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Papers authored by Kuechler A

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Nicolaides-Baraitser syndrome: Delineation of the phenotype.

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Sousa SB, Abdul-Rahman OA, Bottani A, Cormier-Daire V, Fryer A, Gillessen-Kaesbach G, Horn D, Josifova D, Kuechler A, Lees M, MacDermot K, Magee A, Morice-Picard F, Rosser E, Sarkar A, Shannon N,

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American journal of medical genetics. Part A 149A(8):1628-40, 2009 Aug - Who cited this? | PubMed ID: 19606471 | Fulltext

A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader-Willi syndrome.

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Kanber D, Giltay J, Wieczorek D, Zogel C, Hochstenbach R, Caliebe A, Kuechler A, Horsthemke B, and Buiting K

European journal of human genetics : EJHG 17(5):582-90, 2009 May - Who cited this? | PubMed ID: 19066619 | Fulltext

Microcephaly, microtia, preauricular tags, choanal atresia and developmental delay in three unrelated patients: a mandibulofacial dysostosis distinct from Treacher Collins syndrome.

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Wieczorek D, Gener B, González MJ, Seland S, Fischer S, Hehr U, Kuechler A, Hoefsloot LH, de Leeuw N, Gillessen-Kaesbach G, and Lohmann DR

American journal of medical genetics. Part A 149A(5):837-43, 2009 May - Who cited this? | PubMed ID: 19334086 | Fulltext

Refining the phenotype of alpha-1a Tubulin (TUBA1A) mutation in patients with classical lissencephaly.

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Morris-Rosendahl Dj, Najm J, Lachmeijer A, Sztriha L, Martins M, Kuechler A, Haug V, Zeschnigk C, Martin P, Santos M, Vasconcelos C, Omran H, Kraus U, Van der Knaap M, Schuierer G, Kutsche K,

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Clinical genetics 74(5):425-33, 2008 Nov - Who cited this? | PubMed ID: 18954413 | Fulltext

Corrigendum: Mutations of CASK cause an X-linked brain malformation phenotype with microcephaly and hypoplasia of the brainstem and cerebellum.

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Najm J, Horn D, Wimplinger I, Golden JA, Chizhikov VV, Sudi J, Christian SL, Ullmann R, Kuechler A, Haas CA, Flubacher A, Charnas LR, Uyanik G, Frank U, Klopocki E, Dobyns WB,

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Nature genetics 40(11):1384, 2008 Nov - Who cited this? | PubMed ID: 18957986 | Fulltext

Mutations of CASK cause an X-linked brain malformation phenotype with microcephaly and hypoplasia of the brainstem and cerebellum.

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Najm J, Horn D, Wimplinger I, Golden JA, Chizhikov VV, Sudi J, Christian SL, Ullmann R, Kuechler A, Haas CA, Flubacher A, Charnas LR, Uyanik G, Frank U, Klopocki E, Dobyns WB,

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Nature genetics 40(9):1065-7, 2008 Sep - Who cited this? | PubMed ID: 19165920 | Fulltext

New immortalized cell lines of patients with small supernumerary marker chromosome: towards the establishment of a cell bank.

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Tönnies H, Pietrzak J, Bocian E, MacDermont K, Kuechler A, Belitz B, Trautmann U, Schmidt A, Schulze B, Rodríguez L, Binkert F, Yardin C, Kosyakova N, Volleth M, Mkrtchyan H, Schreyer I,

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The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 55(6):651-60, 2007 Jun - Who cited this? | PubMed ID: 17341473 | Fulltext

The presence of depression and anxiety in Parkinson's disease.

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Mercury MG, Tschan W, Kehoe R, and Kuechler A

Disease-a-month : DM 53(5):296-301, 2007 May - Who cited this? | PubMed ID: 17656191 | Fulltext

Comet fluorescence in situ hybridization analysis for oxidative stress-induced DNA damage in colon cancer relevant genes.

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Glei M, Schaeferhenrich A, Claussen U, Kuechler A, Liehr T, Weise A, Marian B, Sendt W, and Pool-Zobel BL

Toxicological sciences : an official journal of the Society of Toxicology 96(2):279, 2007 Apr - Who cited this? | PubMed ID: 17192441 | Fulltext

Neocentric small supernumerary marker chromosomes (sSMC)--three more cases and review of the literature.

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Liehr T, Utine GE, Trautmann U, Rauch A, Kuechler A, Pietracz J, Bocian E, Kosyakova N, Mrasek K, Boduroglu K, Weise A, and Aktas D

Cytogenetic and genome research 118(1):31-7, 2007 - Who cited this? | PubMed ID: 17901697 | Fulltext

Is there a higher incidence of maternal uniparental disomy 14 [upd(14)mat]? Detection of 10 new patients by methylation-specific PCR.

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Mitter D, Buiting K, Von Eggeling F, Kuechler A, Liehr T, Mau-Holzmann UA, Prott EC, Wieczorek D, and Gillessen-Kaesbach G

American journal of medical genetics. Part A 140(19):2039, 2006 Oct 1 - Who cited this? | PubMed ID: 16906536 | Fulltext

Minimal phenotype in a girl with trisomy 15q due to t(X;15)(q22.3;q11.2) translocation.

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Stankiewicz P, Kuechler A, Eller CD, Sahoo T, Baldermann C, Lieser U, Hesse M, Gläser C, Hagemann M, Yatsenko SA, Liehr T, Horsthemke B, Claussen U, Marahrens Y, Lupski JR, and Hansmann I

American journal of medical genetics. Part A 140(5):442, 2006 Mar 1 - Who cited this? | PubMed ID: 16470732 | Fulltext

FISH banding in tumor cytogenetics.

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Liehr T, Gross M, Karst C, Glaser M, Mrasek K, Starke H, Weise A, Mkrtchyan H, and Kuechler A

Cancer genetics and cytogenetics 164(1):88-9, 2006 Jan 1 - Who cited this? | PubMed ID: 16364770 | Fulltext

Multicolor fluorescence in situ hybridization (FISH) applied to FISH-banding.

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Liehr T, Starke H, Heller A, Kosyakova N, Mrasek K, Gross M, Karst C, Steinhaeuser U, Hunstig F, Fickelscher I, Kuechler A, Trifonov V, Romanenko SA, and Weise A

Cytogenetic and genome research 114(3-4):240-4, 2006 - Who cited this? | PubMed ID: 16954660 | Fulltext

A highly complex chromosomal rearrangement between five chromosomes in a healthy female diagnosed in preparation for intracytoplasmatic sperm injection.

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Kuechler A, Ziegler M, Blank C, Rommel B, Bullerdiek J, Ahrens J, Claussen U, and Liehr T

The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 53(3):355-7, 2005 Mar - Who cited this? | PubMed ID: 15750018 | Fulltext

Cytogenetic instability in young patients with multiple primary cancers.

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Keller U, Grabenbauer G, Kuechler A, Sprung CN, Müller E, Sauer R, and Distel L

Cancer genetics and cytogenetics 157(1):25-32, 2005 Feb - Who cited this? | PubMed ID: 15676143 | Fulltext

Technical report. Radiation sensitivity testing by fluorescence in-situ hybridization: how many metaphases have to be analysed?.

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Keller U, Grabenbauer G, Kuechler A, Sauer R, and Distel L

International journal of radiation biology 80(8):615-20, 2004 Aug - Who cited this? | PubMed ID: 15370973 | Fulltext

Impact of various parameters in detecting chromosomal aberrations by FISH to describe radiosensitivity.

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Keller U, Kuechler A, Liehr T, Müller E, Grabenbauer G, Sauer R, and Distel L

Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al] 180(5):289-96, 2004 May - Who cited this? | PubMed ID: 15127159 | Fulltext

Rapid detection of subtelomeric deletion/duplication by novel real-time quantitative PCR using SYBR-green dye.

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Boehm D, Herold S, Kuechler A, Liehr T, and Laccone F

Human mutation 23(4):368-78, 2004 Apr - Who cited this? | PubMed ID: 15024731 | Fulltext

The hierarchically organized splitting of chromosome bands into sub-bands analyzed by multicolor banding (MCB).

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Lehrer H, Weise A, Michel S, Starke H, Mrasek K, Heller A, Kuechler A, Claussen U, and Liehr T

Cytogenetic and genome research 105(1):25-8, 2004 - Who cited this? | PubMed ID: 15218254 | Fulltext

Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classification.

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Starke H, Nietzel A, Weise A, Heller A, Mrasek K, Belitz B, Kelbova C, Volleth M, Albrecht B, Mitulla B, Trappe R, Bartels I, Adolph S, Dufke A, Singer S, Stumm M,

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Human genetics 114(1):51-67, 2003 Dec - Who cited this? | PubMed ID: 13680362 | Fulltext

Conspicuous GTG-banding results of the centromere-near region can be caused by alphoid DNA heteromorphism.

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Liehr T, Ziegler M, Starke H, Heller A, Kuechler A, Kittner G, Beensen V, Seidel J, Hässler H, Müsebeck J, and Claussen U

Clinical genetics 64(2):166-7, 2003 Aug - Who cited this? | PubMed ID: 12859415 | Fulltext

Residual chromosomal damage after radiochemotherapy with and without amifostine detected by 24-color FISH.

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Kuechler A, Dreidax M, Pigorsch SU, Liehr T, Claussen U, Wendt TG, and Dunst J

Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al] 179(7):493-8, 2003 Jul - Who cited this? | PubMed ID: 12835887 | Fulltext

Human adenoma cells are highly susceptible to the genotoxic action of 4-hydroxy-2-nonenal.

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Schaeferhenrich A, Beyer-Sehlmeyer G, Festag G, Kuechler A, Haag N, Weise A, Liehr T, Claussen U, Marian B, Sendt W, Scheele J, and Pool-Zobel BL

Mutation research 526(1-2):19-32, 2003 May 15 - Who cited this? | PubMed ID: 12714179 | Fulltext

Putative colon cancer risk factors damage global DNA and TP53 in primary human colon cells isolated from surgical samples.

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Schaeferhenrich A, Sendt W, Scheele J, Kuechler A, Liehr T, Claussen U, Rapp A, Greulich KO, and Pool-Zobel BL

Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association 41(5):655-64, 2003 May - Who cited this? | PubMed ID: 12659718 | Fulltext

Precise breakpoint characterization of the colon adenocarcinoma cell line HT-29 clone 19A by means of 24-color fluorescence in situ hybridization and multicolor banding.

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Kuechler A, Weise A, Michel S, Schaeferhenrich A, Pool-Zobel BL, Claussen U, and Liehr T

Genes, chromosomes & cancer 36(2):207-10, 2003 Feb - Who cited this? | PubMed ID: 12508250 | Fulltext

Multitude multicolor chromosome banding (mMCB) - a comprehensive one-step multicolor FISH banding method.

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Weise A, Heller A, Starke H, Mrasek K, Kuechler A, Pool-Zobel BL, Claussen U, and Liehr T

Cytogenetic and genome research 103(1-2):34-9, 2003 - Who cited this? | PubMed ID: 15004461 | Fulltext

Microdissection based high resolution multicolor banding for all 24 human chromosomes.

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Liehr T, Heller A, Starke H, Rubtsov N, Trifonov V, Mrasek K, Weise A, Kuechler A, and Claussen U

International journal of molecular medicine 9(4):335-9, 2002 Apr - Who cited this? | PubMed ID: 11891523 | Fulltext

Is 24-color FISH detection of in-vitro radiation-induced chromosomal aberrations suited to determine individual intrinsic radiosensitivity?.

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Kuechler A, Neubauer S, Grabenbauer GG, Claussen U, Liehr T, Sauer R, and Wendt TG

Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al] 178(4):209-15, 2002 Apr - Who cited this? | PubMed ID: 12040758 | Fulltext

Multicolor chromosome banding (MCB) with YAC/BAC-based probes and region-specific microdissection DNA libraries.

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Liehr T, Weise A, Heller A, Starke H, Mrasek K, Kuechler A, Weier HU, and Claussen U

Cytogenetic and genome research 97(1-2):43-50, 2002 - Who cited this? | PubMed ID: 12438737 | Fulltext

Comparative M-FISH and CGH analyses in sensitive and drug-resistant human T-cell acute leukemia cell lines.

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Weise A, Liehr T, Efferth T, Kuechler A, and Gebhart E

Cytogenetic and genome research 98(2-3):118-25, 2002 - Who cited this? | PubMed ID: 12697993 | Fulltext

Detection of microdeletions in the short arm of the X chromosome by chromosome stretching.

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Kuechler A, Mueller CR, Liehr T, and Claussen U

Cytogenetics and cell genetics 95(1-2):12-6, 2001 - Who cited this? | PubMed ID: 11978963 | Fulltext

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