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Search Results - Golden, Denae M.
Search Results - Golden, Denae M.
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Deletion 17q12 Is a Recurrent Copy Number Variant that Confers High Risk of Autism and Schizophrenia
by
Moreno-De-Luca, Daniel
,
Mulle, Jennifer G.
,
Kaminsky, Erin B.
,
Sanders, Stephan J.
,
Myers, Scott M.
,
Adam, Margaret P.
,
Pakula, Amy T.
,
Eisenhauer, Nancy J.
,
Uhas, Kim
,
Weik, LuAnn
,
Guy, Lisa
,
Care, Melanie E.
,
Morel, Chantal F.
,
Boni, Charlotte
,
Salbert, Bonnie Anne
,
Chandrareddy, Ashadeep
,
Demmer, Laurie A.
,
Chow, Eva W.C.
,
Surti, Urvashi
,
Aradhya, Swaroop
,
Pickering, Diane L.
,
Golden, Denae M.
,
Sanger, Warren G.
,
Aston, Emily
,
Brothman, Arthur R.
,
Gliem, Troy J.
,
Thorland, Erik C.
,
Ackley, Todd
,
Iyer, Ram
,
Huang, Shuwen
,
Barber, John C.
,
Crolla, John A.
,
Warren, Stephen T.
,
Martin, Christa L.
,
Ledbetter, David H.
Published in
American journal of human genetics
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Copy number variant discrepancy resolution using the ClinGen dosage sensitivity map results in updated clinical interpretations in ClinVar
by
Riggs, Erin R.
,
Nelson, Tristan
,
Merz, Andrew
,
Ackley, Todd
,
Bunke, Brian
,
Collins, Christin D.
,
Collinson, Morag N.
,
Fan, Yao‐Shan
,
Goodenberger, McKinsey L.
,
Golden, Denae M.
,
Haglund‐Hazy, Linda
,
Krgovic, Danijela
,
Lamb, Allen N.
,
Lewis, Zoe
,
Li, Guang
,
Liu, Yajuan
,
Meck, Jeanne
,
Neufeld‐Kaiser, Whitney
,
Runke, Cassandra K.
,
Sanmann, Jennifer N.
,
Stavropoulos, Dimitri J.
,
Strong, Emma
,
Su, Meng
,
Tayeh, Marwan K.
,
Kokalj Vokac, Nadja
,
Thorland, Erik C.
,
Andersen, Erica
,
Martin, Christa L.
Published in
Human mutation
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Reprogramming of ovarian granulosa cells by YAP1 leads to development of high-grade cancer with mesenchymal lineage and serous features
by
Lv, Xiangmin
,
He, Chunbo
,
Huang, Cong
,
Hua, Guohua
,
Chen, Xingcheng
,
Timm, Barbara K.
,
Maclin, Victoria M.
,
Haggerty, Abigail A.
,
Aust, Shelly K.
,
Golden, Denae M.
,
Dave, Bhavana J.
,
Tseng, Yun-An
,
Chen, Li
,
Wang, Hongbo
,
Chen, Peichao
,
Klinkebiel, David L.
,
Karpf, Adam R.
,
Dong, Jixin
,
Drapkin, Ronny I.
,
Rueda, Bo R.
,
Davis, John S.
,
Wang, Cheng
Published in
Science bulletin (Beijing)
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Assessing the utility of confirmatory studies following identification of large-scale genomic imbalances by microarray
by
Sanmann, Jennifer N
,
Pickering, Diane L
,
Golden, Denae M
,
Stevens, Jadd M
,
Hempel, Thomas E
,
Althof, Pamela A
,
Wiggins, Michele L
,
Starr, Lois J
,
Davé, Bhavana J
,
Sanger, Warren G
Published in
Genetics in medicine
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An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities
by
Kaminsky, Erin B
,
Kaul, Vineith
,
Paschall, Justin
,
Church, Deanna M
,
Bunke, Brian
,
Kunig, Dawn
,
Moreno-De-Luca, Daniel
,
Moreno-De-Luca, Andres
,
Mulle, Jennifer G
,
Warren, Stephen T
,
Richard, Gabriele
,
Compton, John G
,
Fuller, Amy E
,
Gliem, Troy J
,
Huang, Shuwen
,
Collinson, Morag N
,
Beal, Sarah J
,
Ackley, Todd
,
Pickering, Diane L
,
Golden, Denae M
,
Aston, Emily
,
Whitby, Heidi
,
Shetty, Shashirekha
,
Rossi, Michael R
,
Rudd, M Katharine
,
South, Sarah T
,
Brothman, Arthur R
,
Sanger, Warren G
,
Iyer, Ramaswamy K
,
Crolla, John A
,
Thorland, Erik C
,
Aradhya, Swaroop
,
Ledbetter, David H
,
Martin, Christa L
Published in
Genetics in medicine
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Deletion 17q12 Is a Recurrent Copy Number Variant that Confers High Risk of Autism and Schizophrenia
by
Moreno-De-Luca, Daniel
,
Mulle, Jennifer G.
,
Kaminsky, Erin B.
,
Sanders, Stephan J.
,
Myers, Scott M.
,
Adam, Margaret P.
,
Pakula, Amy T.
,
Eisenhauer, Nancy J.
,
Uhas, Kim
,
Weik, LuAnn
,
Guy, Lisa
,
Care, Melanie E.
,
Morel, Chantal F.
,
Boni, Charlotte
,
Salbert, Bonnie Anne
,
Chandrareddy, Ashadeep
,
Demmer, Laurie A.
,
Chow, Eva W.C.
,
Surti, Urvashi
,
Aradhya, Swaroop
,
Pickering, Diane L.
,
Golden, Denae M.
,
Sanger, Warren G.
,
Aston, Emily
,
Brothman, Arthur R.
,
Gliem, Troy J.
,
Thorland, Erik C.
,
Ackley, Todd
,
Iyer, Ram
,
Huang, Shuwen
,
Barber, John C.
,
Crolla, John A.
,
Warren, Stephen T.
,
Martin, Christa L.
,
Ledbetter, David H.
Published in
American journal of human genetics
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7
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An evidence-based approach to establish the functional and clinical significance of CNVs in intellectual and developmental disabilities
by
Kaminsky, Erin B.
,
Kaul, Vineith
,
Paschall, Justin
,
Church, Deanna M.
,
Bunke, Brian
,
Kunig, Dawn
,
Moreno-De-Luca, Daniel
,
Moreno-De-Luca, Andres
,
Mulle, Jennifer G.
,
Warren, Stephen T.
,
Richard, Gabriele
,
Compton, John G.
,
Fuller, Amy E.
,
Gliem, Troy J.
,
Huang, Shuwen
,
Collinson, Morag N.
,
Beal, Sarah J.
,
Ackley, Todd
,
Pickering, Diane L.
,
Golden, Denae M.
,
Aston, Emily
,
Whitby, Heidi
,
Shetty, Shashirekha
,
Rossi, Michael R.
,
Rudd, M. Katharine
,
South, Sarah T.
,
Brothman, Arthur R.
,
Sanger, Warren G.
,
Iyer, Ramaswamy K.
,
Crolla, John A.
,
Thorland, Erik C.
,
Aradhya, Swaroop
,
Ledbetter, David H.
,
Martin, Christa L.
Published in
Genetics in medicine
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8
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Deletion 1 7q12 Is a Recurrent Copy Number Variant that Confers High Risk of Autism and Schizophrenia
by
MORENO-DE-LUCA, Daniel
,
CONSORTIUM, Sgene
,
UHAS, Kim
,
WEIK, Luann
,
GUY, Lisa
,
CARE, Melanie E
,
MOREL, Chantal F
,
BONI, Charlotte
,
SALBERT, Bonnie Anne
,
CHANDRAREDDY, Ashadeep
,
DEMMER, Laurie A
,
CHOW, Eva W. C
,
MULLE, Jennifer G
,
SURTI, Urvashi
,
ARADHYA, Swaroop
,
PICKERING, Diane L
,
GOLDEN, Denae M
,
SANDER, Warren G
,
ASTON, Emily
,
BROTHMAN, Arthur R
,
GLIEM, Troy J
,
THORLAND, Erik C
,
ACKLEY, Todd
,
KAMINSKY, Erin B
,
IYER, Ram
,
SHUWEN HUANG
,
BARBER, John C
,
CROLLA, John A
,
WARREN, Stephen T
,
MARTIN, Christa L
,
LEDBETTER, David H
,
SANDERS, Stephan J
,
STAR, Gene
,
MYERS, Scott M
,
ADAM, Margaret P
,
PAKULA, Amy T
,
EISENHAUER, Nancy J
Published in
American journal of human genetics
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Article
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