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Items: 1 to 50 of 127

1.

Chromosome Banding in Amphibia. XXXV. Highly Mobile Nucleolus Organizing Regions in Craugastor fitzingeri (Anura, Craugastoridae).

Schmid M, Steinlein C, Feichtinger W, Nanda I.

Cytogenet Genome Res. 2017;152(4):180-193. doi: 10.1159/000481554. Epub 2017 Oct 24.

PMID:
29059674
2.

Genetics of Tinnitus: Still in its Infancy.

Vona B, Nanda I, Shehata-Dieler W, Haaf T.

Front Neurosci. 2017 May 8;11:236. doi: 10.3389/fnins.2017.00236. eCollection 2017. Review.

3.

Analysis of global DNA methylation changes in primary human fibroblasts in the early phase following X-ray irradiation.

Maierhofer A, Flunkert J, Dittrich M, Müller T, Schindler D, Nanda I, Haaf T.

PLoS One. 2017 May 10;12(5):e0177442. doi: 10.1371/journal.pone.0177442. eCollection 2017.

4.

Epigenetic signatures of gestational diabetes mellitus on cord blood methylation.

Haertle L, El Hajj N, Dittrich M, Müller T, Nanda I, Lehnen H, Haaf T.

Clin Epigenetics. 2017 Mar 27;9:28. doi: 10.1186/s13148-017-0329-3. eCollection 2017.

5.

SLC2A3 single-nucleotide polymorphism and duplication influence cognitive processing and population-specific risk for attention-deficit/hyperactivity disorder.

Merker S, Reif A, Ziegler GC, Weber H, Mayer U, Ehlis AC, Conzelmann A, Johansson S, Müller-Reible C, Nanda I, Haaf T, Ullmann R, Romanos M, Fallgatter AJ, Pauli P, Strekalova T, Jansch C, Vasquez AA, Haavik J, Ribasés M, Ramos-Quiroga JA, Buitelaar JK, Franke B, Lesch KP.

J Child Psychol Psychiatry. 2017 Jul;58(7):798-809. doi: 10.1111/jcpp.12702. Epub 2017 Feb 22.

PMID:
28224622
6.

DNA Damage Signaling Instructs Polyploid Macrophage Fate in Granulomas.

Herrtwich L, Nanda I, Evangelou K, Nikolova T, Horn V, Sagar, Erny D, Stefanowski J, Rogell L, Klein C, Gharun K, Follo M, Seidl M, Kremer B, Münke N, Senges J, Fliegauf M, Aschman T, Pfeifer D, Sarrazin S, Sieweke MH, Wagner D, Dierks C, Haaf T, Ness T, Zaiss MM, Voll RE, Deshmukh SD, Prinz M, Goldmann T, Hölscher C, Hauser AE, Lopez-Contreras AJ, Grün D, Gorgoulis V, Diefenbach A, Henneke P, Triantafyllopoulou A.

Cell. 2016 Nov 17;167(5):1264-1280.e18. doi: 10.1016/j.cell.2016.09.054. Epub 2016 Oct 27.

7.

CpG sites with continuously increasing or decreasing methylation from early to late human fetal brain development.

Schneider E, Dittrich M, Böck J, Nanda I, Müller T, Seidmann L, Tralau T, Galetzka D, El Hajj N, Haaf T.

Gene. 2016 Oct 30;592(1):110-118. doi: 10.1016/j.gene.2016.07.058. Epub 2016 Jul 25.

8.

Epigenetic dysregulation in the developing Down syndrome cortex.

El Hajj N, Dittrich M, Böck J, Kraus TF, Nanda I, Müller T, Seidmann L, Tralau T, Galetzka D, Schneider E, Haaf T.

Epigenetics. 2016 Aug 2;11(8):563-78. doi: 10.1080/15592294.2016.1192736. Epub 2016 May 31.

9.

Dynamics of vertebrate sex chromosome evolution: from equal size to giants and dwarfs.

Schartl M, Schmid M, Nanda I.

Chromosoma. 2016 Jun;125(3):553-71. doi: 10.1007/s00412-015-0569-y. Epub 2015 Dec 29. Review.

PMID:
26715206
10.

A Novel de novo Mutation in CEACAM16 Associated with Postlingual Hearing Impairment.

Hofrichter MA, Nanda I, Gräf J, Schröder J, Shehata-Dieler W, Vona B, Haaf T.

Mol Syndromol. 2015 Oct;6(4):156-63. doi: 10.1159/000439576. Epub 2015 Sep 3.

11.

Third Report on Chicken Genes and Chromosomes 2015.

Schmid M, Smith J, Burt DW, Aken BL, Antin PB, Archibald AL, Ashwell C, Blackshear PJ, Boschiero C, Brown CT, Burgess SC, Cheng HH, Chow W, Coble DJ, Cooksey A, Crooijmans RP, Damas J, Davis RV, de Koning DJ, Delany ME, Derrien T, Desta TT, Dunn IC, Dunn M, Ellegren H, Eöry L, Erb I, Farré M, Fasold M, Fleming D, Flicek P, Fowler KE, Frésard L, Froman DP, Garceau V, Gardner PP, Gheyas AA, Griffin DK, Groenen MA, Haaf T, Hanotte O, Hart A, Häsler J, Hedges SB, Hertel J, Howe K, Hubbard A, Hume DA, Kaiser P, Kedra D, Kemp SJ, Klopp C, Kniel KE, Kuo R, Lagarrigue S, Lamont SJ, Larkin DM, Lawal RA, Markland SM, McCarthy F, McCormack HA, McPherson MC, Motegi A, Muljo SA, Münsterberg A, Nag R, Nanda I, Neuberger M, Nitsche A, Notredame C, Noyes H, O'Connor R, O'Hare EA, Oler AJ, Ommeh SC, Pais H, Persia M, Pitel F, Preeyanon L, Prieto Barja P, Pritchett EM, Rhoads DD, Robinson CM, Romanov MN, Rothschild M, Roux PF, Schmidt CJ, Schneider AS, Schwartz MG, Searle SM, Skinner MA, Smith CA, Stadler PF, Steeves TE, Steinlein C, Sun L, Takata M, Ulitsky I, Wang Q, Wang Y, Warren WC, Wood JM, Wragg D, Zhou H.

Cytogenet Genome Res. 2015;145(2):78-179. doi: 10.1159/000430927. Epub 2015 Jul 14. No abstract available.

12.

DFNB16 is a frequent cause of congenital hearing impairment: implementation of STRC mutation analysis in routine diagnostics.

Vona B, Hofrichter MA, Neuner C, Schröder J, Gehrig A, Hennermann JB, Kraus F, Shehata-Dieler W, Klopocki E, Nanda I, Haaf T.

Clin Genet. 2015;87(1):49-55. doi: 10.1111/cge.12332. Epub 2014 Jan 21.

13.

Non-syndromic hearing loss gene identification: A brief history and glimpse into the future.

Vona B, Nanda I, Hofrichter MA, Shehata-Dieler W, Haaf T.

Mol Cell Probes. 2015 Oct;29(5):260-70. doi: 10.1016/j.mcp.2015.03.008. Epub 2015 Apr 3. Review.

14.

In vitro evidence for senescent multinucleated melanocytes as a source for tumor-initiating cells.

Leikam C, Hufnagel AL, Otto C, Murphy DJ, Mühling B, Kneitz S, Nanda I, Schmid M, Wagner TU, Haferkamp S, Bröcker EB, Schartl M, Meierjohann S.

Cell Death Dis. 2015 Apr 2;6:e1711. doi: 10.1038/cddis.2015.71.

15.

Co-Occurence of Reciprocal Translocation and COL2A1 Mutation in a Fetus with Severe Skeletal Dysplasia: Implications for Genetic Counseling.

Heinrich T, Nanda I, Rehn M, Zollner U, Ernestus K, Wirth C, Schlüter G, Schmid M, Kunstmann E.

Cytogenet Genome Res. 2015;145(1):25-8. doi: 10.1159/000381169. Epub 2015 Mar 25.

PMID:
25823796
16.

Terminal chromosome 4q deletion syndrome in an infant with hearing impairment and moderate syndromic features: review of literature.

Vona B, Nanda I, Neuner C, Schröder J, Kalscheuer VM, Shehata-Dieler W, Haaf T.

BMC Med Genet. 2014 Jun 25;15:72. doi: 10.1186/1471-2350-15-72. Review.

17.

Targeted next-generation sequencing of deafness genes in hearing-impaired individuals uncovers informative mutations.

Vona B, Müller T, Nanda I, Neuner C, Hofrichter MA, Schröder J, Bartsch O, Läßig A, Keilmann A, Schraven S, Kraus F, Shehata-Dieler W, Haaf T.

Genet Med. 2014 Dec;16(12):945-53. doi: 10.1038/gim.2014.65. Epub 2014 May 29.

18.

A RAD-tag genetic map for the platyfish (Xiphophorus maculatus) reveals mechanisms of karyotype evolution among teleost fish.

Amores A, Catchen J, Nanda I, Warren W, Walter R, Schartl M, Postlethwait JH.

Genetics. 2014 Jun;197(2):625-41. doi: 10.1534/genetics.114.164293. Epub 2014 Apr 2.

19.

Sex chromosome polymorphism in guppies.

Nanda I, Schories S, Tripathi N, Dreyer C, Haaf T, Schmid M, Schartl M.

Chromosoma. 2014 Aug;123(4):373-83. doi: 10.1007/s00412-014-0455-z. Epub 2014 Mar 28.

PMID:
24676866
20.

A Boy with an LCR3/4-Flanked 10q22.3q23.2 Microdeletion and Uncommon Phenotypic Features.

Petrova E, Neuner C, Haaf T, Schmid M, Wirbelauer J, Jurkutat A, Wermke K, Nanda I, Kunstmann E.

Mol Syndromol. 2014 Jan;5(1):19-24. doi: 10.1159/000355847. Epub 2013 Nov 2.

21.

Disruption of the ATE1 and SLC12A1 Genes by Balanced Translocation in a Boy with Non-Syndromic Hearing Loss.

Vona B, Neuner C, El Hajj N, Schneider E, Farcas R, Beyer V, Zechner U, Keilmann A, Poot M, Bartsch O, Nanda I, Haaf T.

Mol Syndromol. 2014 Jan;5(1):3-10. doi: 10.1159/000355443. Epub 2013 Oct 4.

22.

Widespread differences in cortex DNA methylation of the "language gene" CNTNAP2 between humans and chimpanzees.

Schneider E, El Hajj N, Richter S, Roche-Santiago J, Nanda I, Schempp W, Riederer P, Navarro B, Bontrop RE, Kondova I, Scholz CJ, Haaf T.

Epigenetics. 2014 Apr;9(4):533-45. doi: 10.4161/epi.27689. Epub 2014 Jan 16.

23.

Partial trisomy 1q41-qter and partial trisomy 9pter-9q21.32 in a newborn infant: an array CGH analysis and review.

Akalin I, Bozdag S, Spielmann M, Basaran SY, Nanda I, Klopocki E.

Am J Med Genet A. 2014 Feb;164A(2):490-4. doi: 10.1002/ajmg.a.36278. Epub 2013 Dec 5. Review.

PMID:
24311106
24.

Broad DNA methylation changes of spermatogenesis, inflammation and immune response-related genes in a subgroup of sperm samples for assisted reproduction.

Schütte B, El Hajj N, Kuhtz J, Nanda I, Gromoll J, Hahn T, Dittrich M, Schorsch M, Müller T, Haaf T.

Andrology. 2013 Nov;1(6):822-9. doi: 10.1111/j.2047-2927.2013.00122.x. Epub 2013 Aug 28.

25.

Confirmation of GRHL2 as the gene for the DFNA28 locus.

Vona B, Nanda I, Neuner C, Müller T, Haaf T.

Am J Med Genet A. 2013 Aug;161A(8):2060-5. doi: 10.1002/ajmg.a.36017. Epub 2013 Jun 27.

26.

Deep intronic 'mutations' cause hemophilia A: application of next generation sequencing in patients without detectable mutation in F8 cDNA.

Pezeshkpoor B, Zimmer N, Marquardt N, Nanda I, Haaf T, Budde U, Oldenburg J, El-Maarri O.

J Thromb Haemost. 2013 Sep;11(9):1679-87. doi: 10.1111/jth.12339.

27.

Novel form of X-linked nonsyndromic hearing loss with cochlear malformation caused by a mutation in the type IV collagen gene COL4A6.

Rost S, Bach E, Neuner C, Nanda I, Dysek S, Bittner RE, Keller A, Bartsch O, Mlynski R, Haaf T, Müller CR, Kunstmann E.

Eur J Hum Genet. 2014 Feb;22(2):208-15. doi: 10.1038/ejhg.2013.108. Epub 2013 May 29.

28.

Mild haemophilia A in a female patient with a large X-chromosomal deletion and a missense mutation in the F8 gene--a case report.

Rost S, Aumann V, Nanda I, Oldenburg J, Müller CR.

Haemophilia. 2013 Sep;19(5):e310-3. doi: 10.1111/hae.12190. Epub 2013 May 28. No abstract available.

PMID:
23710598
29.

ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticity.

Hirata H, Nanda I, van Riesen A, McMichael G, Hu H, Hambrock M, Papon MA, Fischer U, Marouillat S, Ding C, Alirol S, Bienek M, Preisler-Adams S, Grimme A, Seelow D, Webster R, Haan E, MacLennan A, Stenzel W, Yap TY, Gardner A, Nguyen LS, Shaw M, Lebrun N, Haas SA, Kress W, Haaf T, Schellenberger E, Chelly J, Viot G, Shaffer LG, Rosenfeld JA, Kramer N, Falk R, El-Khechen D, Escobar LF, Hennekam R, Wieacker P, Hübner C, Ropers HH, Gecz J, Schuelke M, Laumonnier F, Kalscheuer VM.

Am J Hum Genet. 2013 May 2;92(5):681-95. doi: 10.1016/j.ajhg.2013.03.021. Epub 2013 Apr 25.

30.

Live-born trisomy 22: patient report and review.

Heinrich T, Nanda I, Rehn M, Zollner U, Frieauff E, Wirbelauer J, Grimm T, Schmid M.

Mol Syndromol. 2013 Jan;3(6):262-9. doi: 10.1159/000346189. Epub 2013 Jan 11.

31.

The hemiphractid frogs. Phylogeny, embryology, life history, and cytogenetics.

Schmid M, Steinlein C, Bogart JP, Feichtinger W, Haaf T, Nanda I, del Pino EM, Duellman WE, Hedges SB.

Cytogenet Genome Res. 2012;138(2-4):69-384. doi: 10.1159/000343460. Epub 2013 Jan 23. No abstract available.

32.

FancJ/Brip1 helicase protects against genomic losses and gains in vertebrate cells.

Kitao H, Nanda I, Sugino RP, Kinomura A, Yamazoe M, Arakawa H, Schmid M, Innan H, Hiom K, Takata M.

Genes Cells. 2011 Jun;16(6):714-27. doi: 10.1111/j.1365-2443.2011.01523.x.

33.

Roles of brca2 (fancd1) in oocyte nuclear architecture, gametogenesis, gonad tumors, and genome stability in zebrafish.

Rodríguez-Marí A, Wilson C, Titus TA, Cañestro C, BreMiller RA, Yan YL, Nanda I, Johnston A, Kanki JP, Gray EM, He X, Spitsbergen J, Schindler D, Postlethwait JH.

PLoS Genet. 2011 Mar;7(3):e1001357. doi: 10.1371/journal.pgen.1001357. Epub 2011 Mar 31.

34.

Synteny conservation of chicken macrochromosomes 1-10 in different avian lineages revealed by cross-species chromosome painting.

Nanda I, Benisch P, Fetting D, Haaf T, Schmid M.

Cytogenet Genome Res. 2011;132(3):165-81. doi: 10.1159/000322358. Epub 2010 Nov 22.

PMID:
21099208
35.

Cross-species chromosome painting corroborates microchromosome fusion during karyotype evolution of birds.

Hansmann T, Nanda I, Volobouev V, Yang F, Schartl M, Haaf T, Schmid M.

Cytogenet Genome Res. 2009;126(3):281-304. doi: 10.1159/000251965. Epub 2010 Jan 6.

PMID:
20068299
36.

Sex determination and sex chromosome evolution: insights from medaka.

Kondo M, Nanda I, Schmid M, Schartl M.

Sex Dev. 2009;3(2-3):88-98. doi: 10.1159/000223074. Epub 2009 Aug 10. Review.

PMID:
19684454
37.

High tandem repeat content in the genome of the short-lived annual fish Nothobranchius furzeri: a new vertebrate model for aging research.

Reichwald K, Lauber C, Nanda I, Kirschner J, Hartmann N, Schories S, Gausmann U, Taudien S, Schilhabel MB, Szafranski K, Glöckner G, Schmid M, Cellerino A, Schartl M, Englert C, Platzer M.

Genome Biol. 2009 Feb 11;10(2):R16. doi: 10.1186/gb-2009-10-2-r16.

38.

Distribution of (TTAGGG)n telomeric sequences in karyotypes of the Xenopus species complex.

Nanda I, Fugate M, Steinlein C, Schmid M.

Cytogenet Genome Res. 2008;122(3-4):396-400. doi: 10.1159/000167828. Epub 2009 Jan 30.

PMID:
19188711
39.

Synteny conservation of the Z chromosome in 14 avian species (11 families) supports a role for Z dosage in avian sex determination.

Nanda I, Schlegelmilch K, Haaf T, Schartl M, Schmid M.

Cytogenet Genome Res. 2008;122(2):150-6. doi: 10.1159/000163092. Epub 2008 Dec 18.

PMID:
19096210
40.

Fanconi anemia: causes and consequences of genetic instability.

Kalb R, Neveling K, Nanda I, Schindler D, Hoehn H.

Genome Dyn. 2006;1:218-42. doi: 10.1159/000092510. Review.

PMID:
18724063
41.

Governing sex determination in fish: regulatory putsches and ephemeral dictators.

Volff JN, Nanda I, Schmid M, Schartl M.

Sex Dev. 2007;1(2):85-99. doi: 10.1159/000100030. Review.

42.

Molecular analysis of the sex-determining region of the platyfish Xiphophorus maculatus.

Schultheis C, Zhou Q, Froschauer A, Nanda I, Selz Y, Schmidt C, Matschl S, Wenning M, Veith AM, Naciri M, Hanel R, Braasch I, Dettai A, Böhne A, Ozouf-Costaz C, Chilmonczyk S, Ségurens B, Couloux A, Bernard-Samain S, Schmid M, Schartl M, Volff JN.

Zebrafish. 2006;3(3):299-309. doi: 10.1089/zeb.2006.3.299.

PMID:
18377211
43.

Disruption of the FA/BRCA pathway in bladder cancer.

Neveling K, Kalb R, Florl AR, Herterich S, Friedl R, Hoehn H, Hader C, Hartmann FH, Nanda I, Steinlein C, Schmid M, Tonnies H, Hurst CD, Knowles MA, Hanenberg H, Schulz WA, Schindler D.

Cytogenet Genome Res. 2007;118(2-4):166-76.

PMID:
18000367
44.

Automictic reproduction in interspecific hybrids of poeciliid fish.

Lampert KP, Lamatsch DK, Fischer P, Epplen JT, Nanda I, Schmid M, Schartl M.

Curr Biol. 2007 Nov 20;17(22):1948-53. Epub 2007 Nov 1.

45.

Stable inheritance of host species-derived microchromosomes in the gynogenetic fish Poecilia formosa.

Nanda I, Schlupp I, Lamatsch DK, Lampert KP, Schmid M, Schartl M.

Genetics. 2007 Oct;177(2):917-26. Epub 2007 Aug 24.

46.

Chromosome repatterning in three representative parrots (Psittaciformes) inferred from comparative chromosome painting.

Nanda I, Karl E, Griffin DK, Schartl M, Schmid M.

Cytogenet Genome Res. 2007;117(1-4):43-53.

PMID:
17675844
47.

The DNA sequence of medaka chromosome LG22.

Sasaki T, Shimizu A, Ishikawa SK, Imai S, Asakawa S, Murayama Y, Khorasani MZ, Mitani H, Furutani-Seiki M, Kondoh H, Nanda I, Schmid M, Schartl M, Nonaka M, Takeda H, Hori H, Himmelbauer H, Shima A, Shimizu N.

Genomics. 2007 Jan;89(1):124-33. Epub 2006 Oct 24.

48.

Genomic organization of the sex-determining and adjacent regions of the sex chromosomes of medaka.

Kondo M, Hornung U, Nanda I, Imai S, Sasaki T, Shimizu A, Asakawa S, Hori H, Schmid M, Shimizu N, Schartl M.

Genome Res. 2006 Jul;16(7):815-26. Epub 2006 Jun 2.

49.

Cytogenetics of the bleak (Alburnus alburnus), with special emphasis on the B chromosomes.

Schmid M, Ziegler CG, Steinlein C, Nanda I, Schartl M.

Chromosome Res. 2006;14(3):231-42. Epub 2006 Apr 20.

PMID:
16628494
50.

Extensive gross genomic rearrangements between chicken and Old World vultures (Falconiformes: Accipitridae).

Nanda I, Karl E, Volobouev V, Griffin DK, Schartl M, Schmid M.

Cytogenet Genome Res. 2006;112(3-4):286-95.

PMID:
16484785

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