Estimating time to the most recent common ancestor (TMRCA): comparison and application of eight methods (English)
- New search for: Zhou, J.
- New search for: Teo, Y. Y.
- New search for: Zhou, J.
- New search for: Teo, Y. Y.
In:
EUROPEAN JOURNAL OF HUMAN GENETICS
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24
, 8
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1195-1201
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2016
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ISSN:
- Article (Journal) / Print
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Title:Estimating time to the most recent common ancestor (TMRCA): comparison and application of eight methods
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Contributors:Zhou, J. ( author ) / Teo, Y. Y. ( author )
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Published in:EUROPEAN JOURNAL OF HUMAN GENETICS ; 24, 8 ; 1195-1201
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Publisher:
- New search for: Nature Publishing Group
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Publication date:2016-01-01
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Size:7 pages
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ISSN:
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Type of media:Article (Journal)
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Type of material:Print
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Language:English
- New search for: 599.435
- Further information on Dewey Decimal Classification
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Classification:
DDC: 599.435 -
Source:
© Metadata Copyright the British Library Board and other contributors. All rights reserved.
Table of contents – Volume 24, Issue 8
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 1097
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Genetic discovery in multi-ethnic populationsTraylor, M. / Lewis, C. M. et al. | 2016
- 1099
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A decision tool to guide the ethics review of a challenging breed of emerging genomic projectsJoly, Y. / So, D. / Osien, G. / Crimi, L. / Bobrow, M. / Chalmers, D. / Wallace, S. E. / Zeps, N. / Knoppers, B. et al. | 2016
- 1104
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Post-mortem testing; germline BRCA1/2 variant detection using archival FFPE non-tumor tissue. A new paradigm in genetic counselingPetersen, A. H. / Aagaard, M. M. / Nielsen, H. R. / Steffensen, K. D. / Waldstrom, M. / Bojesen, A. et al. | 2016
- 1112
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High incidence and variable clinical outcome of cardiac hypertrophy due to ACAD9 mutations in childhoodCollet, M. / Assouline, Z. / Bonnet, D. / Rio, M. e. / Iserin, F. / Sidi, D. / Goldenberg, A. / Lardennois, C. / Metodiev, M. D. / Haberberger, B. et al. | 2016
- 1117
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A novel splicing mutation in the IQSEC2 gene that modulates the phenotype severity in a family with intellectual disabilityMadrigal, I. / Alvarez-Mora, M. I. / Rosell, J. / Rodriguez-Revenga, L. / Karlberg, O. / Sauer, S. / Syvanen, A. C. / Mila, M. et al. | 2016
- 1124
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Mutations in RIT1 cause Noonan syndrome with possible juvenile myelomonocytic leukemia but are not involved in acute lymphoblastic leukemiaCave, H. e. / Caye, A. / Ghedira, N. / Capri, Y. / Pouvreau, N. / Fillot, N. / Trimouille, A. / Vignal, C. / Fenneteau, O. / Alembik, Y. et al. | 2016
- 1132
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Duplication of PTHLH causes osteochondroplasia with a combined brachydactyly type E/A1 phenotype with disturbed bone maturation and rhizomeliaFlottmann, R. / Sowinska-Seidler, A. / Lavie, J. / Chateil, J. F. / Lacombe, D. / Mundlos, S. / Horn, D. / Spielmann, M. et al. | 2016
- 1137
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Heritability of non-speech auditory processing skillsBrewer, C. C. / Zalewski, C. K. / King, K. A. / Zobay, O. / Riley, A. / Ferguson, M. A. / Bird, J. E. / McCabe, M. M. / Hood, L. J. / Drayna, D. et al. | 2016
- 1145
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De novo loss-of-function mutations in WAC cause a recognizable intellectual disability syndrome and learning deficits in DrosophilaLugtenberg, D. / Reijnders, M. R. / Fenckova, M. / Bijlsma, E. K. / Bernier, R. / van Bon, B. W. / Smeets, E. / Vulto-van Silfhout, A. T. / Bosch, D. / Eichler, E. E. et al. | 2016
- 1154
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Genes for spinocerebellar ataxia with blindness and deafness (SCABD/SCAR3, MIM# 271250 and SCABD2)Guissart, C. / Drouot, N. / Oncel, I. / Leheup, B. / Gershoni-Barush, R. / Muller, J. / Ferdinandusse, S. / Larrieu, L. / Anheim, M. / Arslan, E. A. et al. | 2016
- 1160
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Asymmetry of parental origin in long QT syndrome: preferential maternal transmission of KCNQ1 variants linked to channel dysfunctionItoh, H. / Berthet, M. / Fressart, V. / Denjoy, I. / Maugenre, S. / Klug, D. / Mizusawa, Y. / Makiyama, T. / Hofman, N. / Stallmeyer, B. et al. | 2016
- 1167
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Genomic complexity of urothelial bladder cancer revealed in urinary cfDNATogneri, F. S. / Ward, D. G. / Foster, J. M. / Devall, A. J. / Wojtowicz, P. / Alyas, S. / Vasques, F. R. / Oumie, A. / James, N. D. / Cheng, K. K. et al. | 2016
- 1175
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Multi-ethnic genome-wide association study identifies novel locus for type 2 diabetes susceptibilityCook, J. P. / Morris, A. P. et al. | 2016
- 1181
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Rare variant associations with waist-to-hip ratio in European-American and African-American women from the NHLBI-Exome Sequencing ProjectKan, M. / Auer, P. L. / Wang, G. T. / Bucasas, K. L. / Hooker, S. / Rodriguez, A. / Li, B. / Ellis, J. / Adrienne Cupples, L. / Ida Chen, Y. D. et al. | 2016
- 1188
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The effect of phenotypic outliers and non-normality on rare-variant association testingAuer, P. L. / Reiner, A. P. / Leal, S. M. et al. | 2016
- 1195
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Estimating time to the most recent common ancestor (TMRCA): comparison and application of eight methodsZhou, J. / Teo, Y. Y. et al. | 2016
- 1202
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The (in)famous GWAS P-value threshold revisited and updated for low-frequency variantsFadista, J. / Manning, A. K. / Florez, J. C. / Groop, L. et al. | 2016
- 1206
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A novel multiple joint dislocation syndrome associated with a homozygous nonsense variant in the EXOC6B geneGirisha, K. M. / Kortum, F. / Shah, H. / Alawi, M. / Dalal, A. / Bhavani, G. S. / Kutsche, K. et al. | 2016
- 1211
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Variants of the ACTG2 gene correlate with degree of severity and presence of megacystis in chronic intestinal pseudo-obstructionMatera, I. / Rusmini, M. / Guo, Y. / Lerone, M. / Li, J. / Zhang, J. / Di Duca, M. / Nozza, P. / Mosconi, M. / Prato, A. P. et al. | 2016
- 1216
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Prominent scapulae mimicking an inherited myopathy expands the phenotype of CHD7-related diseaseO'Grady, G. L. / Ma, A. / Sival, D. / Wong, M. T. / Peduto, T. / Menezes, M. P. / Young, H. / Waddell, L. / Ghaoui, R. / Needham, M. et al. | 2016
- 1220
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Distal acroosteolysis, poikiloderma and joint stiffness: a novel laminopathy?Sewairi, W. / Assiri, A. / Patel, N. / Alhashem, A. / Alkuraya, F. S. et al. | 2016
- 1223
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Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disabilityAnsar, M. / Jan, A. / Santos-Cortez, R. L. / Wang, X. / Suliman, M. / Acharya, A. / Habib, R. / Abbe, I. / Ali, G. / Lee, K. et al. | 2016
- 1228
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The HLA-DQβ1 insertion is a strong achalasia risk factor and displays a geospatial north–south gradient among EuropeansBecker, J. / Haas, S. L. / Mokrowiecka, A. / Wasielica-Berger, J. / Ateeb, Z. / Bister, J. / Elbe, P. / Kowalski, M. / Gawron-Kiszka, M. / Majewski, M. et al. | 2016
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Clinical utility gene card for: Meckel syndrome – update 2016Bergmann, C. / Frank, V. / Salonen, R. et al. | 2016
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Clinical utility gene card for: Familial platelet disorder with associated myeloid malignanciesRipperger, T. / Tawana, K. / Kratz, C. / Schlegelberger, B. / Fitzgibbon, J. / Steinemann, D. et al. | 2016
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Clinical utility gene card for: Peters plus syndromeJaeken, J. / Lefeber, D. J. / Matthijs, G. et al. | 2016