Whole-Genome Sequencing in a Patient with Charcot–Marie–Tooth Neuropathy

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  1. Association of Candidate Genes with Phenotypic Traits Relevant to Anorexia Nervosa
    Tammy L. Root, Jin Peng Szatkiewicz, Charles Richard Jonassaint, Laura M. Thornton, Andréa Poyastro Pinheiro, Michael A. Strober, Cinnamon S. Bloss, Wade H. Berrettini, Nicholas J. Schork, Walter H. Kaye et al. · 2011 · European Eating Disorders Review
  2. The genetics of common kidney disease: a pathway toward clinical relevance
    Paul E. Drawz, John R. Sedor · 2011 · Nature Reviews Nephrology
  3. Likelihood ratios for genome medicine
    Alexander A. Morgan, Rong Chen, Atul Janardhan Butte · 2010 · Genome Medicine
  4. Clinical utility of whole-exome sequencing in rare diseases: Galactosialidosis
    Prada, Carlos E., Gonzaga-Jauregui, Claudia, Tannenbaum, Rebecca, Penney, Samantha, Lupski, James R., Hopkin, Robert J., Sutton, V. Reid · 2014 · European Journal of Medical Genetics
  5. Haplotype-specific modulation of a SOX10/CREB response element at the Charcot–Marie–Tooth disease type 4C locus SH3TC2
    Megan Hwa Brewer, Ki Hwan Ma, Gary W. Beecham, Chetna Gopinath, Frank Baas, Byung‐Ok Choi, Mary M. Reilly, Michael E. Shy, Stephan L. Zuchner, John P. Svaren et al. · 2014 · Human Molecular Genetics
  6. Clinical and histopathological study of Charcot-Marie-Tooth neuropathy with a novel S90W mutation in BSCL2
    B.-O. Choi, M.-H. Park, K. W. Chung, Hae-Mi Woo, H. Koo, H. Chung, Kyu-Ryong Choi, K. Park, Hye-Jin Lee, Y. S. Hyun et al. · 2012 · Neurogenetics
  7. Sensitive and fast mapping of di-base encoded reads
    Farhad Hormozdiari, Faraz Hach, S. Cenk Şahinalp, Evan E. Eichler, Can Alkan · 2011 · Bioinformatics
  8. Genome Medicine: past, present and future
    Charles Auffray, Timothy Caulfield, Muin J. Khoury, James R. Lupski, Matthias Georg Schwab, Timothy D. Veenstra · 2011 · Genome Medicine
  9. Sperm and testis mediated DNA transfer as a means of gene therapy
    J. Parrington, K. Coward, J. Gadea · 2011 · Systems Biology in Reproductive Medicine
  10. Investigative pathology: leading the post-genomic revolution
    David Monty Berman, Marcus Bosenberg, Robin Orwant, Beth L. Thurberg, Giulio Francesco Draetta, Christopher D.�M. Fletcher, Massimo F. Loda · 2011 · Laboratory Investigation
  11. Diagnostic yield of clinical exome sequencing as a first-tier genetic test for the diagnosis of genetic disorders in pediatric patients: results from a referral center study
    Jean-Philippe Mergnac, Arnaud Wiedemann, Céline Chéry, Jean‐Marie Ravel, Farès Namour, Jean‐Louis Guéant, François Feillet, Abderrahim Oussalah · 2021 · Human Genetics
  12. Clan genomics: From OMIM phenotypic traits to genes and biology
    James R. Lupski · 2021 · American Journal of Medical Genetics Part A
  13. Early-Onset Progressive Retinal Atrophy Associated with an IQCB1 Variant in African Black-Footed Cats (Felis nigripes)
    Annie Oh, Jacqueline W. Pearce, Barbara Gandolfi, Erica K. Creighton, William Kirk Suedmeyer, Michael Selig, Ann P. Bosiack, Leilani J. Castaner, Rebecca E.H. Whiting, Ellen B. Belknap et al. · 2017 · Scientific Reports
  14. Integrating population variation and protein structural analysis to improve clinical interpretation of missense variation: application to the WD40 domain
    Roman A. Laskowski, Nidhi Tyagi, Diana S. Johnson, Shelagh K. Joss, Esther Kinning, Catherine McWilliam, Miranda P. Splitt, Janet M. Thornton, Helen V. Firth, the DDD Study et al. · 2016 · Human Molecular Genetics
  15. Whole genome sequencing as a means to assess pathogenic mutations in medical genetics and cancer
    Béryl Royer‐Bertrand, Carlo Rivolta · 2014 · Cellular and Molecular Life Sciences
  16. Delivery of a Clinical Genomics Service
    William G. Newman, Graeme Charles M. Black · 2014 · Genes
  17. Overview of the Development of Personalized Genomic Medicine and Surgery
    Francis Charles Brunicardi, Richard A. Gibbs, David A. Wheeler, John J. Nemunaitis, William P. Fisher, John A. Goss, Changyi Chen · 2011 · World Journal of Surgery
  18. Genome-wide association studies of sleep disorders.
    D. Raizen, Mark N. Wu · 2011 · Chest
  19. The Genetics of Alzheimer's Disease
    Lars Bertram, Rudolph E. Tanzi · 2012 · Progress in molecular biology and translational science
  20. Identifying PD-causing genes and genetic susceptibility factors
    Thomas Gasser · 2010 · Progress in brain research
  21. Exclusive expression of the Rab11 effector SH3TC2 in Schwann cells links integrin-α6 and myelin maintenance to Charcot-Marie-Tooth disease type 4C
    Sauparnika Vijay, Meagan Chiu, Joel B. Dacks, Rhys C. Roberts · 2016 · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
  22. Association of CDH11 with non‐syndromic ASD
    An Crepel, Veerle De Wolf, Nathalie Brison, Berten Ceulemans, Didier Walleghem, Gilian Peuteman, Diether Lambrechts, Jean G. Steyaert, Ilse L. J. Noens, Koenraad Devriendt et al. · 2014 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
  23. Whole‐Exome Sequencing Reveals GPIHBP1 Mutations in Infantile Colitis With Severe Hypertriglyceridemia
    Claudia G. Gonzaga-Jauregui, Sabina A. V. Mir, Samantha Penney, Shalini N. Jhangiani, Craig Midgen, Milton J. Finegold, Donna Marie Muzny, Min Wang, Carlos A. Bacino, Richard A. Gibbs et al. · 2014 · Journal of Pediatric Gastroenterology and Nutrition
  24. Exome sequencing identification of a GJB1 missense mutation in a kindred with X-linked spinocerebellar ataxia (SCA-X1).
    M. Caramins, J. Colebatch, M. Bainbridge, S. Scherer, C. Abrams, E. Hackett, M. Freidin, S. Jhangiani, Min Wang, Yuan-Qing Wu et al. · 2013 · Human Molecular Genetics
  25. Estimation of Copy Number Alterations from Exome Sequencing Data
    Rafael Valdés‐Mas, Sı́lvia Beà, Diana A. Puente, Carlos López-Otı́n, Xosé S. Puente · 2012 · PLoS ONE
  26. A mild form of Mucopolysaccharidosis IIIB diagnosed with targeted next-generation sequencing of linked genomic regions
    K. Selmer, G. Gilfillan, P. Strømme, R. Lyle, T. Hughes, H. Hjorthaug, K. Brandal, S. Nakken, D. Misceo, T. Egeland et al. · 2011 · European Journal of Human Genetics
  27. Genetic regulation of human brain development: lessons from Mendelian diseases
    Tracy Dixon‐Salazar, Joseph G. Gleeson · 2010 · Annals of the New York Academy of Sciences
  28. Microdeletion and Microduplication Syndromes
    Lisenka E.L.M. Vissers, Paweł Stankiewicz · 2011 · Methods in molecular biology
  29. Mutations in COMP cause familial carpal tunnel syndrome
    Chunyu Li, Ni Wang, Alejandro A. Schäffer, Xilin Liu, Zhuo Zhao, Gene Elliott, Lisa J Garrett, Nga Ting Choi, Yueshu Wang, Yufa Wang et al. · 2020 · Nature Communications
  30. Phenotype-Driven Virtual Panel Is an Effective Method to Analyze WES Data of Neurological Disease
    Xu Wang, Xiang Shen, F. Fang, Chang-Hong Ding, H. Zhang, Zhen-Fei Cao, Dong An · 2019 · Frontiers in Pharmacology
  31. Rare variants in known and novel candidate genes predisposing to statin-associated myopathy.
    M. Neroldova, V. Stránecký, K. Hodaňová, H. Hartmannová, L. Piherová, A. Přistoupilová, L. Mrázová, M. Vrablík, V. Adámková, J. Hubáček et al. · 2016 · Pharmacogenomics (London)
  32. Sequence to Medical Phenotypes: A Framework for Interpretation of Human Whole Genome DNA Sequence Data
    Frederick E. Dewey, Megan E. Grove, James Rush Priest, Daryl M. Waggott, Prag Batra, Clint L. Miller, Matthew Thomas Wheeler, Amin Zia, Cuiping Pan, Konrad J. Karczewski et al. · 2015 · PLoS Genetics
  33. Genome, Exome, and Targeted Next-Generation Sequencing in Neonatal Diabetes
    Elisa De Franco, Sian Ellard · 2015 · Pediatric Clinics of North America
  34. The foot and ankle examination.
    Dean N. Papaliodis, Maria Vanushkina, Nicholas Richardson, John A. Dipreta · 2014 · The Medical clinics of North America
  35. Perspectives on Clinical Informatics: Integrating Large-Scale Clinical, Genomic, and Health Information for Clinical Care
    I. Choi, Tae-Min Kim, M. Kim, S. Mun, Y. Chung · 2013 · Genomics & Informatics
  36. Developments in Molecular Genetic Diagnostics: An Update for the Pediatric Epilepsy Specialist
    Amanda W. Pong, Deb K. Pal, Wendy K. Chung · 2011 · Pediatric Neurology
  37. Biology in balance: human diploid genome integrity, gene dosage, and genomic medicine
    J. Lupski · 2022 · Trends in Genetics
  38. Current scenario of the genetic testing for rare neurological disorders exploiting next generation sequencing
    Chiara Di Resta, Giovanni Battista Pipitone, Paola Carrera, Maurizio Ferrari · 2020 · Neural Regeneration Research
  39. Comparison and evaluation of two exome capture kits and sequencing platforms for variant calling
    Guoqiang Zhang, Jianfeng Wang, Jin Yang, Wenjie Li, Yutian Deng, Jing Li, Jun T. Huang, Songnian Hu, Bing Zhang · 2015 · BMC Genomics
  40. Prioritizing Disease-Linked Variants, Genes, and Pathways with an Interactive Whole-Genome Analysis Pipeline
    In‐Hee Lee, Kyungjoon Lee, Michael Hsing, Yongjoon Choe, Jin‐Ho Park, Shu Hee Kim, Justin M. Bohn, Matthew B. Neu, Kyu‐Baek Hwang, Robert C. Green et al. · 2014 · Human Mutation
  41. A practical approach to molecular diagnostic testing in neuromuscular diseases.
    W. Arnold, K. Flanigan · 2012 · Physical Medicine and Rehabilitation Clinics of North America
  42. Chromosome microarray in Australia: A guide for paediatricians
    E. Palmer, Greg B. Peters, D. Mowat · 2012 · Journal of Paediatrics and Child Health
  43. Cell autonomous and systemic factors in progeria development
    Fernando G. Osorio, Alejandro Pineiro Ugalde, Guillermo Mariño, Xosé S. Puente, José M.P. Freije, Carlos López-Otı́n · 2011 · Biochemical Society Transactions
  44. Consanguinity Mapping of Congenital Heart Disease in a South Indian Population
    Tracy L. Mcgregor, A. Misri, J. Bartlett, G. Orabona, Richard D. Friedman, D. Sexton, S. Maheshwari, T. M. Morgan · 2010 · PLoS ONE
  45. Identification of genetic association of multiple rare variants using collapsing methods
    Yan V. Sun, Yun Ju Sung, Nathan Tintle, Andreas Ziegler · 2011 · Genetic Epidemiology
  46. A comparative study of k-spectrum-based error correction methods for next-generation sequencing data analysis
    Isaac Akogwu, Nan Wang, Chaoyang Zhang, Ping Gong · 2016 · Human Genomics
  47. Bioinformatics Workflow for Clinical Whole Genome Sequencing at Partners HealthCare Personalized Medicine
    Ellen A. Tsai, Rimma Shakbatyan, J. Evans, Peter Rossetti, Chet Graham, Himanshu Sharma, Chiao-Feng Lin, Matthew S. Lebo · 2016 · Journal of Personalized Medicine
  48. Next generation sequencing and rare genetic variants: From human population studies to medical genetics
    Giuseppe Matullo, Cornelia Di Gaetano, Simonetta Guarrera · 2013 · Environmental and Molecular Mutagenesis
  49. Molecular analysis of the genes causing recessive demyelinating Charcot–Marie–Tooth disease in Japan
    M. Hayashi, A. Abe, Tatsufumi Murakami, S. Yamao, H. Arai, H. Hattori, M. Iai, Kyoko Watanabe, N. Oka, K. Chida et al. · 2013 · Journal of Human Genetics
  50. The Business Value and Cost–effectiveness of Genomic Medicine
    James M. Crawford, Mara G. Aspinall · 2012 · Personalized Medicine
  51. [Guidelines for molecular diagnosis of Charcot-Marie-Tooth disease].
    J. Berciano, T. Sevilla, C. Casasnovas, R. Sivera, J. Vílchez, Jon Infante, C. Ramón, A. Pelayo-Negro, I. Illa · 2012
  52. Schwann Cell and the Pathogenesis of Charcot-Marie-Tooth Disease.
    Tatsufumi Murakami, Y. Sunada · 2019 · Advances in Experimental Medicine and Biology
  53. Application of high-throughput sequencing for studying genomic variations in congenital heart disease
    C. Dorn, Marcel Grunert, Silke Sperling · 2013 · Briefings in Functional Genomics
  54. Rapid Whole-Genome Sequencing in Critically Ill Infants and Children with Suspected, Undiagnosed Genetic Diseases: Evolution to a First-Tier Clinical Laboratory Test in the Era of Precision Medicine
    Rina Kansal · 2025 · Children
  55. Secondary findings: How did we get here, and where are we going?
    K. Ormond, Julianne M. O'Daniel, Sarah S. Kalia · 2019 · Journal of Genetic Counseling
  56. Effective Variant Detection by Targeted Deep Sequencing of DNA Pools: An Example from Parkinson's Disease
    Lasse Pihlstrøm, Aina Haugen Rengmark, Kari Anne Bjørnarå, Mathias Toft · 2014 · Annals of Human Genetics
  57. How novel molecular diagnostic technologies and biomarkers are revolutionizing genetic testing and patient care
    Linnea M. Baudhuin, Leslie J. Donato, Timothy S. Uphoff · 2011 · Expert Review of Molecular Diagnostics
  58. Fanconi's anemia in adulthood: chemoradiation-induced bone marrow failure and a novel FANCA mutation identified by targeted deep sequencing.
    I. Tan, I. Cutcutache, Z. Zang, J. Iqbal, S. Yap, W. Hwang, W. Lim, B. Teh, S. Rozen, E. Tan et al. · 2011 · Journal of Clinical Oncology
  59. Genomic medicine and neurological disease
    Philip M. Boone, Wojciech K. Wiszniewski, James R. Lupski · 2011 · Human Genetics
  60. Reliable resequencing of the human dystrophin locus by universal long polymerase chain reaction and massive pyrosequencing
    Raoul J.P. Bonnal, Marco Severgnini, Alessandra Castaldi, Roberta Bordoni, Michele Iacono, Amelia Trimarco, Annalaura Torella, Giulio Piluso, Stefania Aurino, Gianluigi Condorelli et al. · 2010 · Analytical Biochemistry
  61. Exome Sequencing Analysis: A Guide to Disease Variant Detection
    Ofer Isakov, Marie E. Perrone, Noam Shomron · 2013 · Methods in molecular biology
  62. Quantitative dissection of multilocus pathogenic variation in an Egyptian infant with severe neurodevelopmental disorder resulting from multiple molecular diagnoses
    I. Herman, Angad Jolly, Hao-Wei Du, Moez Dawood, G. Abdel-Salam, D. Marafi, T. Mitani, D. Calame, Z. Coban-Akdemir, J. Fatih et al. · 2021 · American Journal of Medical Genetics. Part A
  63. Charcot–Marie–Tooth Disease type 4C: Novel mutations, clinical presentations, and diagnostic challenges
    Nivedita U. Jerath, Ami K. Mankodi, Thomas O. Crawford, Christopher Grunseich, Hasna Baloui, Chioma Nnamdi‐Emeratom, Alice B. Schindler, Terry D Heiman-Patterson, Roman Chrast, Michael E. Shy · 2017 · Muscle & Nerve
  64. Diagnostic use of Massively Parallel Sequencing in Neuromuscular Diseases: Towards an Integrated Diagnosis
    V. Biancalana, J. Laporte · 2015 · Journal of Neuromuscular Diseases
  65. Technological advances in DNA sequence enrichment and sequencing for germline genetic diagnosis
    Chee‐Seng Ku, Mengchu Wu, D.N. Cooper, Nasheen Naidoo, Yudi Pawitan Y, Brendan Pang, Barry J. Iacopetta, Richie Soong · 2012 · Expert Review of Molecular Diagnostics
  66. Annotating individual human genomes
    Ali Torkamani, Ashley A. Scott‐Van Zeeland, Eric J. Topol, Nicholas J. Schork · 2011 · Genomics
  67. Genetic testing for autism: recent advances and clinical implications
    David T. Miller · 2010 · Expert Review of Molecular Diagnostics
  68. De Novo and Inherited Variants in GBF1 are Associated with Axonal Neuropathy Caused by Golgi Fragmentation
    Natalia Mendoza-Ferreira, Mert Karakaya, Nur Cengiz, D. Beijer, K. Brigatti, C. Gonzaga-Jauregui, N. Fuhrmann, Irmgard Hölker, M. P. Thelen, S. Zetzsche et al. · 2020 · American Journal of Human Genetics
  69. Evaluating Rare Variants in Complex Disorders Using Next-Generation Sequencing
    Matthew N. Ezewudo, Michael E. Zwick · 2013 · Current Psychiatry Reports
  70. Genomic medicine enters the neurology clinic
    G. Coppola, D. Geschwind · 2012 · Neurology
  71. Single Nucleotide Polymorphism (SNP) Detection and Genotype Calling from Massively Parallel Sequencing (MPS) Data
    Yun Li, Wei Chen, Eric Yi Liu, Yi‐Hui Zhou · 2012 · Statistics in Biosciences
  72. Identification of Variants in CNGA3 as Cause for Achromatopsia by Exome Sequencing of a Single Patient
    Kevin Lam · 2011 · Archives of Ophthalmology
  73. Impact of Mendelian inheritance in cardiovascular disease
    Kim L. McBride, Vidu Garg · 2010 · Annals of the New York Academy of Sciences
  74. Next generation sequencing methodologies--an overview.
    W. Pickrell, M. Rees, S. Chung · 2012 · Advances in Protein Chemistry and Structural Biology
  75. Genetics of inherited peripheral neuropathies and the next frontier: looking backwards to progress forwards
    J. Parmar, Nigel G. Laing, Marina L. Kennerson, Gianina Ravenscroft · 2024 · Journal of Neurology Neurosurgery & Psychiatry
  76. Discovery of genomic variation across a generation
    Brett Trost, Livia Oliveira Loureiro, Stephen W. Scherer · 2021 · Human Molecular Genetics
  77. DeviCNV: detection and visualization of exon-level copy number variants in targeted next-generation sequencing data
    Yeeok Kang, Seong-Hyeuk Nam, Kyung Park, Yoonjung Kim, Jong‐Won Kim, Eunjung Lee, Jung Min Ko, Kyung‐A Lee, In Ho Park · 2018 · BMC Bioinformatics
  78. IRF2BPL Is Associated with Neurological Phenotypes
    Paul C. Marcogliese, Vandana Shashi, Rebecca C. Spillmann, Nicholas Stong, Jill Anne Rosenfeld, Mary Kay Koenig, Julián A. Martínez-Agosto, Matthew R. Herzog, Agnes H. Chen, Patricia Dickson et al. · 2018 · The American Journal of Human Genetics
  79. Clinical genomics: from a truly personal genome viewpoint
    James R. Lupski · 2016 · Human Genetics
  80. Phasing for medical sequencing using rare variants and large haplotype reference panels
    Kevin Sharp, Warren W. Kretzschmar, Olivier Delaneau, Jonathan Marchini · 2016 · Bioinformatics
  81. Focus group discussions on secondary variants and next-generation sequencing technologies.
    Gabrielle M. Christenhusz, K. Devriendt, H. van Esch, K. Dierickx · 2015 · European Journal of Medical Genetics
  82. Genetic Investigation of Bisphosphonate-Related Osteonecrosis of Jaw (BRONJ) via Whole Exome Sequencing and Bioinformatics
    Jee-Hwan Kim, Yong Jae Ko, Ji-Young Kim, Y. Oh, Jihye Hwang, S. Han, Sanguk Kim, Jae-Hoon Lee, Dong-Hoo Han · 2015 · PLoS ONE
  83. Obstacles and opportunities for the future of genomic medicine
    B. Solomon · 2014 · Molecular Genetics & Genomic Medicine
  84. Genomic analysis of the blood attributed to Louis XVI (1754–1793), king of France
    Íñigo Olalde, Federico Sánchez‐Quinto, Debayan Datta, Urko M. Marigorta, Charleston W. K. Chiang, Juan Antonio Rodríguez, Marcos Fernández-Callejo, Irene González, Magda Montfort, Laura Matas-Lalueza et al. · 2014 · Scientific Reports
  85. A Proposed Clinical Decision Support Architecture Capable of Supporting Whole Genome Sequence Information
    Brandon M. Welch, S. Loya, K. Eilbeck, Kensaku Kawamoto · 2014 · Journal of Personalized Medicine
  86. [Guidelines for molecular diagnosis of Charcot-Marie-Tooth disease].
    J. Berciano, T. Sevilla, C. Casasnovas, R. Sivera, J. J. Vílchez, J. Infante, C. Ramón, Ana L. Pelayo-Negro, I. Illa · 2012 · Neurología
  87. Inherited glomerular diseases
    M. Rheault, C. Kashtan · 2012 · Springer eBooks
  88. Aquila enables reference-assisted diploid personal genome assembly and comprehensive variant detection based on linked reads
    Xin Zhou, Lu Zhang, Z. Weng, D. Dill, A. Sidow · 2021 · Nature Communications
  89. Inferring biosynthetic and gene regulatory networks from Artemisia annua RNA sequencing data on a credit card-sized ARM computer
    Qiao Tan, M. Mutwil · 2019 · bioRxiv
  90. Germline susceptibility variants impact clinical outcome and therapeutic strategies for stage III colorectal cancer
    Peng‐Chan Lin, Yu‐Min Yeh, Pei‐Ying Wu, Keng‐Fu Hsu, Jang‐Yang Chang, Meng‐Ru Shen · 2019 · Scientific Reports
  91. From genes to genomes in the clinic
    Joris A. Veltman, James R. Lupski · 2015 · Genome Medicine
  92. Integrating precision medicine in the study and clinical treatment of a severely mentally ill person
    Jason O'Rawe, Han Fang, Shawn G. Rynearson, Reid J. Robison, Edward S. Kiruluta, Gerald A. Higgins, Karen L Eilbeck, Martin G. Reese, Gholson J. Lyon · 2013 · PeerJ
  93. Next-generation sequencing diagnostics for neurological diseases/disorders: from a clinical perspective
    Jia Nee Foo, Jianjun Liu, Eng‐King Tan · 2013 · Human Genetics
  94. Future possibilities in migraine genetics
    Laura Aviaja Rudkjøbing, Ann-Louise Esserlind, J. Olesen · 2012 · The Journal of Headache and Pain
  95. Hereditary Hearing Loss: Genetic Counselling
    Rubén Cabanillas Farpón, J. Bañales · 2012
  96. Exome sequencing in children with clinically suspected maturity‐onset diabetes of the young
    Mustafa Tosur, Claudia Soler‐Alfonso, Katie M. Chan, Michael M. Khayat, Shalini N. Jhangiani, Qingchang Meng, AHMAD K. REFAEY, Donna Marie Muzny, Richard A. Gibbs, David R. Murdock et al. · 2021 · Pediatric Diabetes
  97. New Technologies for Monitoring Marine Mammal Health
    Annalaura Mancia · 2018 · Elsevier eBooks
  98. Inheritance-mode specific pathogenicity prioritization (ISPP) for human protein coding genes
    Jacob Shujui Hsu, Johnny S. H. Kwan, Zhicheng Pan, María-Mercé García-Barceló, Pak Chung Sham, Miaoxin Li · 2016 · Bioinformatics
  99. Endophenotypes as a measure of suicidality
    Dimitry A. Chistiakov, Zurab I. Kekelidze, Vladimir Pavlovich Chekhonin · 2012 · Journal of Applied Genetics
  100. Whole genome sequencing identifies causal variants in CMT
    Stephan L. Zuchner · 2010 · Nature Reviews Neurology