1. 5-Hydroxymethylcytosine discriminates between parathyroid adenoma and carcinoma. Issue 1 (December 2016) Authors: Barazeghi, Elham; Gill, Anthony; Sidhu, Stan; Norlén, Olov; Dina, Roberto; Palazzo, F.; Hellman, Per; Stålberg, Peter; Westin, Gunnar Journal: Clinical epigenetics Issue: Volume 8:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A clinical-molecular update on azanucleoside-based therapy for the treatment of hematologic cancers. Issue 1 (December 2016) Authors: Diesch, Jeannine; Zwick, Anabel; Garz, Anne-Kathrin; Palau, Anna; Buschbeck, Marcus; Götze, Katharina Journal: Clinical epigenetics Issue: Volume 8:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A community effort to protect genomic data sharing, collaboration and outsourcing. (December 2017) Authors: Wang, Shuang; Jiang, Xiaoqian; Tang, Haixu; Wang, Xiaofeng; Bu, Diyue; Carey, Knox; Dyke, Stephanie; Fox, Dov; Jiang, Chao; Lauter, Kristin; Malin, Bradley; Sofia, Heidi; Telenti, Amalio; Wang, Lei; Wang, Wenhao; Ohno-Machado, Lucila Journal: Npj genomic medicine Issue: Volume 2(2017) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. A comparative study of k-spectrum-based error correction methods for next-generation sequencing data analysis. (July 2016) Authors: Akogwu, Isaac; Wang, Nan; Zhang, Chaoyang; Gong, Ping Journal: Human genomics Issue: Volume 10(2016)Supplement 2 Page Start: 49 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. A first-line diagnostic assay for limb-girdle muscular dystrophy and other myopathies. Issue 1 (December 2016) Authors: Monies, Dorota; Alhindi, Hindi; Almuhaizea, Mohamed; Abouelhoda, Mohamed; Alazami, Anas; Goljan, Ewa; Alyounes, Banan; Jaroudi, Dyala; AlIssa, Abdulelah; Alabdulrahman, Khalid; Subhani, Shazia; El-Kalioby, Mohamed; Faquih, Tariq; Wakil, Salma; Altassan, Nada; Meyer, Brian; Bohlega, Saeed Journal: Human genomics Issue: Volume 10:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. A gene expression signature identifying transient DNMT1 depletion as a causal factor of cancer-germline gene activation in melanoma. Issue 1 (December 2015) Authors: Cannuyer, Julie; Van Tongelen, Aurélie; Loriot, Axelle; De Smet, Charles Journal: Clinical epigenetics Issue: Volume 7:Issue 1(2015) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. A genomic case study of desmoplastic small round cell tumor: comprehensive analysis reveals insights into potential therapeutic targets and development of a monitoring tool for a rare and aggressive disease. Issue 1 (December 2016) Authors: Ferreira, Elisa; Barros, Bruna; de Souza, Jorge; Almeida, Renan; Torrezan, Giovana; Garcia, Sheila; Krepischi, Ana; Mello, Celso; Cunha, Isabela; Pinto, Clóvis; Soares, Fernando; Dias-Neto, Emmanuel; Lopes, Ademar; de Souza, Sandro; Carraro, Dirce Journal: Human genomics Issue: Volume 10:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. A methylation PCR method determines FMR1 activation ratios and differentiates premutation allele mosaicism in carrier siblings. Issue 1 (December 2016) Authors: Hadd, Andrew; Filipovic-Sadic, Stela; Zhou, Lili; Williams, Arianna; Latham, Gary; Berry-Kravis, Elizabeth; Hall, Deborah Journal: Clinical epigenetics Issue: Volume 8:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver–Russell and Beckwith–Wiedemann syndromes. Issue 1 (December 2016) Authors: Russo, Silvia; Calzari, Luciano; Mussa, Alessandro; Mainini, Ester; Cassina, Matteo; Di Candia, Stefania; Clementi, Maurizio; Guzzetti, Sara; Tabano, Silvia; Miozzo, Monica; Sirchia, Silvia; Finelli, Palma; Prontera, Paolo; Maitz, Silvia; Sorge, Giovanni; Calcagno, Annalisa; Maghnie, Mohamad; Div... Journal: Clinical epigenetics Issue: Volume 8:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver–Russell and Beckwith–Wiedemann syndromes. Issue 1 (December 2016) Authors: Russo, Silvia; Calzari, Luciano; Mussa, Alessandro; Mainini, Ester; Cassina, Matteo; Di Candia, Stefania; Clementi, Maurizio; Guzzetti, Sara; Tabano, Silvia; Miozzo, Monica; Sirchia, Silvia; Finelli, Palma; Prontera, Paolo; Maitz, Silvia; Sorge, Giovanni; Calcagno, Annalisa; Maghnie, Mohamad; Div... Journal: Clinical epigenetics Issue: Volume 8:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗