Index by Author

February 2014; 24 (2)
  1. A
  2. B
  3. C
  4. D
  5. E
  6. F
  7. G
  8. H
  9. I
  10. J
  11. K
  12. L
  13. M
  14. N
  15. O
  16. P
  17. Q
  18. R
  19. S
  20. T
  21. U
  22. V
  23. W
  24. X
  25. Y
  26. Z

A

  1. Abdel-Salam, Ghada

  2. Akagi, Keiko

  3. Al-Hassnan, Zuhair N.

  4. Alkuraya, Fowzan S.

  5. Alomar, Rana

  6. Al-Shidi, Tarfa

  7. Ansari, Shinu

  8. Antonarakis, Stylianos E.

    • Simultaneous identification and prioritization of variants in familial, de novo, and somatic genetic disorders with VariantMaster Genome Res. February 2014 24: 349-355; Published in Advance January 3, 2014, doi:10.1101/gr.163832.113

  9. Antoshechkin, Igor

  10. Aryee, Emmanuel

    • Systematic mapping of occluded genes by cell fusion reveals prevalence and stability of cis-mediated silencing in somatic cells Genome Res. February 2014 24: 267-280; Published in Advance December 5, 2013, doi:10.1101/gr.143891.112

  11. Avey, Denis

  12. Aymerich, Marta

    • Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia Genome Res. February 2014 24: 212-226; Published in Advance November 21, 2013, doi:10.1101/gr.152132.112
      OPEN ACCESS ARTICLE

B

  1. Bafna, Vineet

  2. Baker, Samuel W.

    • Systematic mapping of occluded genes by cell fusion reveals prevalence and stability of cis-mediated silencing in somatic cells Genome Res. February 2014 24: 267-280; Published in Advance December 5, 2013, doi:10.1101/gr.143891.112

  3. Bauer, Sebastian

    • Improved exome prioritization of disease genes through cross-species phenotype comparison Genome Res. February 2014 24: 340-348; Published in Advance October 25, 2013, doi:10.1101/gr.160325.113
      OPEN ACCESS ARTICLE

  4. Blanc, Julie

    • Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia Genome Res. February 2014 24: 212-226; Published in Advance November 21, 2013, doi:10.1101/gr.152132.112
      OPEN ACCESS ARTICLE

  5. Borowsky, Mark L.

  6. Bottani, Armand

    • Simultaneous identification and prioritization of variants in familial, de novo, and somatic genetic disorders with VariantMaster Genome Res. February 2014 24: 349-355; Published in Advance January 3, 2014, doi:10.1101/gr.163832.113

  7. Brannon, A. Rose

    • Variation in chromatin accessibility in human kidney cancer links H3K36 methyltransferase loss with widespread RNA processing defects Genome Res. February 2014 24: 241-250; Published in Advance October 24, 2013, doi:10.1101/gr.158253.113

  8. Bronner, Marianne E.

  9. Broutian, Tatevik R.

  10. Bugarija, Branimir

    • Systematic mapping of occluded genes by cell fusion reveals prevalence and stability of cis-mediated silencing in somatic cells Genome Res. February 2014 24: 267-280; Published in Advance December 5, 2013, doi:10.1101/gr.143891.112

C

  1. Campo, Elías

    • Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia Genome Res. February 2014 24: 212-226; Published in Advance November 21, 2013, doi:10.1101/gr.152132.112
      OPEN ACCESS ARTICLE

  2. Cazorla, Maite

    • Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia Genome Res. February 2014 24: 212-226; Published in Advance November 21, 2013, doi:10.1101/gr.152132.112
      OPEN ACCESS ARTICLE

  3. Chari, Sheila

    • Systematic mapping of occluded genes by cell fusion reveals prevalence and stability of cis-mediated silencing in somatic cells Genome Res. February 2014 24: 267-280; Published in Advance December 5, 2013, doi:10.1101/gr.143891.112

  4. Chen, Chih-Hsin

    • Systematic mapping of occluded genes by cell fusion reveals prevalence and stability of cis-mediated silencing in somatic cells Genome Res. February 2014 24: 267-280; Published in Advance December 5, 2013, doi:10.1101/gr.143891.112

  5. Chen, Ken

  6. Chen, Lei

  7. Chicken, Eric

  8. Cirkel, Geert A.

  9. Clift, Kayla L.

    • Systematic mapping of occluded genes by cell fusion reveals prevalence and stability of cis-mediated silencing in somatic cells Genome Res. February 2014 24: 267-280; Published in Advance December 5, 2013, doi:10.1101/gr.143891.112

  10. Clot, Guillem

    • Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia Genome Res. February 2014 24: 212-226; Published in Advance November 21, 2013, doi:10.1101/gr.152132.112
      OPEN ACCESS ARTICLE

  11. Colomer, Dolors

    • Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia Genome Res. February 2014 24: 212-226; Published in Advance November 21, 2013, doi:10.1101/gr.152132.112
      OPEN ACCESS ARTICLE

  12. Cuppen, Edwin

  13. Curley, Rebecca

    • Large-scale hypomethylated blocks associated with Epstein-Barr virus–induced B-cell immortalization Genome Res. February 2014 24: 177-184; Published in Advance September 25, 2013, doi:10.1101/gr.157743.113
      OPEN ACCESS ARTICLE

D

  1. Darst, Russell P.

    • Multiplex mapping of chromatin accessibility and DNA methylation within targeted single molecules identifies epigenetic heterogeneity in neural stem cells and glioblastoma Genome Res. February 2014 24: 329-339; Published in Advance October 8, 2013, doi:10.1101/gr.161737.113

  2. Davis, Ian J.

    • Variation in chromatin accessibility in human kidney cancer links H3K36 methyltransferase loss with widespread RNA processing defects Genome Res. February 2014 24: 241-250; Published in Advance October 24, 2013, doi:10.1101/gr.158253.113

  3. de Pagter, Mirjam S.

  4. Deleyrolle, Loic P.

    • Multiplex mapping of chromatin accessibility and DNA methylation within targeted single molecules identifies epigenetic heterogeneity in neural stem cells and glioblastoma Genome Res. February 2014 24: 329-339; Published in Advance October 8, 2013, doi:10.1101/gr.161737.113

  5. Dennis, Jonathan H.

  6. Ding, Li

  7. Djebali, Sarah

    • Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia Genome Res. February 2014 24: 212-226; Published in Advance November 21, 2013, doi:10.1101/gr.152132.112
      OPEN ACCESS ARTICLE

  8. Druliner, Brooke R.

  9. Duran, Karen

E

  1. Ecker, Joseph R.

    • Systematic mapping of occluded genes by cell fusion reveals prevalence and stability of cis-mediated silencing in somatic cells Genome Res. February 2014 24: 267-280; Published in Advance December 5, 2013, doi:10.1101/gr.143891.112

  2. Ecker, Simone

    • Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia Genome Res. February 2014 24: 212-226; Published in Advance November 21, 2013, doi:10.1101/gr.152132.112
      OPEN ACCESS ARTICLE

F

  1. Fan, Xian

  2. Faqeih, Eissa

  3. Faraji, Farhoud

    • An integrated systems genetics screen reveals the transcriptional structure of inherited predisposition to metastatic disease Genome Res. February 2014 24: 227-240; Published in Advance December 9, 2013, doi:10.1101/gr.166223.113

  4. Feinberg, Andrew P.

    • Large-scale hypomethylated blocks associated with Epstein-Barr virus–induced B-cell immortalization Genome Res. February 2014 24: 177-184; Published in Advance September 25, 2013, doi:10.1101/gr.157743.113
      OPEN ACCESS ARTICLE

  5. Feng, Jianxing

  6. Fernandes, Croydon J.

    • Systematic mapping of occluded genes by cell fusion reveals prevalence and stability of cis-mediated silencing in somatic cells Genome Res. February 2014 24: 267-280; Published in Advance December 5, 2013, doi:10.1101/gr.143891.112

  7. Ferreira, Pedro G.

    • Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia Genome Res. February 2014 24: 212-226; Published in Advance November 21, 2013, doi:10.1101/gr.152132.112
      OPEN ACCESS ARTICLE

  8. Fincher, Justin A.

  9. Foshay, Kara M.

    • Systematic mapping of occluded genes by cell fusion reveals prevalence and stability of cis-mediated silencing in somatic cells Genome Res. February 2014 24: 267-280; Published in Advance December 5, 2013, doi:10.1101/gr.143891.112

  10. Fu, Kai

  11. Furey, Terrence S.

    • Variation in chromatin accessibility in human kidney cancer links H3K36 methyltransferase loss with widespread RNA processing defects Genome Res. February 2014 24: 241-250; Published in Advance October 24, 2013, doi:10.1101/gr.158253.113

G

  1. Gaetz, Jedidiah

    • Systematic mapping of occluded genes by cell fusion reveals prevalence and stability of cis-mediated silencing in somatic cells Genome Res. February 2014 24: 267-280; Published in Advance December 5, 2013, doi:10.1101/gr.143891.112

  2. Ge, Ying

  3. Gilissen, Christian

    • Improved exome prioritization of disease genes through cross-species phenotype comparison Genome Res. February 2014 24: 340-348; Published in Advance October 25, 2013, doi:10.1101/gr.160325.113
      OPEN ACCESS ARTICLE

  4. Gillison, Maura L.

  5. Girimurugan, Senthil B.

  6. Goldberger, Natalie E.

    • An integrated systems genetics screen reveals the transcriptional structure of inherited predisposition to metastatic disease Genome Res. February 2014 24: 227-240; Published in Advance December 9, 2013, doi:10.1101/gr.166223.113

  7. Gómez-López, Gonzalo

    • Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia Genome Res. February 2014 24: 212-226; Published in Advance November 21, 2013, doi:10.1101/gr.152132.112
      OPEN ACCESS ARTICLE

  8. González-Pérez, Abel

    • Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia Genome Res. February 2014 24: 212-226; Published in Advance November 21, 2013, doi:10.1101/gr.152132.112
      OPEN ACCESS ARTICLE

  9. Gouin, Anaïs

    • Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia Genome Res. February 2014 24: 212-226; Published in Advance November 21, 2013, doi:10.1101/gr.152132.112
      OPEN ACCESS ARTICLE

  10. Grau, Daniel J.

  11. Guigó, Roderic

    • Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia Genome Res. February 2014 24: 212-226; Published in Advance November 21, 2013, doi:10.1101/gr.152132.112
      OPEN ACCESS ARTICLE

  12. Guipponi, Michel

    • Simultaneous identification and prioritization of variants in familial, de novo, and somatic genetic disorders with VariantMaster Genome Res. February 2014 24: 349-355; Published in Advance January 3, 2014, doi:10.1101/gr.163832.113

  13. Gupta, Shobhit

  14. Gut, Ivo

    • Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia Genome Res. February 2014 24: 212-226; Published in Advance November 21, 2013, doi:10.1101/gr.152132.112
      OPEN ACCESS ARTICLE

  15. Gut, Marta

    • Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia Genome Res. February 2014 24: 212-226; Published in Advance November 21, 2013, doi:10.1101/gr.152132.112
      OPEN ACCESS ARTICLE

  16. Guy, Tanisha

H

  1. Hacker, Kathryn E.

    • Variation in chromatin accessibility in human kidney cancer links H3K36 methyltransferase loss with widespread RNA processing defects Genome Res. February 2014 24: 241-250; Published in Advance October 24, 2013, doi:10.1101/gr.158253.113

  2. Haendel, Melissa

    • Improved exome prioritization of disease genes through cross-species phenotype comparison Genome Res. February 2014 24: 340-348; Published in Advance October 25, 2013, doi:10.1101/gr.160325.113
      OPEN ACCESS ARTICLE

  3. Hansen, Kasper D.

    • Large-scale hypomethylated blocks associated with Epstein-Barr virus–induced B-cell immortalization Genome Res. February 2014 24: 177-184; Published in Advance September 25, 2013, doi:10.1101/gr.157743.113
      OPEN ACCESS ARTICLE

  4. Harkins, Timothy T.

  5. He, Dandan

  6. Ho, Thai H.

    • Variation in chromatin accessibility in human kidney cancer links H3K36 methyltransferase loss with widespread RNA processing defects Genome Res. February 2014 24: 241-250; Published in Advance October 24, 2013, doi:10.1101/gr.158253.113

  7. Hoogstraat, Marlous

  8. Hu, Ying

    • An integrated systems genetics screen reveals the transcriptional structure of inherited predisposition to metastatic disease Genome Res. February 2014 24: 227-240; Published in Advance December 9, 2013, doi:10.1101/gr.166223.113

  9. Hunter, Kent W.

    • An integrated systems genetics screen reveals the transcriptional structure of inherited predisposition to metastatic disease Genome Res. February 2014 24: 227-240; Published in Advance December 9, 2013, doi:10.1101/gr.166223.113

J

  1. Jares, Pedro

    • Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia Genome Res. February 2014 24: 212-226; Published in Advance November 21, 2013, doi:10.1101/gr.152132.112
      OPEN ACCESS ARTICLE

  2. Jiang, Bo

  3. Johnson, Rory

    • Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia Genome Res. February 2014 24: 212-226; Published in Advance November 21, 2013, doi:10.1101/gr.152132.112
      OPEN ACCESS ARTICLE

  4. Jonasch, Eric

    • Variation in chromatin accessibility in human kidney cancer links H3K36 methyltransferase loss with widespread RNA processing defects Genome Res. February 2014 24: 241-250; Published in Advance October 24, 2013, doi:10.1101/gr.158253.113

  5. Jonges, Trudy N.

K

  1. Kingston, Robert E.

  2. Kladde, Michael P.

    • Multiplex mapping of chromatin accessibility and DNA methylation within targeted single molecules identifies epigenetic heterogeneity in neural stem cells and glioblastoma Genome Res. February 2014 24: 329-339; Published in Advance October 8, 2013, doi:10.1101/gr.161737.113

  3. Klein, Eva

    • Large-scale hypomethylated blocks associated with Epstein-Barr virus–induced B-cell immortalization Genome Res. February 2014 24: 177-184; Published in Advance September 25, 2013, doi:10.1101/gr.157743.113
      OPEN ACCESS ARTICLE

  4. Klein, Georg

    • Large-scale hypomethylated blocks associated with Epstein-Barr virus–induced B-cell immortalization Genome Res. February 2014 24: 177-184; Published in Advance September 25, 2013, doi:10.1101/gr.157743.113
      OPEN ACCESS ARTICLE

  5. Kloosterman, Wigard P.

  6. Knowles, David G.

    • Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia Genome Res. February 2014 24: 212-226; Published in Advance November 21, 2013, doi:10.1101/gr.152132.112
      OPEN ACCESS ARTICLE

  7. Köhler, Sebastian

    • Improved exome prioritization of disease genes through cross-species phenotype comparison Genome Res. February 2014 24: 340-348; Published in Advance October 25, 2013, doi:10.1101/gr.160325.113
      OPEN ACCESS ARTICLE

  8. Kong, Christina

  9. Koudijs, Marco J.

  10. Krawitz, Peter

    • Improved exome prioritization of disease genes through cross-species phenotype comparison Genome Res. February 2014 24: 340-348; Published in Advance October 25, 2013, doi:10.1101/gr.160325.113
      OPEN ACCESS ARTICLE

  11. Kreeftmeijer, Jennifer

  12. Kuan, Pei-Fen

    • Variation in chromatin accessibility in human kidney cancer links H3K36 methyltransferase loss with widespread RNA processing defects Genome Res. February 2014 24: 241-250; Published in Advance October 24, 2013, doi:10.1101/gr.158253.113

  13. Kulis, Marta

    • Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia Genome Res. February 2014 24: 212-226; Published in Advance November 21, 2013, doi:10.1101/gr.152132.112
      OPEN ACCESS ARTICLE

  14. Kumar, Bhavna

L

  1. Lahn, Bruce T.

    • Systematic mapping of occluded genes by cell fusion reveals prevalence and stability of cis-mediated silencing in somatic cells Genome Res. February 2014 24: 267-280; Published in Advance December 5, 2013, doi:10.1101/gr.143891.112

  2. Langmead, Ben

    • Large-scale hypomethylated blocks associated with Epstein-Barr virus–induced B-cell immortalization Genome Res. February 2014 24: 177-184; Published in Advance September 25, 2013, doi:10.1101/gr.157743.113
      OPEN ACCESS ARTICLE

  3. Le, Quynh-Thu

  4. Lee, Clarence C.

  5. Lee, Jae Hyun

    • Systematic mapping of occluded genes by cell fusion reveals prevalence and stability of cis-mediated silencing in somatic cells Genome Res. February 2014 24: 267-280; Published in Advance December 5, 2013, doi:10.1101/gr.143891.112

  6. Lewis, Suzanna E.

    • Improved exome prioritization of disease genes through cross-species phenotype comparison Genome Res. February 2014 24: 340-348; Published in Advance October 25, 2013, doi:10.1101/gr.160325.113
      OPEN ACCESS ARTICLE

  7. Li, Jingfeng

  8. Li, Wei-Qiang

    • Systematic mapping of occluded genes by cell fusion reveals prevalence and stability of cis-mediated silencing in somatic cells Genome Res. February 2014 24: 267-280; Published in Advance December 5, 2013, doi:10.1101/gr.143891.112

  9. Lieb, Jason D.

    • Variation in chromatin accessibility in human kidney cancer links H3K36 methyltransferase loss with widespread RNA processing defects Genome Res. February 2014 24: 241-250; Published in Advance October 24, 2013, doi:10.1101/gr.158253.113

  10. Lister, Ryan

    • Systematic mapping of occluded genes by cell fusion reveals prevalence and stability of cis-mediated silencing in somatic cells Genome Res. February 2014 24: 267-280; Published in Advance December 5, 2013, doi:10.1101/gr.143891.112

  11. Liu, X. Shirley

  12. Liu, Yu-Tsueng

  13. Lolkema, Martijn P.

  14. Looney, Timothy J.

    • Systematic mapping of occluded genes by cell fusion reveals prevalence and stability of cis-mediated silencing in somatic cells Genome Res. February 2014 24: 267-280; Published in Advance December 5, 2013, doi:10.1101/gr.143891.112

  15. López-Bigas, Nuria

    • Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia Genome Res. February 2014 24: 212-226; Published in Advance November 21, 2013, doi:10.1101/gr.152132.112
      OPEN ACCESS ARTICLE

  16. López-Guerra, Mónica

    • Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia Genome Res. February 2014 24: 212-226; Published in Advance November 21, 2013, doi:10.1101/gr.152132.112
      OPEN ACCESS ARTICLE

  17. López-Guillermo, Armando

    • Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia Genome Res. February 2014 24: 212-226; Published in Advance November 21, 2013, doi:10.1101/gr.152132.112
      OPEN ACCESS ARTICLE

  18. López-Otín, Carlos

    • Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia Genome Res. February 2014 24: 212-226; Published in Advance November 21, 2013, doi:10.1101/gr.152132.112
      OPEN ACCESS ARTICLE

M

  1. Makrythanasis, Periklis

    • Simultaneous identification and prioritization of variants in familial, de novo, and somatic genetic disorders with VariantMaster Genome Res. February 2014 24: 349-355; Published in Advance January 3, 2014, doi:10.1101/gr.163832.113

  2. Mao, Frank Fuxiang

    • Systematic mapping of occluded genes by cell fusion reveals prevalence and stability of cis-mediated silencing in somatic cells Genome Res. February 2014 24: 267-280; Published in Advance December 5, 2013, doi:10.1101/gr.143891.112

  3. Martínez-Trillos, Alejandra

    • Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia Genome Res. February 2014 24: 212-226; Published in Advance November 21, 2013, doi:10.1101/gr.152132.112
      OPEN ACCESS ARTICLE

  4. Martin-Subero, José Ignacio

    • Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia Genome Res. February 2014 24: 212-226; Published in Advance November 21, 2013, doi:10.1101/gr.152132.112
      OPEN ACCESS ARTICLE

  5. Michelini, Katelyn J.

    • Systematic mapping of occluded genes by cell fusion reveals prevalence and stability of cis-mediated silencing in somatic cells Genome Res. February 2014 24: 267-280; Published in Advance December 5, 2013, doi:10.1101/gr.143891.112

  6. Monlong, Jean

    • Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia Genome Res. February 2014 24: 212-226; Published in Advance November 21, 2013, doi:10.1101/gr.152132.112
      OPEN ACCESS ARTICLE

  7. Mungall, Christopher J.

    • Improved exome prioritization of disease genes through cross-species phenotype comparison Genome Res. February 2014 24: 340-348; Published in Advance October 25, 2013, doi:10.1101/gr.160325.113
      OPEN ACCESS ARTICLE

N

  1. Nabilsi, Nancy H.

    • Multiplex mapping of chromatin accessibility and DNA methylation within targeted single molecules identifies epigenetic heterogeneity in neural stem cells and glioblastoma Genome Res. February 2014 24: 329-339; Published in Advance October 8, 2013, doi:10.1101/gr.161737.113

  2. Nagy, Noemi

    • Large-scale hypomethylated blocks associated with Epstein-Barr virus–induced B-cell immortalization Genome Res. February 2014 24: 177-184; Published in Advance September 25, 2013, doi:10.1101/gr.157743.113
      OPEN ACCESS ARTICLE

  3. Nijman, Isaac J.

  4. Nikolaev, Sergey

    • Simultaneous identification and prioritization of variants in familial, de novo, and somatic genetic disorders with VariantMaster Genome Res. February 2014 24: 349-355; Published in Advance January 3, 2014, doi:10.1101/gr.163832.113

  5. Noble, William S.

O

  1. Oellrich, Anika

    • Improved exome prioritization of disease genes through cross-species phenotype comparison Genome Res. February 2014 24: 340-348; Published in Advance October 25, 2013, doi:10.1101/gr.160325.113
      OPEN ACCESS ARTICLE

P

  1. Padilla-Nash, Hesed

  2. Papasaikas, Panagiotis

    • Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia Genome Res. February 2014 24: 212-226; Published in Advance November 21, 2013, doi:10.1101/gr.152132.112
      OPEN ACCESS ARTICLE

  3. Park, Donghyun

    • Systematic mapping of occluded genes by cell fusion reveals prevalence and stability of cis-mediated silencing in somatic cells Genome Res. February 2014 24: 267-280; Published in Advance December 5, 2013, doi:10.1101/gr.143891.112

  4. Parker, Joel S.

    • Variation in chromatin accessibility in human kidney cancer links H3K36 methyltransferase loss with widespread RNA processing defects Genome Res. February 2014 24: 241-250; Published in Advance October 24, 2013, doi:10.1101/gr.158253.113

  5. Patel, Anand

  6. Pauli, Andrea

  7. Pelizzola, Mattia

    • Systematic mapping of occluded genes by cell fusion reveals prevalence and stability of cis-mediated silencing in somatic cells Genome Res. February 2014 24: 267-280; Published in Advance December 5, 2013, doi:10.1101/gr.143891.112

  8. Pinyol, Magda

    • Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia Genome Res. February 2014 24: 212-226; Published in Advance November 21, 2013, doi:10.1101/gr.152132.112
      OPEN ACCESS ARTICLE

  9. Pisano, David G.

    • Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia Genome Res. February 2014 24: 212-226; Published in Advance November 21, 2013, doi:10.1101/gr.152132.112
      OPEN ACCESS ARTICLE

  10. Prins, Jan F.

    • Variation in chromatin accessibility in human kidney cancer links H3K36 methyltransferase loss with widespread RNA processing defects Genome Res. February 2014 24: 241-250; Published in Advance October 24, 2013, doi:10.1101/gr.158253.113

  11. Puente, Xose S.

    • Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia Genome Res. February 2014 24: 212-226; Published in Advance November 21, 2013, doi:10.1101/gr.152132.112
      OPEN ACCESS ARTICLE

Q

  1. Qin, Jane Yuxia

    • Systematic mapping of occluded genes by cell fusion reveals prevalence and stability of cis-mediated silencing in somatic cells Genome Res. February 2014 24: 267-280; Published in Advance December 5, 2013, doi:10.1101/gr.143891.112

  2. Quesada, Victor

    • Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia Genome Res. February 2014 24: 212-226; Published in Advance November 21, 2013, doi:10.1101/gr.152132.112
      OPEN ACCESS ARTICLE

R

  1. Rathmell, W. Kimryn

    • Variation in chromatin accessibility in human kidney cancer links H3K36 methyltransferase loss with widespread RNA processing defects Genome Res. February 2014 24: 241-250; Published in Advance October 24, 2013, doi:10.1101/gr.158253.113

  2. Ren, Bing

    • Systematic mapping of occluded genes by cell fusion reveals prevalence and stability of cis-mediated silencing in somatic cells Genome Res. February 2014 24: 267-280; Published in Advance December 5, 2013, doi:10.1101/gr.143891.112

  3. Renkens, Ivo

  4. Reynolds, Brent A.

    • Multiplex mapping of chromatin accessibility and DNA methylation within targeted single molecules identifies epigenetic heterogeneity in neural stem cells and glioblastoma Genome Res. February 2014 24: 329-339; Published in Advance October 8, 2013, doi:10.1101/gr.161737.113

  5. Rico, Daniel

    • Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia Genome Res. February 2014 24: 212-226; Published in Advance November 21, 2013, doi:10.1101/gr.152132.112
      OPEN ACCESS ARTICLE

  6. Ried, Thomas

  7. Riva, Alberto

    • Multiplex mapping of chromatin accessibility and DNA methylation within targeted single molecules identifies epigenetic heterogeneity in neural stem cells and glioblastoma Genome Res. February 2014 24: 329-339; Published in Advance October 8, 2013, doi:10.1101/gr.161737.113

  8. Robinson, Peter N.

    • Improved exome prioritization of disease genes through cross-species phenotype comparison Genome Res. February 2014 24: 340-348; Published in Advance October 25, 2013, doi:10.1101/gr.160325.113
      OPEN ACCESS ARTICLE

  9. Robyr, Daniel

    • Simultaneous identification and prioritization of variants in familial, de novo, and somatic genetic disorders with VariantMaster Genome Res. February 2014 24: 349-355; Published in Advance January 3, 2014, doi:10.1101/gr.163832.113

  10. Rocco, James W.

  11. Royo, Cristina

    • Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia Genome Res. February 2014 24: 212-226; Published in Advance November 21, 2013, doi:10.1101/gr.152132.112
      OPEN ACCESS ARTICLE

  12. Rozman, Maria

    • Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia Genome Res. February 2014 24: 212-226; Published in Advance November 21, 2013, doi:10.1101/gr.152132.112
      OPEN ACCESS ARTICLE

S

  1. Sabunciyan, Sarven

    • Large-scale hypomethylated blocks associated with Epstein-Barr virus–induced B-cell immortalization Genome Res. February 2014 24: 177-184; Published in Advance September 25, 2013, doi:10.1101/gr.157743.113
      OPEN ACCESS ARTICLE

  2. Salamon, Daniel

    • Large-scale hypomethylated blocks associated with Epstein-Barr virus–induced B-cell immortalization Genome Res. February 2014 24: 177-184; Published in Advance September 25, 2013, doi:10.1101/gr.157743.113
      OPEN ACCESS ARTICLE

  3. Sanger Mouse Genetics Project

    • Improved exome prioritization of disease genes through cross-species phenotype comparison Genome Res. February 2014 24: 340-348; Published in Advance October 25, 2013, doi:10.1101/gr.160325.113
      OPEN ACCESS ARTICLE

  4. Santoni, Federico A.

    • Simultaneous identification and prioritization of variants in familial, de novo, and somatic genetic disorders with VariantMaster Genome Res. February 2014 24: 349-355; Published in Advance January 3, 2014, doi:10.1101/gr.163832.113

  5. Sauka-Spengler, Tatjana

  6. Schier, Alexander F.

  7. Schroth, Gary P.

    • Systematic mapping of occluded genes by cell fusion reveals prevalence and stability of cis-mediated silencing in somatic cells Genome Res. February 2014 24: 267-280; Published in Advance December 5, 2013, doi:10.1101/gr.143891.112

  8. Schwab, Richard

  9. Seelow, Dominik

    • Improved exome prioritization of disease genes through cross-species phenotype comparison Genome Res. February 2014 24: 340-348; Published in Advance October 25, 2013, doi:10.1101/gr.160325.113
      OPEN ACCESS ARTICLE

  10. Sexton, Brittany S.

  11. Shaheen, Ranad

  12. Sidow, Arend

  13. Simões-Costa, Marcos

  14. Simon, Jeremy M.

    • Variation in chromatin accessibility in human kidney cancer links H3K36 methyltransferase loss with widespread RNA processing defects Genome Res. February 2014 24: 241-250; Published in Advance October 24, 2013, doi:10.1101/gr.158253.113

  15. Singh, Darshan

    • Variation in chromatin accessibility in human kidney cancer links H3K36 methyltransferase loss with widespread RNA processing defects Genome Res. February 2014 24: 241-250; Published in Advance October 24, 2013, doi:10.1101/gr.158253.113

  16. Smedley, Damian

    • Improved exome prioritization of disease genes through cross-species phenotype comparison Genome Res. February 2014 24: 340-348; Published in Advance October 25, 2013, doi:10.1101/gr.160325.113
      OPEN ACCESS ARTICLE

  17. Sogaty, Sameera

  18. Stricker, Thomas

    • Systematic mapping of occluded genes by cell fusion reveals prevalence and stability of cis-mediated silencing in somatic cells Genome Res. February 2014 24: 267-280; Published in Advance December 5, 2013, doi:10.1101/gr.143891.112

  19. Sweeney, Robert T.

  20. Symer, David E.

T

  1. Tamborero, David

    • Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia Genome Res. February 2014 24: 212-226; Published in Advance November 21, 2013, doi:10.1101/gr.152132.112
      OPEN ACCESS ARTICLE

  2. Tan-Cabugao, Joanne

  3. Teknos, Theodoros N.

V

  1. Valencia, Alfonso

    • Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia Genome Res. February 2014 24: 212-226; Published in Advance November 21, 2013, doi:10.1101/gr.152132.112
      OPEN ACCESS ARTICLE

  2. Vallender, Eric J.

    • Systematic mapping of occluded genes by cell fusion reveals prevalence and stability of cis-mediated silencing in somatic cells Genome Res. February 2014 24: 267-280; Published in Advance December 5, 2013, doi:10.1101/gr.143891.112

  3. Valouev, Anton

  4. van Hummelen, Paul

  5. van Roosmalen, Markus J.

  6. van ’t Slot, Ruben

  7. Varma, Sushama

  8. Vastenhouw, Nadine L.

  9. Vera, Daniel L.

  10. Vihinen, Mauno

  11. Villamor, Neus

    • Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia Genome Res. February 2014 24: 212-226; Published in Advance November 21, 2013, doi:10.1101/gr.152132.112
      OPEN ACCESS ARTICLE

  12. Voest, Emile E.

W

  1. Wagner, Ulrich

    • Systematic mapping of occluded genes by cell fusion reveals prevalence and stability of cis-mediated silencing in somatic cells Genome Res. February 2014 24: 267-280; Published in Advance December 5, 2013, doi:10.1101/gr.143891.112

  2. Walker, Renard C.

    • An integrated systems genetics screen reveals the transcriptional structure of inherited predisposition to metastatic disease Genome Res. February 2014 24: 227-240; Published in Advance December 9, 2013, doi:10.1101/gr.166223.113

  3. Wallis, John

  4. Wang, Chenfei

  5. Wang, Kai

    • Improved exome prioritization of disease genes through cross-species phenotype comparison Genome Res. February 2014 24: 340-348; Published in Advance October 25, 2013, doi:10.1101/gr.160325.113
      OPEN ACCESS ARTICLE

  6. Wangsa, Danny

  7. Washington, Nicole

    • Improved exome prioritization of disease genes through cross-species phenotype comparison Genome Res. February 2014 24: 340-348; Published in Advance October 25, 2013, doi:10.1101/gr.160325.113
      OPEN ACCESS ARTICLE

  8. Weinstock, George

  9. Weiser, Matthew

    • Variation in chromatin accessibility in human kidney cancer links H3K36 methyltransferase loss with widespread RNA processing defects Genome Res. February 2014 24: 241-250; Published in Advance October 24, 2013, doi:10.1101/gr.158253.113

  10. Weng, Ziming

  11. West, Robert B.

  12. White, Kevin P.

    • Systematic mapping of occluded genes by cell fusion reveals prevalence and stability of cis-mediated silencing in somatic cells Genome Res. February 2014 24: 267-280; Published in Advance December 5, 2013, doi:10.1101/gr.143891.112

  13. Witteveen, Petronella O.

  14. Wu, Gang

    • An integrated systems genetics screen reveals the transcriptional structure of inherited predisposition to metastatic disease Genome Res. February 2014 24: 227-240; Published in Advance December 9, 2013, doi:10.1101/gr.166223.113

X

  1. Xiang, Andy Peng

    • Systematic mapping of occluded genes by cell fusion reveals prevalence and stability of cis-mediated silencing in somatic cells Genome Res. February 2014 24: 267-280; Published in Advance December 5, 2013, doi:10.1101/gr.143891.112

  2. Xiao, Weihong

Z

  1. Zhang, Jinfeng

  2. Zhang, Jinghui

    • An integrated systems genetics screen reveals the transcriptional structure of inherited predisposition to metastatic disease Genome Res. February 2014 24: 227-240; Published in Advance December 9, 2013, doi:10.1101/gr.166223.113

  3. Zhang, Li

    • Systematic mapping of occluded genes by cell fusion reveals prevalence and stability of cis-mediated silencing in somatic cells Genome Res. February 2014 24: 267-280; Published in Advance December 5, 2013, doi:10.1101/gr.143891.112

  4. Zhang, Lu

    • Systematic mapping of occluded genes by cell fusion reveals prevalence and stability of cis-mediated silencing in somatic cells Genome Res. February 2014 24: 267-280; Published in Advance December 5, 2013, doi:10.1101/gr.143891.112

  5. Zhang, Yong

  6. Zhang, Zhenyu

    • Systematic mapping of occluded genes by cell fusion reveals prevalence and stability of cis-mediated silencing in somatic cells Genome Res. February 2014 24: 267-280; Published in Advance December 5, 2013, doi:10.1101/gr.143891.112

  7. Zhou, Jie

    • Systematic mapping of occluded genes by cell fusion reveals prevalence and stability of cis-mediated silencing in somatic cells Genome Res. February 2014 24: 267-280; Published in Advance December 5, 2013, doi:10.1101/gr.143891.112

  8. Zhu, Fanxiu

  9. Zweemer, Ronald P.

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