Хайлтын үр дүнгүүд - Katayoon Darvishi
- 6-н 1 - 6 үр дүнгүүдийг харуулж байна
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1
The Indian origin of paternal haplogroup R1a1* substantiates the autochthonous origin of Brahmins and the caste system -н Swarkar Sharma, Ekta Rai, Prithviraj Sharma, Mamata Jena, Shweta Singh, Katayoon Darvishi, Audesh Bhat, A.J.S. Bhanwer, Pramod Kumar Tiwari, R. Bamezai
Хэвлэсэн 2009Artigo -
2
Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs -н Joshua M. Korn, Finny G. Kuruvilla, Steven A. McCarroll, Alec Wysoker, James Nemesh, Simon Cawley, Earl Hubbell, Jim Veitch, Patrick Collins, Katayoon Darvishi, Charles Lee, Marcia M. Nizzari, Stacey B. Gabriel, Shaun Purcell, Mark J. Daly, David Altshuler
Хэвлэсэн 2008Artigo -
3
Prevalence and penetrance of <i><scp>ZFPM2</scp></i> mutations and deletions causing congenital diaphragmatic hernia -н Mauro Longoni, Meaghan Russell, Frances A. High, Katayoon Darvishi, Faouzi I. Maalouf, Alireza Kashani, Adam Tracy, Caroline Coletti, Marı́a Loscertales, Kasper Lage, Kate G. Ackerman, Susan A. Woods, Catherine Ward‐Melver, Dan Andrews, C. Lee, Barbara R. Pober, Patricia K. Donahoe
Хэвлэсэн 2014Artigo -
4
Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants -н Dalila Pinto, Katayoon Darvishi, Xinghua Shi, Diana Rajan, Diane Rigler, Tomas Fitzgerald, Anath C. Lionel, Bhooma Thiruvahindrapuram, Jeffrey R. MacDonald, Ryan E. Mills, Aparna Prasad, Kristin Noonan, Susan Gribble, Elena Prigmore, Patricia K. Donahoe, Richard S. Smith, Ji Hyeon Park, Matthew E. Hurles, Nigel P. Carter, Charles Lee, Stephen W. Scherer, Lars Feuk
Хэвлэсэн 2011Artigo -
5
Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing -н Hansoo Park, Jong‐Il Kim, Young Seok Ju, Ömer Gökçümen, Ryan E. Mills, Sheehyun Kim, Seungbok Lee, Dongwhan Suh, Dongwan Hong, Hyunseok P. Kang, Yun Joo Yoo, Jong-Yeon Shin, Hyun‐Jin Kim, Maryam Yavartanoo, Young Wha Chang, Jung‐Sook Ha, Wilson Chong, Ga‐Ram Hwang, Katayoon Darvishi, Hye‐Ran Kim, Song Ju Yang, Kap-Seok Yang, Hyungtae Kim, Matthew E. Hurles, Stephen W. Scherer, Nigel P. Carter, Chris Tyler‐Smith, Charles Lee, Jeong‐Sun Seo
Хэвлэсэн 2010Artigo -
6
Integrating common and rare genetic variation in diverse human populations -н David Altshuler, Richard A Gibbs, Leena Peltonen, David Altshuler, Richard A Gibbs, Leena Peltonen, Emmanouil T. Dermitzakis, S. F. Schaffner, Fuli Yu, Leena Peltonen, Emmanouil T. Dermitzakis, Penelope E. Bonnen, David Altshuler, Richard A Gibbs, Paul I. W. de Bakker, Panos Deloukas, Stacey B. Gabriel, Rhian Gwilliam, Sarah Hunt, Michael Inouye, Xiaoming Jia, Aarno Palotie, Melissa Parkin, Pamela Whittaker, Fuli Yu, Kyle Chang, Alicia Hawes, Lora Lewis, Yanru Ren, David A. Wheeler, Richard A. Gibbs, Donna M. Muzny, C. Barnes, Katayoon Darvishi, Matthew E. Hurles, Joshua M. Korn, Kati Kristiansson, Charles Lee, Steven A. McCarrol, James Nemesh, Emmanouil T. Dermitzakis, Alon Keinan, Stephen B. Montgomery, Samuela Pollack, Alkes L. Price, Nicole Soranzo, Penelope E. Bonnen, Richard A Gibbs, Claudia Gonzaga‐Jauregui, Alon Keinan, Alkes L. Price, Fuli Yu, Verneri Anttila, Wendy Brodeur, Mark J. Daly, Stephen Leslie, Gil McVean, Loukas Moutsianas, Huy Nguyen, S. F. Schaffner, Qingrun Zhang, Mohammed J. R. Ghori, Ralph McGinnis, William McLaren, Samuela Pollack, Alkes L. Price, S. F. Schaffner, Fumihiko Takeuchi, Sharon R. Grossman, Ilya Shlyakhter, Elizabeth Hostetter, Pardis C. Sabeti, Clement Adebamowo, Morris W. Foster, Deborah R Gordon, Júlio Licinio, María Cristina Manca, Patricia A. Marshall, Ichiro Matsuda, Duncan Ngare, Vivian Ota Wang, Deepa Reddy, Charles N. Rotimi, Charmaine Royal, Richard R. Sharp, Changqing Zeng, Lisa Brooks, Jean E. McEwen
Хэвлэсэн 2010Artigo
Хайх хэрэгслүүд:
Холбогдох сэдвүүд
Biology
Gene
Genetics
Genome
Computational biology
Copy-number variation
Allele
Computer science
Genetic association
Genomics
Genotype
Geography
Haplotype
Human genome
Medicine
Population
SNP genotyping
Single-nucleotide polymorphism
1000 Genomes Project
Allele frequency
Ancient history
Benchmark (surveying)
Bioinformatics
Cartography
Caste
Comparative genomic hybridization
Concordance
Copy number analysis
DNA sequencing
Data mining