Ping I Lin

Summary

Publications

  1. ncbi request reprint The mu-opioid receptor polymorphism A118G predicts cortisol responses to naloxone and stress
    Rachel Y Chong
    Department of Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Neuropsychopharmacology 31:204-11. 2006
  2. doi request reprint The WNT2 gene polymorphism associated with speech delay inherent to autism
    Ping I Lin
    Department of Psychiatry, National Taiwan University Hospital, Taipei, Taiwan
    Res Dev Disabil 33:1533-40. 2012
  3. pmc Approaches for unraveling the joint genetic determinants of schizophrenia and bipolar disorder
    Ping I Lin
    Division of Endocrinology, Department of Medicine, University of Maryland School of Medicine, Baltimore, MD, USA
    Schizophr Bull 34:791-7. 2008
  4. doi request reprint Rethinking the genetic basis for comorbidity of schizophrenia and type 2 diabetes
    P I Lin
    Maryland Psychiatric Research Center, University of Maryland School of Medicine, Baltimore, MD, United States
    Schizophr Res 123:234-43. 2010
  5. doi request reprint Association study of the CNS patterning genes and autism in Han Chinese in Taiwan
    Yi Ling Chien
    Department of Psychiatry, National Taiwan University Hospital, Taipei, Taiwan
    Prog Neuropsychopharmacol Biol Psychiatry 35:1512-7. 2011
  6. pmc Assessment of the effect of age at onset on linkage to bipolar disorder: evidence on chromosomes 18p and 21q
    Ping I Lin
    Department of Mental Health, The Bloomberg School of Public Health, The Johns Hopkins University, Baltimore, MD 21205, USA
    Am J Hum Genet 77:545-55. 2005
  7. pmc Runs of homozygosity associated with speech delay in autism in a taiwanese han population: evidence for the recessive model
    Ping I Lin
    Division of Biostatistics and Epidemiology, Cincinnati Children s Hospital Medical Center, Cincinnati, Ohio, United States of America Department of Psychiatry, National Taiwan University Hospital, Taipei, Taiwan
    PLoS ONE 8:e72056. 2013
  8. ncbi request reprint Clinical correlates and familial aggregation of age at onset in bipolar disorder
    Ping I Lin
    Dept of Mental Health, Bloomberg School of Public Health, Johns Hopkins University, 624 N Broadway, 8th Floor, Baltimore, MD 21205, USA
    Am J Psychiatry 163:240-6. 2006
  9. pmc COL4A1 is associated with arterial stiffness by genome-wide association scan
    Kirill V Tarasov
    Laboratory of Cardiovascular Science, Laboratory of Genetics, Clinical Research Branch, Intramural Research Program, National Institute on Aging, National Institutes of Health, Baltimore, MD, USA
    Circ Cardiovasc Genet 2:151-8. 2009
  10. pmc No gene is an island: the flip-flop phenomenon
    Ping I Lin
    Center for Human Genetics, Duke University Medical Center, Durham, NC, USA
    Am J Hum Genet 80:531-8. 2007

Collaborators

Detail Information

Publications12

  1. ncbi request reprint The mu-opioid receptor polymorphism A118G predicts cortisol responses to naloxone and stress
    Rachel Y Chong
    Department of Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Neuropsychopharmacology 31:204-11. 2006
    ..We speculate that increased opioid avidity of the minor allele receptor contributes to the differential response to naloxone vs stress...
  2. doi request reprint The WNT2 gene polymorphism associated with speech delay inherent to autism
    Ping I Lin
    Department of Psychiatry, National Taiwan University Hospital, Taipei, Taiwan
    Res Dev Disabil 33:1533-40. 2012
    ..0012). Therefore, the WNT2 gene may play a suggestive role in language development in autistic disorder. Additionally, the WNT2 gene and EN2 gene may act in concert to influence the language development in autism...
  3. pmc Approaches for unraveling the joint genetic determinants of schizophrenia and bipolar disorder
    Ping I Lin
    Division of Endocrinology, Department of Medicine, University of Maryland School of Medicine, Baltimore, MD, USA
    Schizophr Bull 34:791-7. 2008
    ..We have put a particular emphasis on incorporating the concept of endophenotypes in research of shared genetic liability for these 2 disorders...
  4. doi request reprint Rethinking the genetic basis for comorbidity of schizophrenia and type 2 diabetes
    P I Lin
    Maryland Psychiatric Research Center, University of Maryland School of Medicine, Baltimore, MD, United States
    Schizophr Res 123:234-43. 2010
    ..Hence, endophenotypes of these diseases may be more tractable to identification. To summarize, novel approaches are needed to dissect the complex genetic basis of the comorbidity of SCZ and T2D...
  5. doi request reprint Association study of the CNS patterning genes and autism in Han Chinese in Taiwan
    Yi Ling Chien
    Department of Psychiatry, National Taiwan University Hospital, Taipei, Taiwan
    Prog Neuropsychopharmacol Biol Psychiatry 35:1512-7. 2011
    ..A haplotype of WNT2 (rs2896218-rs6950765: G-G) is significantly associated with ASDs in our trios samples, this finding warrants further validation by different sample and confirmation by functional study...
  6. pmc Assessment of the effect of age at onset on linkage to bipolar disorder: evidence on chromosomes 18p and 21q
    Ping I Lin
    Department of Mental Health, The Bloomberg School of Public Health, The Johns Hopkins University, Baltimore, MD 21205, USA
    Am J Hum Genet 77:545-55. 2005
    ..This inconsistency may be due to differences in the AAO characteristics of the samples examined. Future studies to fine map susceptibility genes for BP on chromosomes 21q22.13 and 18p11.2 should take AAO into account...
  7. pmc Runs of homozygosity associated with speech delay in autism in a taiwanese han population: evidence for the recessive model
    Ping I Lin
    Division of Biostatistics and Epidemiology, Cincinnati Children s Hospital Medical Center, Cincinnati, Ohio, United States of America Department of Psychiatry, National Taiwan University Hospital, Taipei, Taiwan
    PLoS ONE 8:e72056. 2013
    ..3 may play a role in language impairment in autism. More research is warranted to investigate if these genes influence speech pathology by perturbing cerebellar functions. ..
  8. ncbi request reprint Clinical correlates and familial aggregation of age at onset in bipolar disorder
    Ping I Lin
    Dept of Mental Health, Bloomberg School of Public Health, Johns Hopkins University, 624 N Broadway, 8th Floor, Baltimore, MD 21205, USA
    Am J Psychiatry 163:240-6. 2006
    ....
  9. pmc COL4A1 is associated with arterial stiffness by genome-wide association scan
    Kirill V Tarasov
    Laboratory of Cardiovascular Science, Laboratory of Genetics, Clinical Research Branch, Intramural Research Program, National Institute on Aging, National Institutes of Health, Baltimore, MD, USA
    Circ Cardiovasc Genet 2:151-8. 2009
    ..Heritability and linkage studies have pointed toward a genetic component affecting PWV. We conducted a genome-wide association study to identify single-nucleotide polymorphisms (SNPs) associated with PWV...
  10. pmc No gene is an island: the flip-flop phenomenon
    Ping I Lin
    Center for Human Genetics, Duke University Medical Center, Durham, NC, USA
    Am J Hum Genet 80:531-8. 2007
    ....
  11. ncbi request reprint Parsing the genetic heterogeneity of chromosome 12q susceptibility genes for Alzheimer disease by family-based association analysis
    Ping I Lin
    Center for Human Genetics, Duke University Medical Center, Durham, NC, USA
    Neurogenetics 7:157-65. 2006
    ..0026). These results suggest that subset and covariate analyses may be one approach to help identify novel susceptibility genes on chromosome 12q for LOAD...
  12. pmc Revealing the role of glutathione S-transferase omega in age-at-onset of Alzheimer and Parkinson diseases
    Yi Ju Li
    Department of Medicine and Center for Human Genetics, Duke University Medical Center, Box 3445, Durham, NC 27710, USA
    Neurobiol Aging 27:1087-93. 2006
    ..These findings suggest the presence of genetic heterogeneity for GSTO1h's effect on AAO, and support GSTO1h's role in modifying AAO in these two disorders...