE Syndrome - genetics | Mutation | Genomics - methods | DNA Helicases - genetics | Cohort Studies | Index Medicus | CHARGE syndrome
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10. Full Text Abstract 355: TET2-loss modifies androgen signaling in prostate cancer
by Nickerson, Michael L and Das, Sudipto and Im, Kate and Turan, Sevilay and Berndt, Sonja and Li, Hongchuan and Lou, Hong and Brodie, Seth and Shah, Kalpit and Billaud, Jean-Noel and Zhang, Tongwu and Boland, Joseph and Anderson, Stephen and Yeager, Meredith and Dean, Michael and Andresson, Thorkell
Cancer Research, ISSN 0008-5472, 07/2017, Volume 77, Issue 13 Supplement, pp. 355 - 355
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11. Full Text Abstract 4237: Differences in the frequencies of tumorVHLmutation and HIF-2α expression between black and white patients with clear cell renal carcinoma
by Callahan, Catherine L and Moore, Lee E and Lenz, Petra and Schwartz, Kendra and Ruterbusch, Julie and Davis, Faith and Chow, Wong-Ho and Linehan, W. Marston and Merino, Maria J and Hewitt, Stephen M and Rothman, Nathaniel and Hofmann, Jonathan N and Nickerson, Michael L and Purdue, Mark P
Cancer Research, ISSN 0008-5472, 07/2018, Volume 78, Issue 13 Supplement, pp. 4237 - 4237
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12. Full Text Abstract 1105: Clinical associations between altered bladder cancer genes
by Nickerson, Michael L and Im, Kate M and Turan, Sevilay and Moore, Lee E and Dean, Michael and Theodorescu, Dan
Cancer Research, ISSN 0008-5472, 08/2015, Volume 75, Issue 15 Supplement, pp. 1105 - 1105
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13. Full Text Adolescent Hippocampal and Prefrontal Brain Activation During Performance of the Virtual Morris Water Task
by Sneider, Jennifer T and Cohen-Gilbert, Julia E and Hamilton, Derek A and Stein, Elena R and Golan, Noa and Oot, Emily N and Seraikas, Anna M and Rohan, Michael L and Harris, Sion K and Nickerson, Lisa D and Silveri, Marisa M
Frontiers in Human Neuroscience, ISSN 1662-5161, 06/2018, Volume 12, pp. 238 - 238
The frontal cortex undergoes substantial structural and functional changes during adolescence and significant developmental changes also occur in the... 
Morris water task | Adolescence | Prefrontal cortex | BOLD fMRI | Hippocampus | Spatial memory | YOUNG-ADULTS | hippocampus | spatial memory | prefrontal cortex | COGNITIVE-DEVELOPMENT | NEUROSCIENCES | RETRIEVAL | PSYCHOLOGY | CORTEX | BOLD RESPONSE | adolescence | SEX-DIFFERENCES | NAVIGATION | MAZE | WORKING-MEMORY | Psychological aspects | Brain | Usage | Magnetic resonance imaging | Analysis | Health aspects | Psychophysiology | Neuroimaging | Executive function | Nuclear magnetic resonance--NMR | Laboratories | Neurobiology | Mental task performance | Alcohol | Cortex (motor) | Motor task performance | Males | Child development | Developmental stages | Cortex (frontal) | Functional magnetic resonance imaging | Teenagers | Drug use | Cortex (prefrontal) | Medical imaging | Animal memory | Brain mapping | Sex differences | Gender differences | Latency | Studies | Animal behavior | Adults | Short term memory | Structure-function relationships
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14. Full Text Abstract 474: Changes in global chromatin landscape identify bladder cancer progression
by Kim, Sohyoung and Varticovski, Lyuba and Grontved, Lars and Baek, Songjoon and Thompson, Bethrice and Dean, Michael and Theodoresco, Daniel and Nickerson, Michael L and Hager, Gordon L
Cancer Research, ISSN 0008-5472, 10/2014, Volume 74, Issue 19 Supplement, pp. 474 - 474
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15. Full Text Abstract 4782: Genome-wide chromatin profiling in bladder and prostate cancers
by Kim, Sohyoung and Varticovski, Lyuba and Lao, Qizong and Baek, Songjoon and Sung, Myong-Hee and Grøntved, Lars and Nickerson, Michael L and Thompson, Bethtrice and Theodorescu, Dan and Dean, Michael and Hager, Gordon H
Cancer Research, ISSN 0008-5472, 08/2015, Volume 75, Issue 15 Supplement, pp. 4782 - 4782
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16. Full Text Abstract 454:TET2alterations facilitate progression of metastatic prostate cancer
by Nickerson, Michael L and Das, Sudipto and Lou, Hong and Li, Hongchuan and Turan, Sevilay and Im, Kate and Anderson, Stephen and Andresson, Thorkell and Dean, Michael
Cancer Research, ISSN 0008-5472, 10/2014, Volume 74, Issue 19 Supplement, pp. 454 - 454
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17. Full Text Sa1942 Targeted Cancer Gene Sequencing Identifies Potential Causative Novel Candidate Mutations in African Americans Colon Carcinogenesis
by Ashktorab, Hassan and Nickerson, Michael L and Lee, Edward L and Shokrani, Babk and Afsari, Ali and Laiyemo, Adeyinka O and Varma, Sudhir and Bass, Sara E and Boland, Joseph and Huang, Wen-Yi and Yeager, Meredith and Moore, Lee E and Haidary, Tahmineh and Brim, Hassan
Gastroenterology, ISSN 0016-5085, 2015, Volume 148, Issue 4, pp. S-362 - S-362
Gastroenterology and Hepatology | African Americans | Genetic aspects | Colon cancer | Cancer
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18. Full Text Whole-genome and whole-exome sequencing of bladder cancer identifies frequent alterations in genes involved in sister chromatid cohesion and segregation
by Guo, Guangwu and Sun, Xiaojuan and Chen, Chao and Wu, Song and Huang, Peide and Li, Zesong and Dean, Michael and Huang, Yi and Jia, Wenlong and Zhou, Quan and Tang, Aifa and Yang, Zuoquan and Li, Xianxin and Song, Pengfei and Zhao, Xiaokun and Ye, Rui and Zhang, Shiqiang and Lin, Zhao and Qi, Mingfu and Wan, Shengqing and Xie, Liangfu and Fan, Fan and Nickerson, Michael L and Zou, Xiangjun and Hu, Xueda and Xing, Li and Lv, Zhaojie and Mei, Hongbin and Gao, Shengjie and Liang, Chaozhao and Gao, Zhibo and Lu, Jingxiao and Yu, Yuan and Liu, Chunxiao and Li, Lin and Fang, Xiaodong and Jiang, Zhimao and Yang, Jie and Li, Cailing and Zhao, Xin and Chen, Jing and Zhang, Fang and Lai, Yongqi and Lin, Zheguang and Zhou, Fangjian and Chen, Hao and Chan, Hsiao Chang and Tsang, Shirley and Theodorescu, Dan and Li, Yingrui and Zhang, Xiuqing and Wang, Jian and Yang, Huanming and Gui, Yaoting and Wang, Jun and Cai, Zhiming
Nature Genetics, ISSN 1061-4036, 12/2013, Volume 45, Issue 12, pp. 1459 - 1463
Bladder cancer is one of the most common cancers worldwide, with transitional cell carcinoma (TCC) being the predominant form. Here we report a genomic... 
ANEUPLOIDY | GENETICS & HEREDITY | MUTATIONS | FUSIONS | FGFR3 | CARCINOMA | VARIANT | Sister Chromatid Exchange - genetics | Genome-Wide Association Study | Gene Frequency | Humans | Sequence Analysis, DNA | Case-Control Studies | Exome - genetics | Urinary Bladder Neoplasms - genetics | Cell Transformation, Neoplastic - genetics | Base Sequence | Polymorphism, Single Nucleotide | Carcinoma, Transitional Cell - genetics | Chromosome Segregation - genetics | Genetic aspects | Research | Gene mutations | Bladder cancer | Identification and classification | Cancer | Survival analysis | Genes | Medical prognosis | Cell division | Genomes | Tumorigenesis | Mutation | Tumors | Index Medicus
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