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Movement disorders, 2023-08, Vol.38 (8), p.1570-1572
2023
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Movement disorders, 2019-04, Vol.34 (4), p.584-585
2019
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Scientific reports, 2021-06, Vol.11 (1), p.12175-12175, Article 12175
2021
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Neurodegenerative disease management, 2016-08, Vol.6 (4), p.331-343
2016
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European journal of human genetics : EJHG, 2016-10, Vol.24 (10), p.1396-1402
2016
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Human molecular genetics, 2019-11, Vol.28 (21), p.3543-3551
2019
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European journal of human genetics : EJHG, 2012-01, Vol.20 (1), p.33-40
2012
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American journal of human genetics, 2010-12, Vol.87 (6), p.757-767
- Li, Yun
- Laue, Kathrin
- Temtamy, Samia
- Aglan, Mona
- Kotan, L. Damla
- Yigit, Gökhan
- Canan, Husniye
- Pawlik, Barbara
- Nürnberg, Gudrun
- Wakeling, Emma L.
- Quarrell, Oliver W.
- Baessmann, Ingelore
- Lanktree, Matthew B.
- Yilmaz, Mustafa
- Hegele, Robert A.
- Amr, Khalda
- May, Klaus W.
- Nürnberg, Peter
- Topaloglu, A. Kemal
- Hammerschmidt, Matthias
- Wollnik, Bernd
2010
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European journal of human genetics : EJHG, 2019-08, Vol.27 (8), p.1215-1224
2019
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American journal of human genetics, 2011-05, Vol.88 (5), p.523-535
- Bakircioglu, Mehmet
- Carvalho, Ofélia P.
- Khurshid, Maryam
- Cox, James J.
- Tuysuz, Beyhan
- Barak, Tanyeri
- Yilmaz, Saliha
- Caglayan, Okay
- Dincer, Alp
- Nicholas, Adeline K.
- Quarrell, Oliver
- Springell, Kelly
- Karbani, Gulshan
- Malik, Saghira
- Gannon, Caroline
- Sheridan, Eamonn
- Crosier, Moira
- Lisgo, Steve N.
- Lindsay, Susan
- Bilguvar, Kaya
- Gergely, Fanni
- Gunel, Murat
- Woods, C. Geoffrey
2011
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Genetics in medicine, 2023-01, Vol.25 (1), p.37-48
- Loong, Lucy
- Tardivo, Agostina
- Knaus, Alexej
- Hashim, Mona
- Pagnamenta, Alistair T.
- Alt, Kerstin
- Böhrer-Rabel, Helena
- Caro-Llopis, Alfonso
- Cole, Trevor
- Distelmaier, Felix
- Edery, Patrick
- Ferreira, Carlos R.
- Jezela-Stanek, Aleksandra
- Kerr, Bronwyn
- Kluger, Gerhard
- Krawitz, Peter M.
- Kuhn, Marius
- Lemke, Johannes R.
- Lesca, Gaetan
- Lynch, Sally Ann
- Martinez, Francisco
- Maxton, Caroline
- Mierzewska, Hanna
- Monfort, Sandra
- Nicolai, Joost
- Orellana, Carmen
- Pal, Deb K.
- Płoski, Rafał
- Quarrell, Oliver W.
- Rosello, Monica
- Rydzanicz, Małgorzata
- Sabir, Ataf
- Śmigiel, Robert
- Stegmann, Alexander P.A.
- Stewart, Helen
- Stumpel, Constance
- Szczepanik, Elżbieta
- Tzschach, Andreas
- Wolfe, Lynne
- Taylor, Jenny C.
- Murakami, Yoshiko
- Kinoshita, Taroh
- Bayat, Allan
- Kini, Usha
2023
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Nature genetics, 2003-04, Vol.33 (4), p.487-491
2003
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Journal of the American Heart Association, 2023-09, Vol.12 (17), p.e029100-e029100
2023
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BMJ open, 2021-09, Vol.11 (9), p.e049386-e049386
- Wolstencroft, Jeanne
- Hull, Laura
- Warner, Lauren
- Akhtar, Tooba Nadeem
- Mandy, William
- Skuse, David
- Baker, Kate
- Dewhurst, Eleanor
- Lafont, Amy
- Lucy Raymond, F
- Shirley, Terry
- Tilley, Hayley
- Timur, Husne
- Titterton, Catherine
- Walker, Neil
- Wallwork, Sarah
- Wicks, Francesca
- Ye, Zheng
- Erwood, Marie
- Andrews, Sophie
- Birch, Philippa
- Bowen, Samantha
- Bradley, Karen
- Challenger, Aimee
- Chawner, Samuel
- Cuthbert, Andrew
- Hall, Jeremy
- Holmans, Peter
- Law, Sarah
- Lewis, Nicola
- Morrison, Sinead
- Moss, Hayley
- Owen, Michael
- Ray, Sinead
- Sopp, Matthew
- Tong, Molly
- Bree, Marianne van den
- Coscini, Nadia
- Davies, Sarah
- Denaxas, Spiros
- Denyer, Hayley
- Fatih, Nasrtullah
- Juj, Manoj
- Kerry, Ellie
- Lucock, Anna
- Printzlau, Frida
- Srinivasan, Ramya
- Walker, Susan
- Watkins, Alice
- Searle, Beverly
- Pelling, Anna
- Dean, John
- Robertson, Lisa
- Alan, Denise Williams
- Lucy, Donaldson
- Procter, Annie
- Berg, Jonathan
- Lampe, Anne
- Rankin, Julia
- Joss, Shelagh
- Chitty, Lyn
- Flinter, Frances
- Holder, Muriel
- Kraus, Alison
- Barwell, Julian
- Vasudevan, Pradeep
- Weber, Astrid
- Newman, William
- Splitt, Miranda
- Clowes, Virginia
- Dijk, Fleur van
- Harrison, Rachel
- Kini, Usha
- Quarrell, Oliver
- Baralle, Diana
- Mansour, Sahar
- Crow, Yanick
2021
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Neurodegenerative Disease Management, 2013-06, Vol.3 (3), p.267-276
2013
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European journal of human genetics : EJHG, 2016-10, Vol.24 (10), p.1515-1515
2016
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Pediatric and developmental pathology, 2018-11, Vol.21 (6), p.580-584
2018
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Molecular genetics & genomic medicine, 2021-12, Vol.9 (12), p.e1685-n/a
2021
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Movement disorders clinical practice (Hoboken, N.J.), 2023-10, Vol.10 (10), p.1552-1553
2023
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Journal of medical genetics, 2007-03, Vol.44 (3), p.e68-e68
2007
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European journal of human genetics : EJHG, 2005-05, Vol.13 (5), p.556-562
2005
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American journal of medical genetics. Part B, Neuropsychiatric genetics, 2018-01, Vol.177 (1), p.35-39
- Quarrell, Oliver W.
- Clarke, Angus J.
- Compton, Cecilia
- de Die‐Smulders, Christine E.M.
- Fryer, Alan
- Jenkins, Sian
- Lahiri, Nayana
- MacLeod, Rhona
- Miedzybrodzka, Zosia
- Morrison, Patrick J.
- Musgrave, Hannah
- O'Driscoll, Mary
- Strong, Mark
- van Belzen, Martine J.
- Vermeer, Sascha
- Verschuuren‐Bemelmans, Corien C.
- Bijlsma, Emilia K.
2018
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Journal of health psychology, 2008-01, Vol.13 (1), p.5-16
2008
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European journal of human genetics : EJHG, 2006-07, Vol.14 (7), p.884-887
2006
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Human mutation, 2010-12, Vol.31 (12), p.1343-1351
2010
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