L. J. Ozelius

Monoamine oxidase deficiency in males with an X chromosome deletion

Katherine B. Sims, Albert de la Chapelle, Reijo Norio et al. · Neuron · 1989 · 108 citations

Mendelian Disorder, Genetic Disorder, Genetics +5

REPORT on the Sixth International Workshop on Chromosome 9 held at Denver, Colorado, U.S.A., 27 October 1998

Brian P. Chadwick, Lynda J. Campbell, Cynthia L. Jackson et al. · Annals of Human Genetics · 1999 · 101 citations

High mutation rate in dopa-responsive dystonia: Detection with comprehensive <i>GCHI</i> screening

J. Hagenah, Rachel Saunders‐Pullman, Katja Hedrich et al. · Neurology · 2005 · 97 citations

Mutations in <i>DYT1</i>

Kemal Kabakci, Katja Hedrich, Joanne Leung et al. · Neurology · 2004 · 86 citations

Highly polymorphic (GT)n repeat sequence in intron II of the human MAOB gene

Christine Konradi, L. J. Ozelius, Xandra O. Breakefield · Genomics · 1992 · 48 citations

Repeat Sequence, Genetic Disorder, Human Maob Gene +9