Jadranka Sertić

ZMYND10 Is Mutated in Primary Ciliary Dyskinesia and Interacts with LRRC6

Maimoona A. Zariwala, Heon Yung Gee, Małgorzata Kurkowiak et al. · The American Journal of Human Genetics · 2013 · 201 citations · Full text

Pathology, Neuropathology, Medicine +4

Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: a cystic fibrosis mutation of Slavic origin common in Central and East Europe

Thilo Dörk, Milan Maçek, Frauke Mekus et al. · Human Genetics · 2000 · 145 citations

Fibrosis, Mendelian Disorder, Genetic Disorder +11

Sequential targeted exome sequencing of 1001 patients affected by unexplained limb-girdle weakness

Ana Töpf, Katherine Johnson, Adam Bates et al. · Genetics in Medicine · 2020 · 105 citations · Full text

Harpers Illustrated Biochemistry

Autori prijevoda Nicoletta Burger, Ivančica Delaš, Robert Domitrović et al. · 2011 · 95 citations

Chemical Pathology, Bioanalysis, Biochemistry

Associations between MDR1 gene polymorphisms and schizophrenia and therapeutic response to olanzapine in female schizophrenic patients

Nada Božina, Martina Rojnić Kuzman, Vesna Medved et al. · Journal of Psychiatric Research · 2006 · 84 citations

Psychiatry, Female Schizophrenic Patients, Medicine +14