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E

Emily H. Turner

university of washington
H指数:32
被引数:1.3万

个人简介

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工作经历

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荣誉奖项

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Improving performance of multigene panels for genomic analysis of cancer predisposition
GENETICS IN MEDICINE
IF6.2
2016-10-0173
OAAI
Shirts, Brian H.; Casadei, Silvia; Jacobson, Angela L.; Lee, Ming K.; Gulsuner, Suleyman; Bennett, Robin L.; Miller, Margaret; Hall, Sarah A.; Hampel, Heather; Hisama, Fuki M.; Naylor, Lorraine V.; Goetsch, Cathleen; Leppig, Kathleen; Tait, Jonathan F.; Scroggins, Sheena M.; Turner, Emily H.; Livingston, Robert; Salipante, Stephen J.; King, Mary-Claire; Walsh, Tom; Pritchard, Colin C.
Frequent PIK3CA Mutations in Colorectal and Endometrial Tumors With 2 or More Somatic Mutations in Mismatch Repair Genes
GASTROENTEROLOGY
IF25.1
2016-09-0136
OAAI
Cohen, Stacey A.; Turner, Emily H.; Beightol, Mallory B.; Jacobson, Angela; Gooley, Ted A.; Salipante, Stephen J.; Haraldsdottir, Sigurdis; Smith, Christina; Scroggins, Sheena; Tait, Jonathan F.; Grady, William M.; Lin, Edward H.; Cohn, David E.; Goodfellow, Paul J.; Arnold, Mark W.; de la Chapelle, Albert; Pearlman, Rachel; Hampel, Heather; Pritchard, Colin C.
Actionable exomic incidental findings in 6503 participants: challenges of variant classification

6503参与者中可行的exomic偶然发现: 变异分类的挑战

GENOME RESEARCH
IF5.5
2015-01-30304
OAAI
Amendola, Laura M.; Dorschner, Michael O.; Robertson, Peggy D.; Salama, Joseph S.; Hart, Ragan; Shirts, Brian H.; Murray, Mitzi L.; Tokita, Mari J.; Gallego, Carlos J.; Kim, Daniel Seung; Bennett, James T.; Crosslin, David R.; Ranchalis, Jane; Jones, Kelly L.; Rosenthal, Elisabeth A.; Jarvik, Ella R.; Itsara, Andy; Turner, Emily H.; Herman, Daniel S.; Schleit, Jennifer; Burt, Amber; Jamal, Seema M.; Abrudan, Jenica L.; Johnson, Andrew D.; Conlin, Laura K.; Dulik, Matthew C.; Santani, Avni; Metterville, Danielle R.; Kelly, Melissa; Foreman, Ann Katherine M.; Lee, Kristy; Taylor, Kent D.; Guo, Xiuqing; Crooks, Kristy; Kiedrowski, Lesli A.; Raffe, Leslie J.; Gordon, Ora; Machini, Kalotina; Desnick, Robe; Biesecker, Leslie G.; Lubitz, Steven A.; Mulchandani, Surabhi; Cooper, Greg M.; Joffe, Steven; Richards, C. Sue; Yang, Yaoping; Rotter, Jerome I.; Rich, Stephen S.; O'Donne, Christopher J.; Berg, Jonathan S.; Spinner, Nancy B.; Evans, James P.; Fullerton, Stephanie M.; Leppig, Kathleen A.; Bennett, Robin L.; Bird, Thomas; Sybert, Virginia P.; Grady, William M.; Tabor, Holly K.; Kim, Jerry H.; Bamshad, Michael J.; Wilfond, Benjamin; Motulsky, Arno G.; Scott, Ronald; Pritchard, Colin C.; Walsh, Tom D.; Burke, Wylie; Raskind, Wendy H.; Byers, Peter; Hisama, Fuki M.; Rehm, Heidi; Nickerson, Debbie A.; Jarvik, Gail P.
Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol
AMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
2014-02-01202
OAAI
Lange, Leslie A.; Hu, Youna; Zhang, He; Xue, Chenyi; Schmidt, Ellen M.; Tang, Zheng-Zheng; Bizon, Chris; Lange, Ethan M.; Smith, Joshua D.; Turner, Emily H.; Jun, Goo; Kang, Hyun Min; Peloso, Gina; Auer, Paul; Li, Kuo-Ping; Flannick, Jason; Zhang, Ji; Fuchsberger, Christian; Gaulton, Kyle; Lindgren, Cecilia; Locke, Adam; Manning, Alisa; Sim, Xueling; Rivas, Manuel A.; Holmen, Oddgeir L.; Gottesman, Omri; Lu, Yingchang; Ruderfer, Douglas; Stah, Eli A.; Duan, Qing; Li, Yun; Durda, Peter; Jiao, Shuo; Isaacs, Aaron; Hofman, Albert; Bis, Joshua C.; Correa, Adolfo; Griswold, Michael E.; Jakobsdottir, Johanna; Smith, Albert V.; Schreiner, Pamela J.; Feitosa, Mary E.; Zhang, Qunyuan; Huffman, Jennifer E.; Crosby, Jacy; Wasse, Christina L.; Do, Ron; Franceschini, Nora; Martin, Lisa W.; Robinson, Jennifer G.; Assimes, Themistocles L.; Crosslin, David R.; Rosenthal, Elisabeth A.; Tsai, Michael; Rieder, Mark J.; Farlow, Deborah N.; Folsom, Aaron R.; Lumley, Thomas; Fox, Ervin R.; Carlson, Christopher S.; Peters, Ulrike; Jackson, Rebecca D.; Van Duijn, Cornelia M.; Uitterlinden, Andre G.; Levy, Daniel; Rotter, Jerome I.; Taylor, Herman A.; Gudnason, Vilmundur, Jr.; Siscovick, David S.; Fornage, Myriam; Borecki, Ingrid B.; Hayward, Caroline; Rudan, Igor; Chen, Y. Eugene; Bottinger, Erwin P.; Loos, Ruth J. F.; Strom, Pal; Hveem, Kristian; Boehnke, Michael; Groop, Leif; McCarthy, Mark; Meitinger, Thomas; Ballantyne, Christie M.; Gabriel, Stacey B.; O'Donne, Christopher J.; Post, Wendy S.; North, Kari E.; Reiner, Alexander P.; Boerwinkle, Eric; Psaty, Bruce M.; Altshuler, David; Kathiresan, Sekar; Lin, Dan-Yu; Jarvik, Gail P.; Cupples, L. Adrienne; Kooperberg, Charles; Wilson, James G.; Nickerson, Deborah A.; Abecasis, Goncalo R.; Rich, Stephen S.; Tracy, Russell P.; Willer, Cristen J.
Mutations in SPAG1 Cause Primary Ciliary Dyskinesia Associated with Defective Outer and Inner Dynein Arms
AMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
2013-10-01120
OAAI
Knowles, Michael R.; Ostrowski, Lawrence E.; Loges, Niki T.; Hurd, Toby; Leigh, Margaret W.; Huang, Lu; Wolf, Whitney E.; Carson, Johnny L.; Hazucha, Milan J.; Yin, Weining; Davis, Stephanie D.; Dell, Sharon D.; Ferkol, Thomas W.; Sagel, Scott D.; Olivier, Kenneth N.; Jahnke, Charlotte; Olbrich, Heike; Werner, Claudius; Raidt, Johanna; Wallmeier, Julia; Pennekamp, Petra; Dougherty, Gerard W.; Hjeij, Rim; Gee, Heon Yung; Otto, Edgar A.; Halbritter, Jan; Chaki, Moumita; Diaz, Katrina A.; Braun, Daniela A.; Porath, Jonathan D.; Schueler, Markus; Baktai, Gyoergy; Griese, Matthias; Turner, Emily H.; Lewis, Alexandra P.; Bamshad, Michael J.; Nickerson, Deborah A.; Hildebrandt, Friedhelm; Shendure, Jay; Omran, Heymut; Zariwala, Maimoona A.
Actionable, Pathogenic Incidental Findings in 1,000 Participants' Exomes
AMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
2013-10-01330
OAAI
Dorschner, Michael O.; Amendola, Laura M.; Turner, Emily H.; Robertson, Peggy D.; Shirts, Brian H.; Gallego, Carlos J.; Bennett, Robin L.; Jones, Kelly L.; Tokita, Mari J.; Bennett, James T.; Kim, Jerry H.; Rosenthal, Elisabeth A.; Kim, Daniel S.; Tabor, Holly K.; Bamshad, Michael J.; Motulsky, Arno G.; Scott, C. Ronald; Pritchard, Colin C.; Walsh, Tom; Burke, Wylie; Raskind, Wendy H.; Byers, Peter; Hisama, Fuld M.; Nickerson, Deborah A.; Jarvik, Gail P.
Mutations in KCTD1 Cause Scalp-Ear-Nipple Syndrome
AMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
2013-04-0161
OAAI
Marneros, Alexander G.; Beck, Anita E.; Turner, Emily H.; McMillin, Margaret J.; Edwards, Matthew J.; Field, Michael; Sobreira, Nara Lygia de Macena; Perez, Ana Beatriz A.; Fortes, Jose A. R.; Lampe, Anne K.; Uzielli, Maria Luisa Giovannucci; Gordon, Christopher T.; Plessis, Ghislaine; Le Merrer, Martine; Amiel, Jeanne; Reichenberger, Ernst; Shively, Kathryn M.; Cerrato, Felecia; Labow, Brian I.; Tabor, Holly K.; Smith, Joshua D.; Shendure, Jay; Nickerson, Deborah A.; Bamshad, Michael J.
Whole-Genome Analysis Reveals that Mutations in Inositol Polyphosphate Phosphatase-like 1 Cause Opsismodysplasia
AMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
2013-01-0146
OAAI
Below, Jennifer E.; Earl, Dawn L.; Shively, Kathryn M.; McMillin, Margaret J.; Smith, Joshua D.; Turner, Emily H.; Stephan, Mark J.; Al-Gazali, Lihadh I.; Hertecant, Jozef L.; Chitayat, David; Unger, Sheila; Cohn, Daniel H.; Krakow, Deborah; Swanson, James M.; Faustman, Elaine M.; Shendure, Jay; Nickerson, Deborah A.; Bamshad, Michael J.
Exome Sequencing Identifies Mutations in CCDC114 as a Cause of Primary Ciliary Dyskinesia
AMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
2013-01-01119
OAAI
Knowles, Michael R.; Leigh, Margaret W.; Ostrowski, Lawrence E.; Huang, Lu; Carson, Johnny L.; Hazucha, Milan J.; Yin, Weining; Berg, Jonathan S.; Davis, Stephanie D.; Dell, Sharon D.; Ferkol, Thomas W.; Rosenfeld, Margaret; Sagel, Scott D.; Milla, Carlos E.; Olivier, Kenneth N.; Turner, Emily H.; Lewis, Alexandra P.; Bamshad, Michael J.; Nickerson, Deborah A.; Shendure, Jay; Zariwala, Maimoona A.
Whole-Exome Capture and Sequencing Identifies HEATR2 Mutation as a Cause of Primary Ciliary Dyskinesia
AMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
2012-10-01140
OAAI
Horani, Amjad; Druley, Todd E.; Zariwala, Maimoona A.; Pate, Anand C.; Levinson, Benjamin T.; Van Arendonk, Laura G.; Thornton, Katherine C.; Giacalone, Joe C.; Albee, Alison J.; Wilson, Kate S.; Turner, Emily H.; Nickerson, Deborah A.; Shendure, Jay; Bayly, Philip V.; Leigh, Margaret W.; Knowles, Michael R.; Brody, Steven L.; Dutcher, Susan K.; Ferkol, Thomas W.
Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome
NATURE GENETICS
IF31.8
2010-08-151.1K
OAAI
Ng, Sarah B.; Bigham, Abigail W.; Buckingham, Kati J.; Hannibal, Mark C.; McMillin, Margaret J.; Gildersleeve, Heidi I.; Beck, Anita E.; Tabor, Holly K.; Cooper, Gregory M.; Mefford, Heather C.; Lee, Choli; Turner, Emily H.; Smith, Joshua D.; Rieder, Mark J.; Yoshiura, Koh-ichiro; Matsumoto, Naomichi; Ohta, Tohru; Niikawa, Norio; Nickerson, Deborah A.; Bamshad, Michael J.; Shendure, Jay

研究方向

暂未获取到该数据
J
Jay Shendure
H 指数:167论文数:674被引数:12.3万
D
Deborah A. Nickerson
H 指数:120论文数:675被引数:10.1万
M
Michael J. Bamshad
H 指数:96论文数:552被引数:4.5万
N
Norman J. Dovic̀hi
H 指数:67论文数:403被引数:1.5万
J
Joshua D. Smith
H 指数:59论文数:296被引数:2.2万
C
Colin C. Pritchard
H 指数:60论文数:286被引数:2.3万
J
Jane A. Dickerson
H 指数:20论文数:84被引数:1,272
C
Choli Lee
H 指数:34论文数:65被引数:1.7万
H
Holly K. Tabor
H 指数:47论文数:160被引数:1.4万
P
Peter H. Byers
H 指数:91论文数:418被引数:2.9万