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Institute of Medical Genetics News, Events & Publications


ZORA note on the authors' stated information

  • In the exportable list, publications with less than 30 authors are transferred 1:1 to ZORA. No author names are deleted. --> Reason: complete metadata per publication, also for further use (e.g. in Swisscovery).
  • For publications with more (>30) authors, the authors are automatically truncated to the number 30 during import. In the same step, an "et al" is created.  If this leaves out UZH authors, they were added at the end, after "et al".
  • More information: Varia | University Library Zurich | UZH
  • For the complete listing of authors in order of publication, please use the authors list at the original publication. Or alternatively use the text file at the bottom of this page.

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Pulications, listed at 31/12/2001 

Martinez M-J, Binkert F, Schinzel A, Kotzot D. No Evidence of dup(7)(p11.2p13) in Silver-Russell Syndrome Am J Med Genet 2001 99; 335-337

Schinzel A, Niedrist D. Chromosome Imbalances Associated With Epilepsy Am J Med Genet (Semin. Med. Genet.) 2001 106; 119-124

Weymann S, Yonekawa Y, Khan N, Martin E, Heppner F L, Schinzel A, Kotzot D. Severe Arterial Occlusive Disorder and Brachysyndactyly in a Boy: A Further Case of Grange Syndrome? Am J Med Genet 2001 99; 190-195

Jung HH, Hergersberg M, Kneifel S, Alkadhi H, Schiess R, Weigell-Weber M, Daniels G, Kollias S, Hess K. McLeod Syndrome: A Novel Mutation, Predominant Psy-chiatric Manifestations, and Distinct Striatal Imaging Findings Ann Neurol 2001 49; 384-392

Schmidt H, Rudolph G, Hergersberg M, Schneider K, Moradi S, Meitinger T. Retinal detachment and cataract, facial dysmorphism, generalized osteoporosis, immobile spine and platyspondyly in a consanguinous kindred - a possible new syndrome Clin Genet 2001 59; 99-105

Dorn T, Riegel M, Schinzel A, Siegel AM, Krämer G. Epilepsy and trisomy 19q - different seizure patterns in a brother and a sister Epilepsy Res 2001 47; 119-126

Baumer A, Wiedemann U, Hergersberg M, Schinzel A. A novel MSP/DHPLC method für the investigation of the methylation status of imprinted genes enables the molecular detection of low cell mosaicisms Human Mutation 2001 17; 423-430

Riegel M, Morava E, Czako M, Kosztolanyi G, Schinzel A. Distal Deletion, del(2)(q33.3q33.3), in a Patient With Severe Growth Deficiency and Minor Anomalies Am J Med Genet 2001 102; 227-230

Courtens W, Vroman S, Vandenhove J, Wiedemann U, Schinzel A. Pre- and perinatal findings in partial trisomy 7q resulting from balanced parental translocations t(7;21) and t(4;7) Prenat Diagn 2001 21; 642-648

Riegel M, Baumer A, Jamar M, Delbecque K, Herens C, Verloes A, Schinzel A. Submicroscopic terminal deletions and duplications in retarded patients with unclassified malformation syndromes Hum Genet 2001 109; 286-294

Röthlisberger B, Zerova TE, Kotzot D, Buzhievskaya TI, Balmer D, Schinzel A. Supernumerary marker chromosome (1) of paternal origin and maternal uniparental disomy 1 in a developmentally delayed child J Med Genet 2001 38; 885-888

Kotzot D, Röthlisberger B, Riegel M, Schinzel A. Maternal uniparental isodisomy 11q13-->qter in a dysmorphic and mentally retarded female with partial trisomy mosaicism 11q13-->qter J Med Genet 2001 38; 876-881

Riegel M, Baumer A, Piram A, Ortolan D, Peres LC, Pina-Neto JM. De novo unbalan-ced t(11q;21q) leading to a partial monosomy 21pter-q22.2 and 11q24-qter in a patient initially diagnosed as monosomy 21 Genet Couns 2001 12; 69-75

Fokstuen S, Vrticka K, Riegel M, Da Silva V, Baumer A, Schinzel A. Velofacial hypoplasia (Sedlackova syndrome): a variant of velocardiofacial (Shprintzen) syndrome and part of the phenotypical spectrum of del 22q11.2 Eur J Pediatr 2001 160; 54-57

Wirth J, Back E, Hüttenhofer A, Northwang H-G, Lich C, Gross S, Menzel C, Schinzel A, Kioschis P, Tommerup N, Ropers H-H, Horsthemke B, Buiting K. A translocation breakpoint cluster disrupts the newly defined 3' end of the SNURF-SNRPN transcription unit on chromosome 15 Hum Mol Genet 2001 10; 201-210

Bruder CEG, Hirvelä C, Tapia-Paez I, Fransson I, Segraves R, Hamilton G, Zhang XX, Gareth Evans D, Wallace AJ, Baser ME, Zucman-Rossi J, Hergersberg M, Boltshauser E, Papi L, Rouleau GA, Poptodorov G, Jordanova A, Rask-Andersen H, Kluwe L, Mautner V, Markku S, Hung G, Mathiesen T, Möller C, Pulst SM, Harder H, Heiberg A, Honda M, MIchihito N, Sahlén S, Blennow E, Albertson DG, Pinkel D, Dumanski JP. High resolution deletion analysis of constitutional DNA from neuro-fibromatosis type 2 (NF2) patients using microarray-CGH Hum Mol Genet 2001 10; 271-282

Mikelsaar RV, Varb K, Süvari A, Schinzel A. Mosaic terminal del(19)(q13.33:) in a girl with seizures and mental retardation J Med Genet 2001 38; e2

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