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Alice Yamada

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Kiichiro Tomoda; Peter Tsang; Mark P White; N Alice Yamada; Shiro Baba; Bruce R Conklin; Kirsten E Eilertson; Karen Leung; Megumi Narita; Aki Okada; Barbara Panning; Salma Sami; Deepak Srivastava; Kazutoshi Takahashi; Shinya Yamanaka
Derivation conditions impact X-inactivation status in female human induced pluripotent stem cells.
Jeffrey M Kidd; Nick Sampas; Francesca Antonacci; Tina Graves; Robert Fulton; Hillary S Hayden; Can Alkan; Maika Malig; Mario Ventura; Giuliana Giannuzzi; Joelle Kallicki; Paige Anderson; Anya Tsalenko; N Alice Yamada; Peter Tsang; Rajinder Kaul; Richard K Wilson; Laurakay Bruhn; Evan E Eichler
Characterization of missing human genome sequences and copy-number polymorphic insertions.
George H Perry; Amir Ben-Dor; Anya Tsalenko; Nick Sampas; Laia Rodriguez-Revenga; Charles W Tran; Alicia Scheffer; Israel Steinfeld; Peter Tsang; N Alice Yamada; Han Soo Park; Jong-Il Kim; Jeong-Sun Seo; Zohar Yakhini; Stephen Laderman; Laurakay Bruhn; Charles Lee
The fine-scale and complex architecture of human copy-number variation.

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All Publications

2012: Kiichiro Tomoda; Peter Tsang; Mark P White; N Alice Yamada; Shiro Baba; Bruce R Conklin; Kirsten E Eilertson; Karen Leung; Megumi Narita; Aki Okada; Barbara Panning; Salma Sami; Deepak Srivastava; Kazutoshi Takahashi; Shinya Yamanaka
Derivation conditions impact X-inactivation status in female human induced pluripotent stem cells.
Cell stem cell 2012;11(1):91-9.
2010: Jeffrey M Kidd; Nick Sampas; Francesca Antonacci; Tina Graves; Robert Fulton; Hillary S Hayden; Can Alkan; Maika Malig; Mario Ventura; Giuliana Giannuzzi; Joelle Kallicki; Paige Anderson; Anya Tsalenko; N Alice Yamada; Peter Tsang; Rajinder Kaul; Richard K Wilson; Laurakay Bruhn; Evan E Eichler
Characterization of missing human genome sequences and copy-number polymorphic insertions.
Nature methods 2010;7(5):365-71.
2008: George H Perry; Amir Ben-Dor; Anya Tsalenko; Nick Sampas; Laia Rodriguez-Revenga; Charles W Tran; Alicia Scheffer; Israel Steinfeld; Peter Tsang; N Alice Yamada; Han Soo Park; Jong-Il Kim; Jeong-Sun Seo; Zohar Yakhini; Stephen Laderman; Laurakay Bruhn; Charles Lee
The fine-scale and complex architecture of human copy-number variation.
American journal of human genetics 2008;82(3):685-95.
2008: Colleen Elso; Xiaochen Lu; Stephanie Morrison; Angela Tarver; Heather Thompson; Hillary Thurkow; N Alice Yamada; Lisa Stubbs
Germline translocations in mice: unique tools for analyzing gene function and long-distance regulatory mechanisms.
Journal of the National Cancer Institute. Monographs 2008;(39):91-5.
2007: Adam J de Smith; Anya Tsalenko; Nick Sampas; Alicia Scheffer; N Alice Yamada; Peter Tsang; Amir Ben-Dor; Zohar Yakhini; Richard J Ellis; Laurakay Bruhn; Stephen Laderman; philippe froguel; Alexandra I F Blakemore
Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males: implications for association studies of complex diseases.
Human molecular genetics 2007;16(23):2783-94.
2006: John M Hinz; Peter B Nham; N Alice Yamada; Robert S Tebbs; Edmund P Salazar; Angela K Hinz; Harvey W Mohrenweiser; Irene M Jones; Larry H Thompson
Four human FANCG polymorphic variants show normal biological function in hamster CHO cells.
Mutation research 2006;602(1-2):34-42.
2005: John M Hinz; N Alice Yamada; Edmund P Salazar; Robert S Tebbs; Larry H Thompson
Influence of double-strand-break repair pathways on radiosensitivity throughout the cell cycle in CHO cells.
DNA repair 2005;4(7):782-92.
2005: Larry H Thompson; John M Hinz; N Alice Yamada; Nigel Jones
How Fanconi anemia proteins promote the four Rs: replication, recombination, repair, and recovery.
Environmental and molecular mutagenesis 2005;45(2-3):128-42.
2005: Robert S Tebbs; John M Hinz; N Alice Yamada; James B Wilson; Edmund P Salazar; Cynthia B Thomas; Irene M Jones; Nigel Jones; Larry H Thompson
New insights into the Fanconi anemia pathway from an isogenic FancG hamster CHO mutant.
DNA repair 2005;4(1):11-22.
2005: Kristi A Miller; John M Hinz; N Alice Yamada; Larry H Thompson; Joanna S Albala
Nuclear localization of Rad51B is independent of Rad51C and BRCA2.
Mutagenesis 2005;20(1):57-63.