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Search Results - Nissen, Anke M
Search Results - Nissen, Anke M
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Identification of genetic variants for clinical management of familial colorectal tumors
by
Dominguez-Valentin, Mev
,
Nakken, Sigve
,
Tubeuf, Hélène
,
Vodak, Daniel
,
Ekstrøm, Per Olaf
,
Nissen, Anke M
,
Morak, Monika
,
Holinski-Feder, Elke
,
Martins, Alexandra
,
Møller, Pål
,
Hovig, Eivind
Published in
BMC medical genetics
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Genetic variants of prospectively demonstrated phenocopies in BRCA1/2 kindreds
by
Dominguez-Valentin, Mev
,
Evans, D Gareth R
,
Nakken, Sigve
,
Tubeuf, Hélène
,
Vodak, Daniel
,
Ekstrøm, Per Olaf
,
Nissen, Anke M
,
Morak, Monika
,
Holinski-Feder, Elke
,
Martins, Alexandra
,
Møller, Pål
,
Hovig, Eivind
Published in
Hereditary cancer in clinical practice
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Results of multigene panel testing in familial cancer cases without genetic cause demonstrated by single gene testing
by
Dominguez-Valentin, Mev
,
Nakken, Sigve
,
Tubeuf, Hélène
,
Vodak, Daniel
,
Ekstrøm, Per Olaf
,
Nissen, Anke M.
,
Morak, Monika
,
Holinski-Feder, Elke
,
Holth, Arild
,
Capella, Gabriel
,
Davidson, Ben
,
Evans, D. Gareth
,
Martins, Alexandra
,
Møller, Pål
,
Hovig, Eivind
Published in
Scientific reports
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Potentially pathogenic germline CHEK2 c.319+2T>A among multiple early-onset cancer families
by
Dominguez-Valentin, Mev
,
Nakken, Sigve
,
Tubeuf, Hélène
,
Vodak, Daniel
,
Ekstrøm, Per Olaf
,
Nissen, Anke M.
,
Morak, Monika
,
Holinski-Feder, Elke
,
Martins, Alexandra
,
Møller, Pål
,
Hovig, Eivind
Published in
Familial cancer
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Loss of MSH2 and MSH6 due to heterozygous germline defects in MSH3 and MSH6
by
Morak, Monika
,
Käsbauer, Sarah
,
Kerscher, Martina
,
Laner, Andreas
,
Nissen, Anke M.
,
Benet-Pagès, Anna
,
Schackert, Hans K.
,
Keller, Gisela
,
Massdorf, Trisari
,
Holinski-Feder, Elke
Published in
Familial cancer
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Genome-Wide Association Study Meta-Analysis of 9619 Cases With Tic Disorders
by
Strom, Nora I.
,
Halvorsen, Matthew W.
,
Grove, Jakob
,
Ásbjörnsdóttir, Bergrún
,
Thorarensen, Ólafur
,
de Schipper, Elles
,
Bäckmann, Julia
,
Tian, Chao
,
Sul, Jae Hoon
,
Tsetsos, Fotis
,
Zelaya, Ivette
,
Osiecki, Lisa
,
Darrow, Sabrina M.
,
Hirschtritt, Matthew E.
,
Greenberg, Erica
,
Stuhrmann, Manfred
,
Dion, Yves
,
Rouleau, Guy
,
Aschauer, Harald
,
Stamenkovic, Mara
,
Schlögelhofer, Monika
,
Barr, Cathy L.
,
Grados, Marco
,
Hinney, Anke
,
King, Robert A.
,
Fernandez, Thomas V.
,
Barta, Csaba
,
Tarnok, Zsanett
,
Nagy, Peter
,
Depienne, Christel
,
Worbe, Yulia
,
Hartmann, Andreas
,
Budman, Cathy L.
,
Lyon, Gholson J.
,
McMahon, William M.
,
Batterson, James R.
,
Malaty, Irene A.
,
Okun, Michael S.
,
Berlin, Cheston
,
Woods, Douglas W.
,
Lee, Paul C.
,
Jankovic, Joseph
,
Robertson, Mary M.
,
Gilbert, Donald L.
,
Brown, Lawrence W.
,
Coffey, Barbara J.
,
Hoekstra, Pieter J.
,
Zinner, Samuel H.
,
Luðvigsson, Pétur
,
Thorarensen, Ólafur
,
Atzmon, Gil
,
Barzilai, Nir
,
Moessner, Rainald
,
Ophoff, Roel
,
Pato, Carlos N.
,
Knowles, James A.
,
Buckner, Randy L.
,
Willsey, Jeremy A.
,
Tischfield, Jay A.
,
Heiman, Gary A.
,
Stefansson, Hreinn
,
Stefansson, Kári
,
Posthuma, Danielle
,
Pauls, David L.
,
Freimer, Nelson B.
,
Davis, Lea K.
,
Paschou, Peristera
,
Coppola, Giovanni
,
Mathews, Carol A.
,
Scharf, Jeremiah M.
,
Agee, Michelle
,
Auton, Adam
,
Elson, Sarah L.
,
Furlotte, Nicholas A.
,
Hicks, Barry
,
Jewett, Ethan M.
,
Jiang, Yunxuan
,
Kleinman, Aaron
,
Lin, Keng-Han
,
Litterman, Nadia K.
,
McIntyre, Matthew H.
,
McManus, Kimberly F.
,
Mountain, Joanna L.
,
Pitts, Steven J.
,
Poznik, G. David
,
Sathirapongsasuti, J. Fah
,
Shelton, Janie F.
,
Shringarpure, Suyash
,
Tung, Joyce Y.
,
Wang, Xin
,
Als, Thomas Damm
,
Meier, Sandra M.
,
Bybjerg-Grauholm, Jonas
,
Hougaard, David M.
,
Werge, Thomas
,
Børglum, Anders D.
,
Hinds, David A.
,
Rück, Christian
,
Mataix-Cols, David
,
Mattheisen, Manuel
Published in
Biological psychiatry (1969)
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Mutations in CRADD Result in Reduced Caspase-2-Mediated Neuronal Apoptosis and Cause Megalencephaly with a Rare Lissencephaly Variant
by
Di Donato, Nataliya
,
Jean, Ying Y.
,
Maga, A. Murat
,
Krewson, Briana D.
,
Shupp, Alison B.
,
Avrutsky, Maria I.
,
Roy, Achira
,
Collins, Sarah
,
Olds, Carissa
,
Willert, Rebecca A.
,
Czaja, Agnieszka M.
,
Johnson, Rachel
,
Stover, Jessi A.
,
Gottlieb, Steven
,
Bartholdi, Deborah
,
Rauch, Anita
,
Goldstein, Amy
,
Boyd-Kyle, Victoria
,
Aldinger, Kimberly A.
,
Mirzaa, Ghayda M.
,
Nissen, Anke
,
Brigatti, Karlla W.
,
Puffenberger, Erik G.
,
Millen, Kathleen J.
,
Strauss, Kevin A.
,
Dobyns, William B.
,
Troy, Carol M.
,
Jinks, Robert N.
Published in
American journal of human genetics
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Polygenic risk score-based phenome-wide association study identifies novel associations for Tourette syndrome
by
Jain, Pritesh
,
Miller-Fleming, Tyne
,
Topaloudi, Apostolia
,
Yu, Dongmei
,
Drineas, Petros
,
Georgitsi, Marianthi
,
Yang, Zhiyu
,
Rizzo, Renata
,
Müller-Vahl, Kirsten R.
,
Tumer, Zeynep
,
Mol Debes, Nanette
,
Hartmann, Andreas
,
Depienne, Christel
,
Worbe, Yulia
,
Mir, Pablo
,
Cath, Danielle C.
,
Boomsma, Dorret I.
,
Roessner, Veit
,
Wolanczyk, Tomasz
,
Janik, Piotr
,
Szejko, Natalia
,
Zekanowski, Cezary
,
Barta, Csaba
,
Nemoda, Zsofia
,
Tarnok, Zsanett
,
Buxbaum, Joseph D.
,
Grice, Dorothy
,
Glennon, Jeffrey
,
Stefansson, Hreinn
,
Hengerer, Bastian
,
Benaroya-Milshtein, Noa
,
Cardona, Francesco
,
Hedderly, Tammy
,
Heyman, Isobel
,
Huyser, Chaim
,
Morer, Astrid
,
Mueller, Norbert
,
Munchau, Alexander
,
Plessen, Kerstin J.
,
Porcelli, Cesare
,
Walitza, Susanne
,
Schrag, Anette
,
Martino, Davide
,
Dietrich, Andrea
,
Mathews, Carol A.
,
Scharf, Jeremiah M.
,
Hoekstra, Pieter J.
,
Davis, Lea K.
,
Paschou, Peristera
Published in
Translational psychiatry
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