Rare and common variants: twenty arguments

Cited by (998)

Items 301–400 of 998

1. Functional classification of 15 million SNPs detected from diverse chicken populations
   Almas Gheyas, Clarissa Boschiero, Lél Eöry, H. Ralph, Richard I Kuo, J.A. Woolliams, David W. Burt · 2015 · DNA Research
2. Aetiological coding sequence variants in non-syndromic premature ovarian failure: From genetic linkage analysis to next generation sequencing
   Paul Laissue · 2015 · Molecular and Cellular Endocrinology
3. Alleles versus mutations: Understanding the evolution of genetic architecture requires a molecular perspective on allelic origins
   David L. Remington · 2015 · Evolution
4. Importance of Genetic Studies in Consanguineous Populations for the Characterization of Novel Human Gene Functions
   Abdullah Mesut Erzurumluoglu, Hashem A. Shihab, Santiago Rodrı́guez, Tom R. Gaunt, Ian N.M. Day · 2016 · Annals of Human Genetics
5. Power and sample size calculations for high-throughput sequencing-based experiments
   Chung-I Li, David C. Samuels, Ying‐Yong Zhao, Yu Shyr, Yan Ping Guo · 2017 · Briefings in Bioinformatics
6. Association of Posttraumatic Stress Disorder With rs2267735 in the ADCYAP1R1 Gene: A Meta‐Analysis
   Mackenzie J. Lind, Marisa E. Marraccini, Christina M. Sheerin, Kaitlin E. Bountress, Silviu‐Alin Bacanu, Ananda B. Amstadter, Nicole R. Nugent · 2017 · Journal of Traumatic Stress
7. Inferring the Nature of Missing Heritability in Human Traits Using Data from the GWAS Catalog
   Eugenio López‐Cortegano, Armando Caballero · 2019 · Genetics
8. Electrophysiological Endophenotypes for Schizophrenia
   Emily M. Owens, Peter Bachman, David C. Glahn, Carrie E. Bearden · 2016 · Harvard Review of Psychiatry
9. Towards an integrated psycholinguistic, neurolinguistic, sensorimotor framework for speech production
   Gregory S. Hickok · 2013 · Language Cognition and Neuroscience
10. Next-Generation Statistical Genetics: Modeling, Penalization, and Optimization in High-Dimensional Data
    Kenneth L. Lange, Jeanette C. Papp, Janet S. Sinsheimer, Eric M. Sobel · 2013 · Annual Review of Statistics and Its Application
11. Genetic background affects epistatic interactions between two beneficial mutations
    Yinhua Wang, Carolina Díaz Arenas, Daniel M. Stoebel, Tim F. Cooper · 2012 · Biology Letters
12. Using information of relatives in genomic prediction to apply effective stratified medicine
    Sang Lee, Shalanee Weerasinghe, Naomi R. Wray, Michael Edward Goddard, Julius H. J. van der Werf · 2017 · Scientific Reports
13. A novel linkage-disequilibrium corrected genomic relationship matrix for SNP-heritability estimation and genomic prediction
    Boby Mathew, Jens Léon, Mikko J. Sillanpää · 2017 · Heredity
14. Genetic alterations in necrotizing enterocolitis
    Alain C. Cuna, Venkatesh Sampath · 2016 · Seminars in Perinatology
15. A Single Nucleotide Polymorphism in Osteonectin 3′ Untranslated Region Regulates Bone Volume and Is Targeted by miR-433
    Neha S. Dole, Kristina Kapinas, Catherine B. Kessler, Siu‐Pok Yee, Douglas J. Adams, Renata C. Pereira, Anne M. Delany · 2014 · Journal of Bone and Mineral Research
16. A Genome-Wide Association Analysis Reveals Epistatic Cancellation of Additive Genetic Variance for Root Length in Arabidopsis thaliana
    Jennifer Lachowiec, Xia Shen, Christine Queitsch, Örjan Carlborg · 2015 · PLoS Genetics
17. Comprehensive Functional Annotation of Seventy-One Breast Cancer Risk Loci
    Suhn K. Rhie, Simon G. Coetzee, Houtan Noushmehr, Chunli Yan, Jae Mun Kim, Christopher A. Haiman, Gerhard A. Coetzee · 2013 · PLoS ONE
18. Copy Number Variants in Obesity-Related Syndromes: Review and Perspectives on Novel Molecular Approaches
    Carla Sustek D’Angelo, Célia Priszkulnik Koiffmann · 2012 · Journal of Obesity
19. Cohesion and Joint Speech: Right Hemisphere Contributions to Synchronized Vocal Production
    Kyle M. Jasmin, Carolyn McGettigan, Zarinah Karim Agnew, Nadine Lavan, Oliver Josephs, Fred Cummins, Sophie Kerttu Scott · 2016 · Journal of Neuroscience
20. Genome-Wide Analysis of Protein-Coding Variants in Leprosy
    Hong Liu, Zhenzhen Wang, Yi Li, Gongqi Yu, Xi’an Fu, Chuan Wang, Wenting Liu, Yongxiang Yu, Fangfang Bao, Astrid K Irwanto et al. · 2017 · Journal of Investigative Dermatology
21. Endocrinology Meets Metabolomics: Achievements, Pitfalls, and Challenges
    Janina Tokarz, Mark Haid, Alexander Cecil, Cornelia P. Prehn, Anna Artati, Gabriele Möller, Jerzy Adamski · 2017 · Trends in Endocrinology and Metabolism
22. Exploring public genomics data for population pharmacogenomics
    Kleanthi Lakiotaki, Alexandros Kanterakis, Evgenia Kartsaki, Θεοδώρα Κάτσιλα, George P. Patrinos, George Potamias · 2017 · PLoS ONE
23. APOL1 Nephropathy: A Population Genetics and Evolutionary Medicine Detective Story
    Etty Kruzel-Davila, Walter G. Wasser, Karl L. Skorecki · 2017 · Seminars in Nephrology
24. Subthalamic Nucleus Neurons Differentially Encode Early and Late Aspects of Speech Production
    Witold J. Lipski, Ahmad Alhourani, Tara Pirnia, PW Jones, Christina Dastolfo‐Hromack, Leah Bernadette Helou, Donald J. Crammond, Susan Shaiman, Michael Walsh Dickey, Lori L. Holt et al. · 2018 · Journal of Neuroscience
25. A biological network-based regularized artificial neural network model for robust phenotype prediction from gene expression data
    Tianyu Kang, Wei Ding, Luoyan Zhang, Daniel Ziemek, Kourosh Zarringhalam · 2017 · BMC Bioinformatics
26. Recent Advances in the Genetics of Fractures in Osteoporosis
    Fjorda Koromani, Katerina Trajanoska, Fernando Rivadeneira, Ling Oei · 2019 · Frontiers in Endocrinology
27. Network dynamics of Broca’s area during word selection
    Christopher Richard Conner, Cihan Mehmet Kadipasaoglu, Harel Z. Shouval, Gregory S. Hickok, Nitin Tandon · 2019 · PLoS ONE
28. Evidence of gene–gene interaction in hidradenitis suppurativa: a nationwide registry study of Danish twins
    Rune Kjærsgaard Andersen, Signe Bedsted Clemmensen, Lisbeth Aagaard Larsen, Jacob Hjelmborg, Niels Ødum, Gregor B. E. Jemec, Kaare Christensen · 2021 · British Journal of Dermatology
29. Developments in our understanding of the genetic basis of birth defects
    Daniel M. Webber, Stewart L. MacLeod, Michael J. Bamshad, Gary M. Shaw, Richard H. Finnell, Sanjay S. Shete, John S. Witte, Stephen W. Erickson, Linda D. Murphy, Charlotte A. Hobbs · 2015 · Birth Defects Research Part A Clinical and Molecular Teratology
30. Rat Ultrasonic Vocalization Shows Features of a Modular Behavior
    Tobias Riede · 2014 · Journal of Neuroscience
31. Transcriptomics in type 2 diabetes: Bridging the gap between genotype and phenotype
    Christopher P. Jenkinson, Harald H.H. Göring, Rector Arya, John Blangero, Ravindranath Duggirala, Ralph A. DeFronzo · 2015 · Genomics Data
32. A cortical circuit for voluntary laryngeal control: Implications for the evolution language
    Gregory S. Hickok · 2016 · Psychonomic Bulletin & Review
33. Childhood risk factors for adulthood chronic kidney disease
    Michal Stern-Zimmer, Ronit Calderon‐Margalit, Karl L. Skorecki, Asaf Vivante · 2020 · Pediatric Nephrology
34. Environmentally induced ribosomal DNA (rDNA) instability in human cells and populations exposed to hexavalent chromium [Cr (VI)]
    Jianlin Lou, Shoukai Yu, Lingfang Feng, Xinnian Guo, Meng Wang, Alan Trindade Branco, Tao Li, Bernardo Lemos · 2021 · Environment International
35. Modeling Gene‐Environment Interactions With Quasi‐Natural Experiments
    Lauren Schmitz, Dalton Conley · 2015 · Journal of Personality
36. Kinetics genetics: Incorporating the concept of genomic balance into an understanding of quantitative traits
    James A. Birchler, Adam F. Johnson, Reiner A. Veitia · 2016 · Plant Science
37. A genome‐wide association study of copy number variations with umbilical hernia in swine
    Yi Long, Ying Su, Huashui Ai, Zhiyan Zhang, Bin Juan Yang, Guorong Ruan, Shijun Xiao, Xinjun Liao, Jun Ren, Lusheng Huang et al. · 2016 · Animal Genetics
38. Sensorimotor integration on a rapid time scale
    Jinhong Luo, Ninad B. Kothari, Cynthia F. Moss · 2017 · Proceedings of the National Academy of Sciences
39. Definitive roles of TOMM40-APOE-APOC1 variants in the Alzheimer's risk
    Alexander M. Kulminski, Ian Philipp, Leonardo Shu, Irina V. Culminskaya · 2021 · Neurobiology of Aging
40. Category Specific Spatial Dissociations of Parallel Processes Underlying Visual Naming
    Christopher Richard Conner, Guibin Chen, Thomas Allyn Pieters, Nitin Tandon · 2013 · Cerebral Cortex
41. Non-fluent speech following stroke is caused by impaired efference copy
    Lynda Feenaughty, Alexandra Basilakos, Leonardo Bonilha, Dirk‐Bart den Ouden, Chris Rorden, Brielle Caserta Stark, Julius Fridriksson · 2017 · Cognitive Neuropsychology
42. Formant compensation for auditory feedback with English vowels
    Takashi Mitsuya, Ewen MacDonald, Kevin G. Munhall, David W. Purcell · 2015 · The Journal of the Acoustical Society of America
43. Genome‐wide patterns of differentiation and spatially varying selection between postglacial recolonization lineages ofPopulus alba(Salicaceae), a widespread forest tree
    Kai N. Stölting, Margot Paris, Cécile Meier, Berthold Heinze, Stefano Castiglione, Dénes Bartha, Christian Lexer · 2015 · New Phytologist
44. The genetic heterogeneity of colorectal cancer predisposition - guidelines for gene discovery
    Marc‐Manuel Hahn, Richarda M. de Voer, Nicoline Hoogerbrugge, Marjolijn J. L. Ligtenberg, Roland P. Kuiper, Ad Geurts van Kessel · 2016 · Cellular Oncology
45. Association Analysis in Rice: From Application to Utilization
    Peng Zhang, Kaizhen Zhong, Muhammad Qasim Shahid, Hanhua Tong · 2016 · Frontiers in Plant Science
46. Impact of range expansions on current human genomic diversity
    Vítor C. Sousa, Stephan Peischl, Laurent Excoffier · 2014 · Current Opinion in Genetics & Development
47. Genetic architecture of quantitative traits and complex diseases
    Wenqing Fu, Timothy D. O’Connor, Joshua M. Akey · 2013 · Current Opinion in Genetics & Development
48. Genomic medicine and risk prediction across the disease spectrum
    Maritha J. Kotze, Hilmar Klaus Luckhoff, Armand V. Peeters, Karin Baatjes, Mardelle Schoeman, Lize van der Merwe, Kathleen A. Grant, Leslie R. Fisher, Nicole van der Merwe, Jacobus Pretorius et al. · 2015 · Critical Reviews in Clinical Laboratory Sciences
49. Genetic architecture of retinal and macular degenerative diseases: the promise and challenges of next-generation sequencing
    Rinki Ratnapriya, Anand Swaroop · 2013 · Genome Medicine
50. Sensitivity Analysis and Power for Instrumental Variable Studies
    Xuran Wang, Yang Jiang, Nancy Ruonan Zhang, Dylan S. Small · 2018 · Biometrics
51. Genotype imputation and reference panel: a systematic evaluation on haplotype size and diversity
    Wei-Yang Bai, Xiao-Wei Zhu, Peikuan Cong, Xue-Jun Zhang, John Brent Richards, Hou‐Feng Zheng · 2019 · Briefings in Bioinformatics
52. Inherited Rare, Deleterious Variants in ATM Increase Lung Adenocarcinoma Risk
    Myvizhi Esai Selvan, Marjorie Glass Zauderer, Charles M. Rudin, Siân Jones, Semanti Mukherjee, Kenneth Offit, Kenan Onel, Gad Rennert, Victor E. Velculescu, Steven M. Lipkin et al. · 2020 · Journal of Thoracic Oncology
53. The Same Ultra-Rapid Parallel Brain Dynamics Underpin the Production and Perception of Speech
    Amie Fairs, Amandine Michelas, Sophie Dufour, Kristof Strijkers · 2021 · Cerebral Cortex Communications
54. Variations with modest effects have an important role in the genetic background of type 2 diabetes and diabetes-related traits
    Hayato Fujita, Kazuo Hara, Nobuhiro Shojima, Momoko Horikoshi, Minoru Iwata, Yushi Hirota, Kazuyuki Tobe, Susumu Seino, Takashi Kadowaki · 2012 · Journal of Human Genetics
55. A Developmental Perspective on Attention-Deficit/Hyperactivity Disorder (ADHD)
    Susan B. Goodman Campbell, Jeffrey M. Halperin, Edmund J. S. Sonuga-Barke · 2014 · Springer eBooks
56. Advances in the genetic dissection of plant cell walls: tools and resources available in Miscanthus
    Gancho Slavov, Gordon G Allison, Maurice Bosch · 2013 · Frontiers in Plant Science
57. Accurate liability estimation improves power in ascertained case-control studies
    Omer Weissbrod, Christoph Lippert, Dan Geiger, David E. Heckerman · 2015 · Nature Methods
58. Mapping asthma-associated variants in admixed populations
    Tesfaye Mersha Baye · 2015 · Frontiers in Genetics
59. A rare missense variant in RCL1 segregates with depression in extended families.
    Amin, N, de Vrij, F M S, Baghdadi, M, Brouwer, R W W, van Rooij, J G J, Jovanova, O, Uitterlinden, A G, Hofman, A, Janssen, H L A, Darwish Murad, S et al. · 2018 · Molecular Psychiatry
60. Genome-Wide Association Analyses in the Model Rhizobium Ensifer meliloti
    Brendan Epstein, Reda A.I. Abou-Shanab, Abdelaal Shamseldin, Margaret R. Taylor, Joseph G. Guhlin, Liana T. Burghardt, Matthew S. Nelson, Michael Jay Sadowsky, Peter Tiffin · 2018 · mSphere
61. STAT5B mutations in heterozygous state have negative impact on height: another clue in human stature heritability
    Renata C. Scalco, Vivian Hwa, Horacio M. Domené, Héctor Jasper, Alicia Belgorosky, Roxana Marcela Marino, Alberto M. Pereira, Carlos André Tonelli, Jan Maarten Wit, Ron G. Rosenfeld et al. · 2015 · European Journal of Endocrinology
62. Neurolinguistic and machine-learning perspectives on direct speech BCIs for restoration of naturalistic communication
    Olga Iljina, Johanna Derix, Robin Tibor Schirrmeister, Andreas Schulze‐Bonhage, Peter L. Auer, Ad Aertsen, Tonio Ball · 2017 · Brain-Computer Interfaces
63. Uncovering the extensive trade-off between adaptive evolution and disease susceptibility
    Ji Tang, Maosheng Huang, Sha He, Junxiang Zeng, Hao Zhu · 2022 · Cell Reports
64. Integration of risk factor polygenic risk score with disease polygenic risk score for disease prediction
    Hyein Jung, Hae‐Un Jung, Eun Ju Baek, Shin Young Kwon, Ji‐One Kang, Ji Eun Lim, Bermseok Oh · 2024 · Communications Biology
65. Combining Family‐ and Population‐Based Imputation Data for Association Analysis of Rare and Common Variants in Large Pedigrees
    Mohamad Saad, Ellen M. Wijsman · 2014 · Genetic Epidemiology
66. Conditions for the validity of SNP-based heritability estimation
    James J. Lee, Carson C. Chow · 2014 · Human Genetics
67. Auditory Predictions and Prediction Errors in Response to Self-Initiated Vowels
    Franziska Knolle, Michael Schwartze, Erich Schröger, Sonja A. Kotz · 2019 · Frontiers in Neuroscience
68. The Neuroanatomy of Speech Processing: A Large-scale Lesion Study
    Corianne Rogalsky, Alexandra Basilakos, Chris Rorden, Sara B. Pillay, Arianna N. LaCroix, Lynsey M. Keator, Soren Mickelsen, Steven W. Anderson, Tracy E. Love, Julius Fridriksson et al. · 2022 · Journal of Cognitive Neuroscience
69. Uncovering natural variation in root system architecture and growth dynamics using a robotics-assisted phenomics platform
    Therese LaRue, Heike Lindner, Ankit Srinivas, Moisés Expósito‐Alonso, Guillaume Lobet, José R. Dinneny · 2022 · eLife
70. Mucin 1 Gene (MUC1) and Gastric-Cancer Susceptibility
    Norihisa Saeki, Hiromi Sakamoto, Teruhiko Yoshida · 2014 · International Journal of Molecular Sciences
71. Estimating Genetic Effects and Quantifying Missing Heritability Explained by Identified Rare-Variant Associations
    Dajiang J. Liu, Suzanne M. Leal · 2012 · The American Journal of Human Genetics
72. Enrichment of Minor Alleles of Common SNPs and Improved Risk Prediction for Parkinson's Disease
    Zuobin Zhu, Dejian Yuan, Denghui Luo, Xitong Lu, Shi Huang · 2015 · PLoS ONE
73. Genomic inbreeding depression for climatic adaptation of tropical beef cattle
    Antônio Reverter, Laércio R. Porto-Neto, Marina R. S. Fortes, Parthan Kasarapu, María Ángeles Rodríguez de Cara, Heather M. Burrow, Sigrid Arabella Lehnert · 2017 · Journal of Animal Science
74. Comparing miRNA structure of mirtrons and non-mirtrons
    Igor I. Titov, P. S. Vorozheykin · 2018 · BMC Genomics
75. QTL mapping of adult plant and seedling resistance to leaf rust (Puccinia triticina Eriks.) in a multiparent advanced generation intercross (MAGIC) wheat population
    Sandra Rollar, Albrecht Serfling, Manuel Geyer, Lorenz Hartl, Volker Mohler, Frank Ordon · 2020 · Theoretical and Applied Genetics
76. Neurobiological basis for pain vulnerability: why me?
    Franziska Denk, Stephen Brendan McMahon · 2017 · Pain
77. SNPeffect: identifying functional roles of SNPs using metabolic networks
    Debolina Sarkar, Costas D. Maranas · 2020 · The Plant Journal
78. Working Memory Capacities Neurally Dissociate: Evidence from Acute Stroke
    Randi C. Martin, Junhua Ding, A. Cris Hamilton, Tatiana T. Schnur · 2021 · Cerebral Cortex Communications
79. Rocking the foundations of molecular genetics
    John S. Mattick · 2012 · Proceedings of the National Academy of Sciences
80. Prediction of Fetal Hemoglobin in Sickle Cell Anemia Using an Ensemble of Genetic Risk Prediction Models
    Jacqueline N. Milton, Victor R. Gordeuk, James G. Taylor, Mark T. Gladwin, Martin H. Steinberg, Paola Sebastiani · 2014 · Circulation Cardiovascular Genetics
81. From genotype to phenotype inArabidopsis thaliana:in-silicogenome interpretation predicts 288 phenotypes from sequencing data
    Daniele Raimondi, Massimiliano Corso, Piero Fariselli, Yves Moreau · 2021 · Nucleic Acids Research
82. Genetic biomarkers of hypertension and future challenges integrating epigenomics
    Saïd El Shamieh, Sophie Visvikis‐Siest · 2012 · Clinica Chimica Acta
83. Identification of rare variants in Alzheimer’s disease
    Jenny Lord, Alexander J. Lu, Carlos Cruchaga · 2014 · Frontiers in Genetics
84. Pooled Resequencing of 122 Ulcerative Colitis Genes in a Large Dutch Cohort Suggests Population-Specific Associations of Rare Variants in MUC2
    Marijn Caroline Visschedijk, Rudi Alberts, Sören Mucha, Patrick Deelen, Dirk J. de Jong, Marieke J. Pierik, Lieke M. Spekhorst, Floris Imhann, Andrea E. van der Meulen‐de Jong, C. Janneke van der Woude et al. · 2016 · PLoS ONE
85. Heterozygote galactocerebrosidase (GALC) mutants have reduced remyelination and impaired myelin debris clearance following demyelinating injury
    Nicole Scott‐Hewitt, Christopher J. Folts, Jessica M. Hogestyn, Gavin Piester, Margot Mayer-Pröschel, Mark Noble · 2017 · Human Molecular Genetics
86. Bayesian and frequentist analysis of an Austrian genome-wide association study of colorectal cancer and advanced adenomas
    Philipp Hofer, Michael Hagmann, Stefanie Brezina, Erich Dolejsi, Karl Mach, Gernot Leeb, Andreas Baierl, Stephan Buch, Hedwig Sutterlüty, Judith Karner‐Hanusch et al. · 2017 · Oncotarget
87. A joint study of whole exome sequencing and structural MRI analysis in major depressive disorder
    Yamin Zhang, Mingli Li, Qiang Wang, Jacob Shujui Hsu, Wei Deng, Xiaohong Ma, Peiyan Ni, Liansheng Zhao, Yang Tian, Pak Chung Sham et al. · 2019 · Psychological Medicine
88. Structural brain aging and speech production: a surface-based brain morphometry study
    Pascale Tremblay, Isabelle Deschamps · 2015 · Brain Structure and Function
89. Genome-wide association mapping for root cone angle in rice
    Mathilde Bettembourg, Audrey Dardou, Alain Audebert, Emilie Thomas, Julien Frouin, Emmanuel Guiderdoni, Nourollah Ahmadi, Christophe Périn, Anne Diévart, Brigitte Courtois · 2017 · Rice
90. Molecular Origins of Complex Heritability in Natural Genotype-to-Phenotype Relationships
    Christopher M. Jakobson, Daniel F. Jarosz · 2019 · Cell Systems
91. Using extended genealogy to estimate components of heritability for 23 quantitative and dichotomous traits
    Zaitlen, Noah, Kraft, Peter, Patterson, Nick, Pasaniuc, Bogdan, Bhatia, Gaurav, Pollack, Samuela, Price, Alkes L. · 2013 · PLoS Genetics
92. Interplay between Socioeconomic Markers and Polygenic Predisposition on Timing of Dementia Diagnosis
    Olesya Ajnakina, Dorina Cadar, Andrew Steptoe · 2020 · Journal of the American Geriatrics Society
93. Evaluating polygenic risk scores in assessing risk of nine solid and hematologic cancers in European descendants
    Jungyoon Choi, Guochong Jia, Wanqing Wen, Jirong Long, Wei Zheng · 2020 · International Journal of Cancer
94. A missense variant in CST3 exerts a recessive effect on susceptibility to age-related macular degeneration resembling its association with Alzheimer’s disease
    Butler, Joe M., Sharif, Umar, Ali, Manir, McKibbin, Martin, Thompson, Joseph P., Gale, Richard, Yang, Yit C., Inglehearn, Chris, Paraoan, Luminita · 2015 · Human Genetics
95. Natural genetic variation determines susceptibility to aggregation or toxicity in a C. elegansmodel for polyglutamine disease
    Tali Gidalevitz, Ning Wang, Tanuja Deravaj, Jasmine Alexander-Floyd, Richard I. Morimoto · 2013 · BMC Biology
96. Heritability Estimation Approaches Utilizing Genome‐Wide Data
    Amit Kumar Srivastava, Scott M. Williams, Ge Zhang · 2023 · Current Protocols
97. A corollary discharge circuit in human speech
    Amirhossein Khalilian-Gourtani, Ran Wang, Xupeng Chen, Leyao Yu, Patricia C. Dugan, Daniel Friedman, Werner Doyle, Orrin Devinsky, Yao Wang, Adeen Flinker · 2024 · Proceedings of the National Academy of Sciences
98. A map of human microRNA variation uncovers unexpectedly high levels of variability
    José Carbonell‐Caballero, Eva Alloza, Pablo Arce, Salud Borrego, Javier Santoyo‐López, Macarena Ruiz‐Ferrer, Ignacio Medina, Jorge Jimenez-Almazán, Cristina Méndez‐Vidal, María González‐del Pozo et al. · 2012 · Genome Medicine
99. Distinct neural systems recruited when speech production is modulated by different masking sounds
    Sophie Meekings, Samuel Evans, Nadine Lavan, Dana Boebinger, Katya Krieger‐Redwood, Martin P. Cooke, Sophie Kerttu Scott · 2016 · The Journal of the Acoustical Society of America
100. A Model of Compound Heterozygous, Loss-of-Function Alleles Is Broadly Consistent with Observations from Complex-Disease GWAS Datasets
     Jaleal S. Sanjak, Anthony D. Long, Kevin Thornton · 2017 · PLoS Genetics