Index by Author

April 2014; 24 (4)
  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. Alkan, Can

  2. Altemose, Nicolas

  3. Antonacci, Francesca

  4. Aplan, Peter D.

B

  1. Beckers, Johannes

    • Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon Genome Res. April 2014 24: 592-603; Published in Advance March 18, 2014, doi:10.1101/gr.166751.113
      OPEN ACCESS ARTICLE

  2. Bessa, José

    • Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon Genome Res. April 2014 24: 592-603; Published in Advance March 18, 2014, doi:10.1101/gr.166751.113
      OPEN ACCESS ARTICLE

C

  1. Canham, Natalie

    • A novel method for detecting uniparental disomy from trio genotypes identifies a significant excess in children with developmental disorders Genome Res. April 2014 24: 673-687; Published in Advance December 19, 2013, doi:10.1101/gr.160465.113

  2. Carninci, Piero

    • Comparison of CAGE and RNA-seq transcriptome profiling using clonally amplified and single-molecule next-generation sequencing Genome Res. April 2014 24: 708-717; Published in Advance March 27, 2014, doi:10.1101/gr.156232.113
      OPEN ACCESS ARTICLE

  3. Casares, Fernando

    • Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon Genome Res. April 2014 24: 592-603; Published in Advance March 18, 2014, doi:10.1101/gr.166751.113
      OPEN ACCESS ARTICLE

  4. Castoro, Ryan J.

  5. Cavalcoli, James D.

  6. Chaisson, Mark

  7. Chen, Qiang

  8. Chen, Songlin

  9. Chen, Yibin

  10. Chihara, Yoshitomo

  11. Claussnitzer, Melina

    • Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon Genome Res. April 2014 24: 592-603; Published in Advance March 18, 2014, doi:10.1101/gr.166751.113
      OPEN ACCESS ARTICLE

  12. Clayton-Smith, Jill

    • A novel method for detecting uniparental disomy from trio genotypes identifies a significant excess in children with developmental disorders Genome Res. April 2014 24: 673-687; Published in Advance December 19, 2013, doi:10.1101/gr.160465.113

  13. Court, Franck

    • Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment Genome Res. April 2014 24: 554-569; Published in Advance January 8, 2014, doi:10.1101/gr.164913.113

  14. Czamara, Darina

    • Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon Genome Res. April 2014 24: 592-603; Published in Advance March 18, 2014, doi:10.1101/gr.166751.113
      OPEN ACCESS ARTICLE

D

  1. Daneshmand, Siamak

  2. Dennis, Megan Y.

E

  1. Eichler, Evan E.

  2. Eskin, Eleazar

    • Identifying genetic relatives without compromising privacy Genome Res. April 2014 24: 664-672; Published in Advance March 10, 2014, doi:10.1101/gr.153346.112

  3. Estecio, Marcos R.H.

  4. Esteller, Manel

    • Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment Genome Res. April 2014 24: 554-569; Published in Advance January 8, 2014, doi:10.1101/gr.164913.113

F

  1. Fan, Qichang

    • A long-term demasculinization of X-linked intergenic noncoding RNAs in Drosophila melanogaster Genome Res. April 2014 24: 629-638; Published in Advance January 9, 2014, doi:10.1101/gr.165837.113
      OPEN ACCESS ARTICLE

  2. Fitzgerald, Tomas W.

    • A novel method for detecting uniparental disomy from trio genotypes identifies a significant excess in children with developmental disorders Genome Res. April 2014 24: 673-687; Published in Advance December 19, 2013, doi:10.1101/gr.160465.113

  3. Forrest, Alistair R.R.

    • Comparison of CAGE and RNA-seq transcriptome profiling using clonally amplified and single-molecule next-generation sequencing Genome Res. April 2014 24: 708-717; Published in Advance March 27, 2014, doi:10.1101/gr.156232.113
      OPEN ACCESS ARTICLE

  4. Fredman, David

  5. Fuchs, Helmut

    • Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon Genome Res. April 2014 24: 592-603; Published in Advance March 18, 2014, doi:10.1101/gr.166751.113
      OPEN ACCESS ARTICLE

  6. Furlotte, Nicholas A.

    • Identifying genetic relatives without compromising privacy Genome Res. April 2014 24: 664-672; Published in Advance March 10, 2014, doi:10.1101/gr.153346.112

G

  1. Gailus-Durner, Valérie

    • Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon Genome Res. April 2014 24: 592-603; Published in Advance March 18, 2014, doi:10.1101/gr.166751.113
      OPEN ACCESS ARTICLE

  2. Gao, Ge

    • A long-term demasculinization of X-linked intergenic noncoding RNAs in Drosophila melanogaster Genome Res. April 2014 24: 629-638; Published in Advance January 9, 2014, doi:10.1101/gr.165837.113
      OPEN ACCESS ARTICLE

  3. Garber, Manuel

  4. Garrett, Lillian

    • Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon Genome Res. April 2014 24: 592-603; Published in Advance March 18, 2014, doi:10.1101/gr.166751.113
      OPEN ACCESS ARTICLE

  5. Gieger, Christian

    • Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon Genome Res. April 2014 24: 592-603; Published in Advance March 18, 2014, doi:10.1101/gr.166751.113
      OPEN ACCESS ARTICLE

  6. Giesert, Florian

    • Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon Genome Res. April 2014 24: 592-603; Published in Advance March 18, 2014, doi:10.1101/gr.166751.113
      OPEN ACCESS ARTICLE

  7. Gilles, Anna F.

  8. Gómez-Skarmeta, Jose Luis

    • Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon Genome Res. April 2014 24: 592-603; Published in Advance March 18, 2014, doi:10.1101/gr.166751.113
      OPEN ACCESS ARTICLE

  9. Gough, Sheryl M.

  10. Graves, Tina A.

H

  1. Harness, Julie V.

    • Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment Genome Res. April 2014 24: 554-569; Published in Advance January 8, 2014, doi:10.1101/gr.164913.113

  2. Hata, Kenichiro

    • Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment Genome Res. April 2014 24: 554-569; Published in Advance January 8, 2014, doi:10.1101/gr.164913.113

  3. Hauck, Stefanie M.

    • Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon Genome Res. April 2014 24: 592-603; Published in Advance March 18, 2014, doi:10.1101/gr.166751.113
      OPEN ACCESS ARTICLE

  4. Hayashizaki, Yoshihide

    • Comparison of CAGE and RNA-seq transcriptome profiling using clonally amplified and single-molecule next-generation sequencing Genome Res. April 2014 24: 708-717; Published in Advance March 27, 2014, doi:10.1101/gr.156232.113
      OPEN ACCESS ARTICLE

  5. He, Dan

    • Identifying genetic relatives without compromising privacy Genome Res. April 2014 24: 664-672; Published in Advance March 10, 2014, doi:10.1101/gr.153346.112

  6. Hölter, Sabine M.

    • Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon Genome Res. April 2014 24: 592-603; Published in Advance March 18, 2014, doi:10.1101/gr.166751.113
      OPEN ACCESS ARTICLE

  7. Hon, Lawrence

  8. Hormozdiari, Farhad

    • Identifying genetic relatives without compromising privacy Genome Res. April 2014 24: 664-672; Published in Advance March 10, 2014, doi:10.1101/gr.153346.112

  9. Horsch, Marion

    • Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon Genome Res. April 2014 24: 592-603; Published in Advance March 18, 2014, doi:10.1101/gr.166751.113
      OPEN ACCESS ARTICLE

  10. Hrabě de Angelis, Martin

    • Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon Genome Res. April 2014 24: 592-603; Published in Advance March 18, 2014, doi:10.1101/gr.166751.113
      OPEN ACCESS ARTICLE

  11. Hu, Qiaomu

  12. Huddleston, John

  13. Hurles, Matthew E.

    • A novel method for detecting uniparental disomy from trio genotypes identifies a significant excess in children with developmental disorders Genome Res. April 2014 24: 673-687; Published in Advance December 19, 2013, doi:10.1101/gr.160465.113

I

  1. Iglesias-Platas, Isabel

    • Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment Genome Res. April 2014 24: 554-569; Published in Advance January 8, 2014, doi:10.1101/gr.164913.113

  2. Ishikawa-Kato, Sachi

    • Comparison of CAGE and RNA-seq transcriptome profiling using clonally amplified and single-molecule next-generation sequencing Genome Res. April 2014 24: 708-717; Published in Advance March 27, 2014, doi:10.1101/gr.156232.113
      OPEN ACCESS ARTICLE

  3. Issa, Jean-Pierre J.

  4. Itoh, Masayoshi

    • Comparison of CAGE and RNA-seq transcriptome profiling using clonally amplified and single-molecule next-generation sequencing Genome Res. April 2014 24: 708-717; Published in Advance March 27, 2014, doi:10.1101/gr.156232.113
      OPEN ACCESS ARTICLE

J

  1. Jain, Miten

  2. Jelinek, Jaroslav

  3. Jin, Lijun

  4. Jin, Zonghui

  5. Johnson, Diana

    • A novel method for detecting uniparental disomy from trio genotypes identifies a significant excess in children with developmental disorders Genome Res. April 2014 24: 673-687; Published in Advance December 19, 2013, doi:10.1101/gr.160465.113

  6. Jones, Peter A.

  7. Joo, Jong Wha J.

    • Identifying genetic relatives without compromising privacy Genome Res. April 2014 24: 664-672; Published in Advance March 10, 2014, doi:10.1101/gr.153346.112

K

  1. Kaffe, Maria

    • Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon Genome Res. April 2014 24: 592-603; Published in Advance March 18, 2014, doi:10.1101/gr.166751.113
      OPEN ACCESS ARTICLE

  2. Kaiho, Ai

    • Comparison of CAGE and RNA-seq transcriptome profiling using clonally amplified and single-molecule next-generation sequencing Genome Res. April 2014 24: 708-717; Published in Advance March 27, 2014, doi:10.1101/gr.156232.113
      OPEN ACCESS ARTICLE

  3. Kanamori-Katayama, Mutsumi

    • Comparison of CAGE and RNA-seq transcriptome profiling using clonally amplified and single-molecule next-generation sequencing Genome Res. April 2014 24: 708-717; Published in Advance March 27, 2014, doi:10.1101/gr.156232.113
      OPEN ACCESS ARTICLE

  4. Kaneki, Eisuke

    • Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment Genome Res. April 2014 24: 554-569; Published in Advance January 8, 2014, doi:10.1101/gr.164913.113

  5. Karbalai, Nazanin

    • Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon Genome Res. April 2014 24: 592-603; Published in Advance March 18, 2014, doi:10.1101/gr.166751.113
      OPEN ACCESS ARTICLE

  6. Kawaji, Hideya

    • Comparison of CAGE and RNA-seq transcriptome profiling using clonally amplified and single-molecule next-generation sequencing Genome Res. April 2014 24: 708-717; Published in Advance March 27, 2014, doi:10.1101/gr.156232.113
      OPEN ACCESS ARTICLE

  7. Kawano, Mitsuoki

    • Comparison of CAGE and RNA-seq transcriptome profiling using clonally amplified and single-molecule next-generation sequencing Genome Res. April 2014 24: 708-717; Published in Advance March 27, 2014, doi:10.1101/gr.156232.113
      OPEN ACCESS ARTICLE

  8. Keirstead, Hans

    • Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment Genome Res. April 2014 24: 554-569; Published in Advance January 8, 2014, doi:10.1101/gr.164913.113

  9. Kellis, Manolis

  10. Kent, W. James

  11. King, Daniel A.

    • A novel method for detecting uniparental disomy from trio genotypes identifies a significant excess in children with developmental disorders Genome Res. April 2014 24: 673-687; Published in Advance December 19, 2013, doi:10.1101/gr.160465.113

  12. Kitamura, Toshio

  13. Klingenspor, Martin

    • Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon Genome Res. April 2014 24: 592-603; Published in Advance March 18, 2014, doi:10.1101/gr.166751.113
      OPEN ACCESS ARTICLE

  14. Knauf, Franziska

    • Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon Genome Res. April 2014 24: 592-603; Published in Advance March 18, 2014, doi:10.1101/gr.166751.113
      OPEN ACCESS ARTICLE

  15. Kojima-Ishiyama, Miki

    • Comparison of CAGE and RNA-seq transcriptome profiling using clonally amplified and single-molecule next-generation sequencing Genome Res. April 2014 24: 708-717; Published in Advance March 27, 2014, doi:10.1101/gr.156232.113
      OPEN ACCESS ARTICLE

  16. Korlach, Jonas

L

  1. Lapunzina, Pablo

    • Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment Genome Res. April 2014 24: 554-569; Published in Advance January 8, 2014, doi:10.1101/gr.164913.113

  2. Laumen, Helmut

    • Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon Genome Res. April 2014 24: 592-603; Published in Advance March 18, 2014, doi:10.1101/gr.166751.113
      OPEN ACCESS ARTICLE

  3. Lay, Fides D.

  4. Lee, Heekyoung

    • Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon Genome Res. April 2014 24: 592-603; Published in Advance March 18, 2014, doi:10.1101/gr.166751.113
      OPEN ACCESS ARTICLE

  5. Li, Qiye

  6. Li, Xin Z.

  7. Li, Xinmin

    • A long-term demasculinization of X-linked intergenic noncoding RNAs in Drosophila melanogaster Genome Res. April 2014 24: 629-638; Published in Advance January 9, 2014, doi:10.1101/gr.165837.113
      OPEN ACCESS ARTICLE

  8. Li, Yangzhen

  9. Li, Zheng

    • A long-term demasculinization of X-linked intergenic noncoding RNAs in Drosophila melanogaster Genome Res. April 2014 24: 629-638; Published in Advance January 9, 2014, doi:10.1101/gr.165837.113
      OPEN ACCESS ARTICLE

  10. Lian, Jinmin

  11. Liang, Gangning

  12. Liang, Shoudan

  13. Liang, Zhuo

  14. Lichtner, Peter

    • Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon Genome Res. April 2014 24: 592-603; Published in Advance March 18, 2014, doi:10.1101/gr.166751.113
      OPEN ACCESS ARTICLE

  15. Liu, Ming

    • A long-term demasculinization of X-linked intergenic noncoding RNAs in Drosophila melanogaster Genome Res. April 2014 24: 629-638; Published in Advance January 9, 2014, doi:10.1101/gr.165837.113
      OPEN ACCESS ARTICLE

  16. Liu, Shanshan

  17. Lizio, Marina

    • Comparison of CAGE and RNA-seq transcriptome profiling using clonally amplified and single-molecule next-generation sequencing Genome Res. April 2014 24: 708-717; Published in Advance March 27, 2014, doi:10.1101/gr.156232.113
      OPEN ACCESS ARTICLE

  18. Long, Manyuan

    • A long-term demasculinization of X-linked intergenic noncoding RNAs in Drosophila melanogaster Genome Res. April 2014 24: 629-638; Published in Advance January 9, 2014, doi:10.1101/gr.165837.113
      OPEN ACCESS ARTICLE

  19. Lu, Yue

M

  1. Maegawa, Shinji

  2. Malig, Maika

  3. Mansour, Sahar

    • A novel method for detecting uniparental disomy from trio genotypes identifies a significant excess in children with developmental disorders Genome Res. April 2014 24: 673-687; Published in Advance December 19, 2013, doi:10.1101/gr.160465.113

  4. Martin, Sue Ellen

  5. Martin-Trujillo, Alex

    • Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment Genome Res. April 2014 24: 554-569; Published in Advance January 8, 2014, doi:10.1101/gr.164913.113

  6. McEachin, Richard C.

  7. Meitinger, Thomas

    • Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon Genome Res. April 2014 24: 592-603; Published in Advance March 18, 2014, doi:10.1101/gr.166751.113
      OPEN ACCESS ARTICLE

  8. Miga, Karen H.

  9. Miller, Ray

    • A novel method for detecting uniparental disomy from trio genotypes identifies a significant excess in children with developmental disorders Genome Res. April 2014 24: 673-687; Published in Advance December 19, 2013, doi:10.1101/gr.160465.113

  10. Monk, David

    • Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment Genome Res. April 2014 24: 554-569; Published in Advance January 8, 2014, doi:10.1101/gr.164913.113

  11. Moore, Harry

    • Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment Genome Res. April 2014 24: 554-569; Published in Advance January 8, 2014, doi:10.1101/gr.164913.113

  12. Moran, Yehu

  13. Müller-Myhsok, Bertram

    • Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon Genome Res. April 2014 24: 592-603; Published in Advance March 18, 2014, doi:10.1101/gr.166751.113
      OPEN ACCESS ARTICLE

  14. Murata, Mitsuyoshi

    • Comparison of CAGE and RNA-seq transcriptome profiling using clonally amplified and single-molecule next-generation sequencing Genome Res. April 2014 24: 708-717; Published in Advance March 27, 2014, doi:10.1101/gr.156232.113
      OPEN ACCESS ARTICLE

N

  1. Nagao-Sato, Sayaka

    • Comparison of CAGE and RNA-seq transcriptome profiling using clonally amplified and single-molecule next-generation sequencing Genome Res. April 2014 24: 708-717; Published in Advance March 27, 2014, doi:10.1101/gr.156232.113
      OPEN ACCESS ARTICLE

  2. Nakabayashi, Kazuhiko

    • Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment Genome Res. April 2014 24: 554-569; Published in Advance January 8, 2014, doi:10.1101/gr.164913.113

  3. Naumann, Ronald

    • Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon Genome Res. April 2014 24: 592-603; Published in Advance March 18, 2014, doi:10.1101/gr.166751.113
      OPEN ACCESS ARTICLE

  4. Newton, Yulia

  5. Ninomiya-Fukuda, Noriko

    • Comparison of CAGE and RNA-seq transcriptome profiling using clonally amplified and single-molecule next-generation sequencing Genome Res. April 2014 24: 708-717; Published in Advance March 27, 2014, doi:10.1101/gr.156232.113
      OPEN ACCESS ARTICLE

  6. Nishiyori-Sueki, Hiromi

    • Comparison of CAGE and RNA-seq transcriptome profiling using clonally amplified and single-molecule next-generation sequencing Genome Res. April 2014 24: 708-717; Published in Advance March 27, 2014, doi:10.1101/gr.156232.113
      OPEN ACCESS ARTICLE

  7. Noma, Shohei

    • Comparison of CAGE and RNA-seq transcriptome profiling using clonally amplified and single-molecule next-generation sequencing Genome Res. April 2014 24: 708-717; Published in Advance March 27, 2014, doi:10.1101/gr.156232.113
      OPEN ACCESS ARTICLE

O

  1. Ogata, Tsutomu

    • Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment Genome Res. April 2014 24: 554-569; Published in Advance January 8, 2014, doi:10.1101/gr.164913.113

  2. Okamura, Kohji

    • Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment Genome Res. April 2014 24: 554-569; Published in Advance January 8, 2014, doi:10.1101/gr.164913.113

  3. Ostrovsky, Rafail

    • Identifying genetic relatives without compromising privacy Genome Res. April 2014 24: 664-672; Published in Advance March 10, 2014, doi:10.1101/gr.153346.112

P

  1. Praher, Daniela

  2. Pribitzer, Carina

R

  1. Ranade, Swati

  2. Rendeiro, André F.

  3. Renfer, Eduard

  4. Rentzsch, Fabian

  5. Roe, Bruce A.

  6. Romanelli, Valeria

    • Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment Genome Res. April 2014 24: 554-569; Published in Advance January 8, 2014, doi:10.1101/gr.164913.113

  7. Rozman, Jan

    • Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon Genome Res. April 2014 24: 592-603; Published in Advance March 18, 2014, doi:10.1101/gr.166751.113
      OPEN ACCESS ARTICLE

S

  1. Sahai, Amit

    • Identifying genetic relatives without compromising privacy Genome Res. April 2014 24: 664-672; Published in Advance March 10, 2014, doi:10.1101/gr.153346.112

  2. Sanchez-Mut, Jose Vicente

    • Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment Genome Res. April 2014 24: 554-569; Published in Advance January 8, 2014, doi:10.1101/gr.164913.113

  3. Schauer, Alexandra

  4. Schinko, Johannes B.

  5. Schönauer, Anna

  6. Schormair, Barbara

    • Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon Genome Res. April 2014 24: 592-603; Published in Advance March 18, 2014, doi:10.1101/gr.166751.113
      OPEN ACCESS ARTICLE

  7. Schwaiger, Michaela

  8. Seitz, Hervé

  9. Shao, Changwei

  10. Shin, Jay W.

    • Comparison of CAGE and RNA-seq transcriptome profiling using clonally amplified and single-molecule next-generation sequencing Genome Res. April 2014 24: 708-717; Published in Advance March 27, 2014, doi:10.1101/gr.156232.113
      OPEN ACCESS ARTICLE

  11. Simón, Carlos

    • Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment Genome Res. April 2014 24: 554-569; Published in Advance January 8, 2014, doi:10.1101/gr.164913.113

  12. Skinner, Eila C.

  13. Soejima, Hidenobu

    • Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment Genome Res. April 2014 24: 554-569; Published in Advance January 8, 2014, doi:10.1101/gr.164913.113

  14. Spieler, Derek

    • Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon Genome Res. April 2014 24: 592-603; Published in Advance March 18, 2014, doi:10.1101/gr.166751.113
      OPEN ACCESS ARTICLE

  15. Stewart, Fiona

    • A novel method for detecting uniparental disomy from trio genotypes identifies a significant excess in children with developmental disorders Genome Res. April 2014 24: 673-687; Published in Advance December 19, 2013, doi:10.1101/gr.160465.113

  16. Su, Sheng-Fang

  17. Sudmant, Peter H.

  18. Sugahara, Naoko

    • Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment Genome Res. April 2014 24: 554-569; Published in Advance January 8, 2014, doi:10.1101/gr.164913.113

  19. Sun, Bing

T

  1. Tayama, Chiharu

    • Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment Genome Res. April 2014 24: 554-569; Published in Advance January 8, 2014, doi:10.1101/gr.164913.113

  2. Technau, Ulrich

  3. Tena, Juan J.

    • Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon Genome Res. April 2014 24: 592-603; Published in Advance March 18, 2014, doi:10.1101/gr.166751.113
      OPEN ACCESS ARTICLE

  4. the DDD Study

    • A novel method for detecting uniparental disomy from trio genotypes identifies a significant excess in children with developmental disorders Genome Res. April 2014 24: 673-687; Published in Advance December 19, 2013, doi:10.1101/gr.160465.113

  5. The FANTOM Consortium

    • Comparison of CAGE and RNA-seq transcriptome profiling using clonally amplified and single-molecule next-generation sequencing Genome Res. April 2014 24: 708-717; Published in Advance March 27, 2014, doi:10.1101/gr.156232.113
      OPEN ACCESS ARTICLE

  6. Tilch, Erik

    • Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon Genome Res. April 2014 24: 592-603; Published in Advance March 18, 2014, doi:10.1101/gr.166751.113
      OPEN ACCESS ARTICLE

  7. Torres, Miguel

    • Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon Genome Res. April 2014 24: 592-603; Published in Advance March 18, 2014, doi:10.1101/gr.166751.113
      OPEN ACCESS ARTICLE

  8. Triche, Timothy J., Jr.

  9. Tsai, Yvonne C.

  10. Turner, Stephen W.

V

  1. VanKuren, Nicholas W.

    • A long-term demasculinization of X-linked intergenic noncoding RNAs in Drosophila melanogaster Genome Res. April 2014 24: 629-638; Published in Advance January 9, 2014, doi:10.1101/gr.165837.113
      OPEN ACCESS ARTICLE

  2. Vasudevan, Pradeep

    • A novel method for detecting uniparental disomy from trio genotypes identifies a significant excess in children with developmental disorders Genome Res. April 2014 24: 673-687; Published in Advance December 19, 2013, doi:10.1101/gr.160465.113

  3. Vibranovski, Maria D.

    • A long-term demasculinization of X-linked intergenic noncoding RNAs in Drosophila melanogaster Genome Res. April 2014 24: 629-638; Published in Advance January 9, 2014, doi:10.1101/gr.165837.113
      OPEN ACCESS ARTICLE

  4. von Toerne, Christine

    • Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon Genome Res. April 2014 24: 592-603; Published in Advance March 18, 2014, doi:10.1101/gr.166751.113
      OPEN ACCESS ARTICLE

W

  1. Wadia, Akshay

    • Identifying genetic relatives without compromising privacy Genome Res. April 2014 24: 664-672; Published in Advance March 10, 2014, doi:10.1101/gr.153346.112

  2. Wake, Norio

    • Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment Genome Res. April 2014 24: 554-569; Published in Advance January 8, 2014, doi:10.1101/gr.164913.113

  3. Waldenberger, Melanie

    • Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon Genome Res. April 2014 24: 592-603; Published in Advance March 18, 2014, doi:10.1101/gr.166751.113
      OPEN ACCESS ARTICLE

  4. Wang, Jun

  5. Wang, Zongji

  6. Washietl, Stefan

  7. Watanabe-Okochi, Naoko

  8. Wee, Liang Meng

  9. Wei, Liping

    • A long-term demasculinization of X-linked intergenic noncoding RNAs in Drosophila melanogaster Genome Res. April 2014 24: 629-638; Published in Advance January 9, 2014, doi:10.1101/gr.165837.113
      OPEN ACCESS ARTICLE

  10. Willard, Huntington F.

  11. Wilson, Richard K.

  12. Winkelmann, Juliane

    • Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon Genome Res. April 2014 24: 592-603; Published in Advance March 18, 2014, doi:10.1101/gr.166751.113
      OPEN ACCESS ARTICLE

  13. Wurst, Wolfgang

    • Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon Genome Res. April 2014 24: 592-603; Published in Advance March 18, 2014, doi:10.1101/gr.166751.113
      OPEN ACCESS ARTICLE

Y

  1. Yu, Xiaochun

Z

  1. Zamore, Phillip D.

  2. Zhang, Guojie

  3. Zhang, Li

    • A long-term demasculinization of X-linked intergenic noncoding RNAs in Drosophila melanogaster Genome Res. April 2014 24: 629-638; Published in Advance January 9, 2014, doi:10.1101/gr.165837.113
      OPEN ACCESS ARTICLE

  4. Zhang, Nianxiang

  5. Zhang, Pei

  6. Zhang, Wenxia

    • A long-term demasculinization of X-linked intergenic noncoding RNAs in Drosophila melanogaster Genome Res. April 2014 24: 629-638; Published in Advance January 9, 2014, doi:10.1101/gr.165837.113
      OPEN ACCESS ARTICLE

  7. Zhang, Yong

  8. Zhang, Yong E.

    • A long-term demasculinization of X-linked intergenic noncoding RNAs in Drosophila melanogaster Genome Res. April 2014 24: 629-638; Published in Advance January 9, 2014, doi:10.1101/gr.165837.113
      OPEN ACCESS ARTICLE

  9. Zhao, Hongmei

  10. Zheng, Qiumei

Current Issue

  1. January 2026, 36 (1)
  1. Current Issue
  1. Alert me to new issues of Genome Research