Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by
Crossref.
Mayo, Oliver
2008.
A Century of Hardy–Weinberg Equilibrium.
Twin Research and Human Genetics,
Vol. 11,
Issue. 3,
p.
249.
Uher, R
2009.
The role of genetic variation in the causation of mental illness: an evolution-informed framework.
Molecular Psychiatry,
Vol. 14,
Issue. 12,
p.
1072.
Need, Anna C.
Ge, Dongliang
Weale, Michael E.
Maia, Jessica
Feng, Sheng
Heinzen, Erin L.
Shianna, Kevin V.
Yoon, Woohyun
Kasperavičiūtė, Dalia
Gennarelli, Massimo
Strittmatter, Warren J.
Bonvicini, Cristian
Rossi, Giuseppe
Jayathilake, Karu
Cola, Philip A.
McEvoy, Joseph P.
Keefe, Richard S. E.
Fisher, Elizabeth M. C.
St. Jean, Pamela L.
Giegling, Ina
Hartmann, Annette M.
Möller, Hans-Jürgen
Ruppert, Andreas
Fraser, Gillian
Crombie, Caroline
Middleton, Lefkos T.
St. Clair, David
Roses, Allen D.
Muglia, Pierandrea
Francks, Clyde
Rujescu, Dan
Meltzer, Herbert Y.
Goldstein, David B.
and
McCarthy, Mark I.
2009.
A Genome-Wide Investigation of SNPs and CNVs in Schizophrenia.
PLoS Genetics,
Vol. 5,
Issue. 2,
p.
e1000373.
Wallace, Helen
2010.
Quality Issues in Clinical Genetic Services.
p.
191.
Becker, Frauke
van El, Carla G
Ibarreta, Dolores
Zika, Eleni
Hogarth, Stuart
Borry, Pascal
Cambon-Thomsen, Anne
Cassiman, Jean Jacques
Evers-Kiebooms, Gerry
Hodgson, Shirley
Janssens, A Cécile J W
Kaariainen, Helena
Krawczak, Michael
Kristoffersson, Ulf
Lubinski, Jan
Patch, Christine
Penchaszadeh, Victor B
Read, Andrew
Rogowski, Wolf
Sequeiros, Jorge
Tranebjaerg, Lisbeth
van Langen, Irene M
Wallace, Helen
Zimmern, Ron
Schmidtke, Jörg
and
Cornel, Martina C
2011.
Genetic testing and common disorders in a public health framework: how to assess relevance and possibilities.
European Journal of Human Genetics,
Vol. 19,
Issue. S1,
p.
S6.
Mitchell, Kevin J
2012.
What is complex about complex disorders?.
Genome Biology,
Vol. 13,
Issue. 1,
p.
237.
Jarick, I
Volckmar, A-L
Pütter, C
Pechlivanis, S
Nguyen, T T
Dauvermann, M R
Beck, S
Albayrak, Ö
Scherag, S
Gilsbach, S
Cichon, S
Hoffmann, P
Degenhardt, F
Nöthen, M M
Schreiber, S
Wichmann, H-E
Jöckel, K-H
Heinrich, J
Tiesler, C M T
Faraone, S V
Walitza, S
Sinzig, J
Freitag, C
Meyer, J
Herpertz-Dahlmann, B
Lehmkuhl, G
Renner, T J
Warnke, A
Romanos, M
Lesch, K-P
Reif, A
Schimmelmann, B G
Hebebrand, J
Scherag, A
and
Hinney, A
2014.
Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder.
Molecular Psychiatry,
Vol. 19,
Issue. 1,
p.
115.
Mitchell, Kevin J.
2015.
The Genetics of Neurodevelopmental Disorders.
p.
1.
Sanz-Lozano, Catalina S.
García-Solaesa, Virginia
Davila, Ignacio
and
Isidoro-García, María
2016.
Molecular Genetics of Asthma.
Vol. 1434,
Issue. ,
p.
1.
Long, Yi
Su, Ying
Ai, Huashui
Zhang, Zhiyan
Yang, Bin
Ruan, Guorong
Xiao, Shijun
Liao, Xinjun
Ren, Jun
Huang, Lusheng
and
Ding, Nengshui
2016.
A genome‐wide association study of copy number variations with umbilical hernia in swine.
Animal Genetics,
Vol. 47,
Issue. 3,
p.
298.