Author

Mihailo Vujic

Observed names: M Vujic, M. Vujic, Mihailo Vujic G

Institution: Sahlgrenska University Hospital

Observed institutions: Uppsala University Hospital, Sahlgrenska University Hospital, Hammersmith Hospital, Swedish University of Agricultural Sciences, Imperial College London, University of Gothenburg

OpenAlex ID: A5011156311

Identification of the gene responsible for Best macular dystrophy

1998 · Konstantin Petrukhin, Markus J. Koisti, et al. · Nature Genetics · 688

Subtelomeric rearrangements detected in patients with idiopathic mental retardation

2001 · Britt‐Marie Anderlid, Jacqueline Schoumans, et al. · American Journal of Medical Genetics · 182

Incompletely Penetrant PKD1 Alleles Mimic the Renal Manifestations of ARPKD

2010 · Mihailo Vujic, Christina M. Heyer, et al. · Journal of the American Society of Nephrology · 149

Mutations in SPINT2 Cause a Syndromic Form of Congenital Sodium Diarrhea

2009 · Peter Heinz-Erian, Thomas Müller, et al. · The American Journal of Human Genetics · 125

Swedish survey on extra structurally abnormal chromosomes in 39 105 consecutive prenatal diagnoses: Prevalence and characterization by fluorescence in situ hybridization

1994 · Elisabeth Blennow, The‐Hung Bui, et al. · Prenatal Diagnosis · 108

Multiplex Ligation-Dependent Probe Amplification (MLPA) Detects Large Deletions in the MECP2 Gene of Swedish Rett Syndrome Patients

2003 · Anna Erlandson, Lena Samuelsson, et al. · Genetic Testing · 71

Novel missense mutations in the glycine receptor β subunit gene (GLRB) in startle disease

2012 · Victoria M. James, Anna Bode, et al. · Neurobiology of Disease · 57

Maternal origin of inv dup(15) chromosomes in infantile autism

1996 · T. Martinsson, T. Johannesson, et al. · European Child & Adolescent Psychiatry · 54

Functional analysis of the novel TBX5c.1333delC mutation resulting in an extended TBX5 protein

2008 · Johann Böhm, Wolfram Heinritz, et al. · BMC Medical Genetics · 30

Localization of a gene for autosomal dominant Larsen syndrome to chromosome region 3p21.1-14.1 in the proximity of, but distinct from, the COL7A1 locus.

1995 · M Vujic, K Hallstensson, et al. · PubMed Central · 26

Antenatal diagnosis of hereditary fetal growth retardation with aminoaciduria, cholestasis, iron overload, and lactic acidosis in the newborn infant

2002 · Vineta Fellman, Ilona Visapää, et al. · Acta Obstetricia Et Gynecologica Scandinavica · 20

A case report of two male siblings with autism and duplication of Xq13–q21, a region including three genes predisposing for autism

2013 · Elisabet Wentz, Mihailo Vujic, et al. · European Child & Adolescent Psychiatry · 16

Congenital variant Rett syndrome in a girl with terminal deletion of chromosome 3p

1999 · Jan Wahlström, Anna Uller, et al. · Journal of Medical Genetics · 16

Localization of the Human Tripeptidyl Peptidase II Gene (TPP2) to 13q32-q33 by Nonradioactive in Situ Hybridization and Somatic Cell Hybrids

1993 · Tommy Martinsson, Mihailo Vujic, et al. · Genomics · 9

Hereditary multiple and isolated sporadic exostoses in the same kindred: Identification of the causative gene (EXT2) and detection of a new mutation, nt112delAT, that distinguishes the two phenotypes

2004 · Mihailo Vujic, Annika Bergman, et al. · International Journal of Molecular Medicine · 6

Localization of five human genes by clinical and molecular genetic methods

2003 · Mihailo Vujic · Gothenburg University Publications Electronic Archive (Gothenburg University)

Works count: 17

Citation count: 1,557

H-index: 13

I10-index: 13