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There are 22148 results for: content related to: Seeing the Wood for the Trees: A Minimal Reference Phylogeny for the Human Y Chromosome

  1. Simultaneous Analysis of Hundreds of Y-Chromosomal SNPs for High-Resolution Paternal Lineage Classification using Targeted Semiconductor Sequencing

    Human Mutation

    Volume 36, Issue 1, January 2015, Pages: 151–159, Arwin Ralf, Mannis van Oven, Kaiyin Zhong and Manfred Kayser

    Version of Record online : 27 NOV 2014, DOI: 10.1002/humu.22713

  2. You have full text access to this OnlineOpen article
    Gene Conversion Violates the Stepwise Mutation Model for Microsatellites in Y-Chromosomal Palindromic Repeats

    Human Mutation

    Volume 35, Issue 5, May 2014, Pages: 609–617, Patricia Balaresque, Turi E. King, Emma J. Parkin, Evelyne Heyer, Denise Carvalho-Silva, Thirsa Kraaijenbrink, Peter de Knijff, Chris Tyler-Smith and Mark A. Jobling

    Version of Record online : 22 APR 2014, DOI: 10.1002/humu.22542

  3. HAPLOFIND: A New Method for High-Throughput mtDNA Haplogroup Assignment

    Human Mutation

    Volume 34, Issue 9, September 2013, Pages: 1189–1194, Dario Vianello, Federica Sevini, Gastone Castellani, Laura Lomartire, Miriam Capri and Claudio Franceschi

    Version of Record online : 12 JUN 2013, DOI: 10.1002/humu.22356

  4. You have full text access to this OnlineOpen article
    Simultaneous Whole Mitochondrial Genome Sequencing with Short Overlapping Amplicons Suitable for Degraded DNA Using the Ion Torrent Personal Genome Machine

    Human Mutation

    Volume 36, Issue 12, December 2015, Pages: 1236–1247, Lakshmi Chaitanya, Arwin Ralf, Mannis van Oven, Tomasz Kupiec, Joseph Chang, Robert Lagacé and Manfred Kayser

    Version of Record online : 8 OCT 2015, DOI: 10.1002/humu.22905

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    Fine Time Scaling of Purifying Selection on Human Nonsynonymous mtDNA Mutations Based on the Worldwide Population Tree and Mother–Child Pairs

    Human Mutation

    Volume 36, Issue 11, November 2015, Pages: 1100–1111, Bruno Cavadas, Pedro Soares, Rui Camacho, Andreia Brandão, Marta D. Costa, Verónica Fernandes, Joana B. Pereira, Teresa Rito, David C. Samuels and Luisa Pereira

    Version of Record online : 25 AUG 2015, DOI: 10.1002/humu.22849

  6. mit-o-matic: A Comprehensive Computational Pipeline for Clinical Evaluation of Mitochondrial Variations from Next-Generation Sequencing Datasets

    Human Mutation

    Volume 36, Issue 4, April 2015, Pages: 419–424, Shamsudheen Karuthedath Vellarikkal, Heena Dhiman, Kandarp Joshi, Yasha Hasija, Sridhar Sivasubbu and Vinod Scaria

    Version of Record online : 31 MAR 2015, DOI: 10.1002/humu.22767

  7. Long-Standing Balancing Selection in the THBS4 Gene: Influence on Sex-Specific Brain Expression and Gray Matter Volumes in Alzheimer Disease

    Human Mutation

    Volume 34, Issue 5, May 2013, Pages: 743–753, Rachele Cagliani, Franca R. Guerini, Raquel Rubio-Acero, Francesca Baglio, Diego Forni, Cristina Agliardi, Ludovica Griffanti, Matteo Fumagalli, Uberto Pozzoli, Stefania Riva, Elena Calabrese, Martin Sikora, Ferran Casals, Giacomo P. Comi, Nereo Bresolin, Mario Cáceres, Mario Clerici and Manuela Sironi

    Version of Record online : 2 APR 2013, DOI: 10.1002/humu.22301

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    Y-chromosomal Binary Haplogroups in the Japanese Population and their Relationship to 16 Y-STR Polymorphisms

    Annals of Human Genetics

    Volume 71, Issue 4, July 2007, Pages: 480–495, I. Nonaka, K. Minaguchi and N. Takezaki

    Version of Record online : 2 FEB 2007, DOI: 10.1111/j.1469-1809.2006.00343.x

  9. Transition to Next Generation Analysis of the Whole Mitochondrial Genome: A Summary of Molecular Defects

    Human Mutation

    Volume 34, Issue 6, June 2013, Pages: 882–893, Sha Tang, Jing Wang, Victor Wei Zhang, Fang-Yuan Li, Megan Landsverk, Hong Cui, Cavatina K. Truong, Guoli Wang, Li Chieh Chen, Brett Graham, Fernando Scaglia, Eric S. Schmitt, William J. Craigen and Lee-Jun C. Wong

    Version of Record online : 2 APR 2013, DOI: 10.1002/humu.22307

  10. You have full text access to this OnlineOpen article
    Toward Male Individualization with Rapidly Mutating Y-Chromosomal Short Tandem Repeats

    Human Mutation

    Volume 35, Issue 8, August 2014, Pages: 1021–1032, Kaye N. Ballantyne, Arwin Ralf, Rachid Aboukhalid, Niaz M. Achakzai, Maria J. Anjos, Qasim Ayub, Jože Balažic, Jack Ballantyne, David J. Ballard, Burkhard Berger, Cecilia Bobillo, Mehdi Bouabdellah, Helen Burri, Tomas Capal, Stefano Caratti, Jorge Cárdenas, François Cartault, Elizeu F. Carvalho, Monica Carvalho, Baowen Cheng, Michael D. Coble, David Comas, Daniel Corach, Maria E. D'Amato, Sean Davison, Peter de Knijff, Maria Corazon A. De Ungria, Ronny Decorte, Tadeusz Dobosz, Berit M. Dupuy, Samir Elmrghni, Mateusz Gliwiński, Sara C. Gomes, Laurens Grol, Cordula Haas, Erin Hanson, Jürgen Henke, Lotte Henke, Fabiola Herrera-Rodríguez, Carolyn R. Hill, Gunilla Holmlund, Katsuya Honda, Uta-Dorothee Immel, Shota Inokuchi, Mark A. Jobling, Mahmoud Kaddura, Jong S. Kim, Soon H. Kim, Wook Kim, Turi E. King, Eva Klausriegler, Daniel Kling, Lejla Kovačević, Leda Kovatsi, Paweł Krajewski, Sergey Kravchenko, Maarten H. D. Larmuseau, Eun Young Lee, Ruediger Lessig, Ludmila A. Livshits, Damir Marjanović, Marek Minarik, Natsuko Mizuno, Helena Moreira, Niels Morling, Meeta Mukherjee, Patrick Munier, Javaregowda Nagaraju, Franz Neuhuber, Shengjie Nie, Premlaphat Nilasitsataporn, Takeki Nishi, Hye H. Oh, Jill Olofsson, Valerio Onofri, Jukka U. Palo, Horolma Pamjav, Walther Parson, Michal Petlach, Christopher Phillips, Rafal Ploski, Samayamantri P. R. Prasad, Dragan Primorac, Gludhug A. Purnomo, Josephine Purps, Hector Rangel-Villalobos, Krzysztof Rębała, Budsaba Rerkamnuaychoke, Danel Rey Gonzalez, Carlo Robino, Lutz Roewer, Alexandra Rosa, Antti Sajantila, Andrea Sala, Jazelyn M. Salvador, Paula Sanz, Cornelia Schmitt, Anil K. Sharma, Dayse A. Silva, Kyoung-Jin Shin, Titia Sijen, Miriam Sirker, Daniela Siváková, Vedrana Škaro, Carlos Solano-Matamoros, Luis Souto, Vlastimil Stenzl, Herawati Sudoyo, Denise Syndercombe-Court, Adriano Tagliabracci, Duncan Taylor, Andreas Tillmar, Iosif S. Tsybovsky, Chris Tyler-Smith, Kristiaan J. van der Gaag, Daniel Vanek, Antónia Völgyi, Denise Ward, Patricia Willemse, Eric P.H. Yap, Rita Y.Y. Yong, Irena Zupanič Pajnič and Manfred Kayser

    Version of Record online : 14 JUL 2014, DOI: 10.1002/humu.22599

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    Variation Interpretation Predictors: Principles, Types, Performance, and Choice

    Human Mutation

    Volume 37, Issue 6, June 2016, Pages: 579–597, Abhishek Niroula and Mauno Vihinen

    Version of Record online : 15 APR 2016, DOI: 10.1002/humu.22987

  12. Y chromosome haplogroups: A correlation with testicular dysgenesis syndrome?

    APMIS

    Volume 111, Issue 1, January 2003, Pages: 106–114, KEN McELREAVEY and LLUIS QUINTANA-MURCI

    Version of Record online : 6 MAY 2003, DOI: 10.1034/j.1600-0463.2003.11101151.x

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    Mutant TP53 Posttranslational Modifications: Challenges and Opportunities

    Human Mutation

    Volume 35, Issue 6, June 2014, Pages: 738–755, Thuy-Ai Nguyen, Daniel Menendez, Michael A. Resnick and Carl W. Anderson

    Version of Record online : 11 FEB 2014, DOI: 10.1002/humu.22506

  14. Lack of association between Y chromosome haplogroups and male infertility in Japanese men

    American Journal of Medical Genetics Part A

    Volume 116A, Issue 2, 15 January 2003, Pages: 152–158, Cláudia M.B. Carvalho, Masato Fujisawa, Toshiro Shirakawa, Akinobu Gotoh, Sadao Kamidono, Tatiana Freitas Paulo, Sidney E.B. Santos, Juliane Rocha, Sérgio D.J. Pena and Fabrício R. Santos

    Version of Record online : 5 SEP 2002, DOI: 10.1002/ajmg.a.10827

  15. TARDBP and FUS Mutations Associated with Amyotrophic Lateral Sclerosis: Summary and Update

    Human Mutation

    Volume 34, Issue 6, June 2013, Pages: 812–826, Serena Lattante, Guy A. Rouleau and Edor Kabashi

    Version of Record online : 29 APR 2013, DOI: 10.1002/humu.22319

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    MSeqDR: A Centralized Knowledge Repository and Bioinformatics Web Resource to Facilitate Genomic Investigations in Mitochondrial Disease

    Human Mutation

    Volume 37, Issue 6, June 2016, Pages: 540–548, Lishuang Shen, Maria Angela Diroma, Michael Gonzalez, Daniel Navarro-Gomez, Jeremy Leipzig, Marie T. Lott, Mannis van Oven, Douglas C. Wallace, Colleen Clarke Muraresku, Zarazuela Zolkipli-Cunningham, Patrick F. Chinnery, Marcella Attimonelli, Stephan Zuchner, Marni J. Falk and Xiaowu Gai

    Version of Record online : 21 MAR 2016, DOI: 10.1002/humu.22974

  17. You have full text access to this OnlineOpen article
    Pathogenic Mitochondrial tRNA Point Mutations: Nine Novel Mutations Affirm Their Importance as a Cause of Mitochondrial Disease

    Human Mutation

    Volume 34, Issue 9, September 2013, Pages: 1260–1268, Emma L. Blakely, John W. Yarham, Charlotte L. Alston, Kate Craig, Joanna Poulton, Charlotte Brierley, Soo-Mi Park, Andrew Dean, John H. Xuereb, Kirstie N. Anderson, Alistair Compston, Chris Allen, Saba Sharif, Peter Enevoldson, Martin Wilson, Simon R. Hammans, Douglass M. Turnbull, Robert McFarland and Robert W. Taylor

    Version of Record online : 14 AUG 2013, DOI: 10.1002/humu.22358

  18. Mitochondrial DNA Rearrangements in Health and Disease—A Comprehensive Study

    Human Mutation

    Volume 35, Issue 1, January 2014, Pages: 1–14, Joana Damas, David C. Samuels, João Carneiro, António Amorim and Filipe Pereira

    Version of Record online : 18 OCT 2013, DOI: 10.1002/humu.22452

  19. Functional Assays for Analysis of Variants of Uncertain Significance in BRCA2

    Human Mutation

    Volume 35, Issue 2, February 2014, Pages: 151–164, Lucia Guidugli, Aura Carreira, Sandrine M. Caputo, Asa Ehlen, Alvaro Galli, Alvaro N.A. Monteiro, Susan L. Neuhausen, Thomas V.O. Hansen, Fergus J. Couch, Maaike P.G. Vreeswijk and ; on behalf of the ENIGMA consortium

    Version of Record online : 3 DEC 2013, DOI: 10.1002/humu.22478

  20. On Human Disease-Causing Amino Acid Variants: Statistical Study of Sequence and Structural Patterns

    Human Mutation

    Volume 36, Issue 5, May 2015, Pages: 524–534, Marharyta Petukh, Tugba G. Kucukkal and Emil Alexov

    Version of Record online : 6 APR 2015, DOI: 10.1002/humu.22770