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Disruptions of Topological Chromatin Domains Cause Pathogenic Rewiring of Gene-Enhancer Interactions
- Lupiáñez, Darío G.
- Kraft, Katerina
- Heinrich, Verena
- Krawitz, Peter
- Brancati, Francesco
- Klopocki, Eva
- Horn, Denise
- Kayserili, Hülya
- Opitz, John M.
- Laxova, Renata
- Santos-Simarro, Fernando
- Gilbert-Dussardier, Brigitte
- Wittler, Lars
- Borschiwer, Marina
- Haas, Stefan A.
- Osterwalder, Marco
- Franke, Martin
- Timmermann, Bernd
- Hecht, Jochen
- Spielmann, Malte
- Visel, Axel
- Mundlos, Stefan
2015
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Proceedings of the National Academy of Sciences - PNAS, 2011-04, Vol.108 (16), p.6543-6548
2011
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American journal of human genetics, 2010-08, Vol.87 (2), p.282-288
2010
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American journal of medical genetics. Part A, 2007-12, Vol.143A (24), p.3016-3034
2007
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American journal of medical genetics. Part A, 2013-11, Vol.161A (11), p.2726-2733
2013
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Germline mutations in DIS3L2 cause the Perlman syndrome of overgrowth and Wilms tumor susceptibility
- ASTUTI, Dewi
- MORRIS, Mark R
- COLE, Trevor
- ESSEN, Anthonie J.van
- LINGEN, Richard A.van
- NERI, Giovanni
- OPITZ, John M
- RUMP, Patrick
- STOLTE-DIJKSTRA, Irene
- MÜLLER, Ferenc
- PRUIJN, Ger J. M
- LATIF, Farida
- COOPER, Wendy N
- MAHER, Eamonn R
- STAALS, Raymond H. J
- WAKE, Naomi C
- FEWS, Graham A
- GILL, Harmeet
- GENTLE, Dean
- SHUIB, Salwati
- RICKETTS, Christopher J
2012
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American journal of human genetics, 2011-07, Vol.89 (1), p.28-43
- Rope, Alan F.
- Wang, Kai
- Evjenth, Rune
- Xing, Jinchuan
- Johnston, Jennifer J.
- Swensen, Jeffrey J.
- Johnson, W. Evan
- Moore, Barry
- Huff, Chad D.
- Bird, Lynne M.
- Carey, John C.
- Opitz, John M.
- Stevens, Cathy A.
- Jiang, Tao
- Schank, Christa
- Fain, Heidi Deborah
- Robison, Reid
- Dalley, Brian
- Chin, Steven
- South, Sarah T.
- Pysher, Theodore J.
- Jorde, Lynn B.
- Hakonarson, Hakon
- Lillehaug, Johan R.
- Biesecker, Leslie G.
- Yandell, Mark
- Arnesen, Thomas
- Lyon, Gholson J.
2011
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American journal of human genetics, 2012-03, Vol.90 (3), p.392-404
2012
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Nature genetics, 2007-04, Vol.39 (4), p.451-453
2007
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Birth defects research, 2019-04, Vol.111 (6), p.294-311
2019
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American journal of medical genetics. Part A, 2021-05, Vol.185 (5), p.1355-1362
2021
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American journal of medical genetics. Part A, 2020-12, Vol.182 (12), p.2820-2822
2020
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Journal of human genetics, 2017-12, Vol.62 (12), p.1073-1078
2017
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American journal of medical genetics. Part C, Seminars in medical genetics, 2017-09, Vol.175 (3), p.329-340
2017
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American journal of medical genetics. Part A, 2023-02, Vol.191 (2), p.640-646
2023
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The Journal of molecular diagnostics : JMD, 2013-07, Vol.15 (4), p.466-472
2013
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American journal of medical genetics. Part A, 2018-06, Vol.176 (6), p.1285-1288
2018
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American journal of medical genetics. Part A, 2016-11, Vol.170A (11), p.2803-2829
2016
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American journal of medical genetics. Part A, 2017-05, Vol.173 (5), p.1147-1148
2017
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Fetal and pediatric pathology, 2019-01, Vol.38 (1), p.91-92
2019
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American journal of medical genetics. Part A, 2016-10, Vol.170A (10), p.2503-2522
2016
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American journal of medical genetics. Part C, Seminars in medical genetics, 2014-12, Vol.166C (4), p.387-396
2014
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American journal of medical genetics. Part A, 2016-01, Vol.170A (1), p.60-61
2016
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American journal of medical genetics. Part A, 2015-11, Vol.167A (11), p.2566-2567
2015
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American journal of medical genetics. Part A, 2015-11, Vol.167A (11), p.2516-2519
2015
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