Lauren Weiss, PhD - Publications

Affiliations: 
Psychiatry University of California, San Francisco, San Francisco, CA 
Area:
Genetics of Autism

41 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any innacuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2018 Bizaoui V, Gage J, Brar R, Rauen KA, Weiss LA. RASopathies are associated with a distinct personality profile. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 29659143 DOI: 10.1002/ajmg.b.32632  0.6
2018 Young O, Perati S, Weiss LA, Rauen KA. Age and ASD symptoms in Costello syndrome. American Journal of Medical Genetics. Part A. 176: 1027-1028. PMID 29575620 DOI: 10.1002/ajmg.a.38641  0.6
2017 Deshpande A, Yadav S, Dao DQ, Wu ZY, Hokanson KC, Cahill MK, Wiita AP, Jan YN, Ullian EM, Weiss LA. Cellular Phenotypes in Human iPSC-Derived Neurons from a Genetic Model of Autism Spectrum Disorder. Cell Reports. 21: 2678-2687. PMID 29212016 DOI: 10.1016/j.celrep.2017.11.037  0.6
2017 Mitra I, Lavillaureix A, Yeh E, Traglia M, Tsang K, Bearden CE, Rauen KA, Weiss LA. Reverse Pathway Genetic Approach Identifies Epistasis in Autism Spectrum Disorders. Plos Genetics. 13: e1006516. PMID 28076348 DOI: 10.1371/journal.pgen.1006516  0.6
2016 Josowitz R, Mulero-Navarro S, Rodriguez NA, Falce C, Cohen N, Ullian EM, Weiss LA, Rauen KA, Sobie EA, Gelb BD. Autonomous and Non-autonomous Defects Underlie Hypertrophic Cardiomyopathy in BRAF-Mutant hiPSC-Derived Cardiomyocytes. Stem Cell Reports. PMID 27569062 DOI: 10.1016/j.stemcr.2016.07.018  0.6
2016 Rooney GE, Goodwin AF, Depeille P, Sharir A, Schofield CM, Yeh E, Roose JP, Klein OD, Rauen KA, Weiss LA, Ullian EM. Human iPS Cell-Derived Neurons Uncover the Impact of Increased Ras Signaling in Costello Syndrome. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 36: 142-52. PMID 26740656 DOI: 10.1523/JNEUROSCI.1547-15.2016  0.6
2015 Krencik R, Hokanson KC, Narayan AR, Dvornik J, Rooney GE, Rauen KA, Weiss LA, Rowitch DH, Ullian EM. Dysregulation of astrocyte extracellular signaling in Costello syndrome. Science Translational Medicine. 7: 286ra66. PMID 25947161 DOI: 10.1126/scitranslmed.aaa5645  0.6
2015 Desachy G, Croen LA, Torres AR, Kharrazi M, Delorenze GN, Windham GC, Yoshida CK, Weiss LA. Increased female autosomal burden of rare copy number variants in human populations and in autism families. Molecular Psychiatry. 20: 170-5. PMID 25582617 DOI: 10.1038/mp.2014.179  0.6
2014 De Rubeis S, He X, Goldberg AP, Poultney CS, Samocha K, Cicek AE, Kou Y, Liu L, Fromer M, Walker S, Singh T, Klei L, Kosmicki J, Shih-Chen F, Aleksic B, ... ... Weiss LA, et al. Synaptic, transcriptional and chromatin genes disrupted in autism. Nature. 515: 209-15. PMID 25363760 DOI: 10.1038/nature13772  0.6
2014 Bershteyn M, Hayashi Y, Desachy G, Hsiao EC, Sami S, Tsang KM, Weiss LA, Kriegstein AR, Yamanaka S, Wynshaw-Boris A. Cell-autonomous correction of ring chromosomes in human induced pluripotent stem cells. Nature. 507: 99-103. PMID 24413397 DOI: 10.1038/nature12923  0.6
2014 Adviento B, Corbin IL, Widjaja F, Desachy G, Enrique N, Rosser T, Risi S, Marco EJ, Hendren RL, Bearden CE, Rauen KA, Weiss LA. Autism traits in the RASopathies. Journal of Medical Genetics. 51: 10-20. PMID 24101678 DOI: 10.1136/jmedgenet-2013-101951  0.6
2013 Tsang KM, Croen LA, Torres AR, Kharrazi M, Delorenze GN, Windham GC, Yoshida CK, Zerbo O, Weiss LA. A genome-wide survey of transgenerational genetic effects in autism. Plos One. 8: e76978. PMID 24204716 DOI: 10.1371/journal.pone.0076978  0.6
2013 Abrahams BS, Arking DE, Campbell DB, Mefford HC, Morrow EM, Weiss LA, Menashe I, Wadkins T, Banerjee-Basu S, Packer A. SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs). Molecular Autism. 4: 36. PMID 24090431 DOI: 10.1186/2040-2392-4-36  0.6
2013 Martin PM, Yang X, Robin N, Lam E, Rabinowitz JS, Erdman CA, Quinn J, Weiss LA, Hamilton SP, Kwok PY, Moon RT, Cheyette BN. A rare WNT1 missense variant overrepresented in ASD leads to increased Wnt signal pathway activation. Translational Psychiatry. 3: e301. PMID 24002087 DOI: 10.1038/tp.2013.75  0.6
2013 Weiss LA, Chambers CD. Associations between multivitamin supplement use and alcohol consumption before pregnancy: Pregnancy Risk Assessment Monitoring System, 2004 to 2008. Alcoholism, Clinical and Experimental Research. 37: 1595-600. PMID 23906504 DOI: 10.1111/acer.12120  0.6
2013 Jones KL, Weiss LA, Hagey LR, Gonzalez V, Benirschke K, Chambers CD. Altered lipid metabolism in gastroschisis: a novel hypothesis. American Journal of Medical Genetics. Part A. 161: 1860-5. PMID 23794282 DOI: 10.1002/ajmg.a.36002  0.6
2013 Cheng Y, Quinn JF, Weiss LA. An eQTL mapping approach reveals that rare variants in the SEMA5A regulatory network impact autism risk. Human Molecular Genetics. 22: 2960-72. PMID 23575222 DOI: 10.1093/hmg/ddt150  0.6
2013 Goodwin AF, Oberoi S, Landan M, Charles C, Groth J, Martinez A, Fairley C, Weiss LA, Tidyman WE, Klein OD, Rauen KA. Craniofacial and dental development in cardio-facio-cutaneous syndrome: the importance of Ras signaling homeostasis. Clinical Genetics. 83: 539-44. PMID 22946697 DOI: 10.1111/cge.12005  0.6
2012 Chow ML, Pramparo T, Winn ME, Barnes CC, Li HR, Weiss L, Fan JB, Murray S, April C, Belinson H, Fu XD, Wynshaw-Boris A, Schork NJ, Courchesne E. Age-dependent brain gene expression and copy number anomalies in autism suggest distinct pathological processes at young versus mature ages. Plos Genetics. 8: e1002592. PMID 22457638 DOI: 10.1371/journal.pgen.1002592  0.6
2012 Weiss LA, Chambers CD, Gonzalez V, Hagey LR, Jones KL. The omega-6 fatty acid linoleic acid is associated with risk of gastroschisis: a novel dietary risk factor. American Journal of Medical Genetics. Part A. 158: 803-7. PMID 22315197 DOI: 10.1002/ajmg.a.35204  0.6
2009 Weiss LA. Autism genetics: emerging data from genome-wide copy-number and single nucleotide polymorphism scans. Expert Review of Molecular Diagnostics. 9: 795-803. PMID 19895225 DOI: 10.1586/erm.09.59  0.6
2009 Weiss LA, Arking DE, Daly MJ, Chakravarti A, Brune CW, West K, O'Connor A, Hilton G, Tomlinson RL, West AB, Cook EH, Green T, Chang SC, Gabriel S, Gates C, et al. A genome-wide linkage and association scan reveals novel loci for autism Nature. 461: 802-808. PMID 19812673 DOI: 10.1038/nature08490  0.6
2009 Weiss LA. New insights into genomic variation in health and disease. Genome Medicine. 1: 41. PMID 19435489 DOI: 10.1186/gm41  0.6
2009 Blaya C, Moorjani P, Salum GA, Gonçalves L, Weiss LA, Leistner-Segal S, Manfro GG, Smoller JW. Preliminary evidence of association between EFHC2, a gene implicated in fear recognition, and harm avoidance. Neuroscience Letters. 452: 84-6. PMID 19429002 DOI: 10.1016/j.neulet.2009.01.036  0.6
2009 McCarthy JJ, Somji A, Weiss LA, Steffy B, Vega R, Barrett-Connor E, Talavera G, Glynne R. Polymorphisms of the scavenger receptor class B member 1 are associated with insulin resistance with evidence of gene by sex interaction. The Journal of Clinical Endocrinology and Metabolism. 94: 1789-96. PMID 19276229 DOI: 10.1210/jc.2008-2800  0.6
2008 Weiss LA, Shen Y, Korn JM, Arking DE, Miller DT, Fossdal R, Saemundsen E, Stefansson H, Ferreira MA, Green T, Platt OS, Ruderfer DM, Walsh CA, Altshuler D, Chakravarti A, et al. Association between microdeletion and microduplication at 16p11.2 and autism. The New England Journal of Medicine. 358: 667-75. PMID 18184952 DOI: 10.1056/NEJMoa075974  0.6
2008 Cross S, Kim SJ, Weiss LA, Delahanty RJ, Sutcliffe JS, Leventhal BL, Cook EH, Veenstra-Vanderweele J. Molecular genetics of the platelet serotonin system in first-degree relatives of patients with autism. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 33: 353-60. PMID 17406648 DOI: 10.1038/sj.npp.1301406  0.6
2007 Thompson EE, Pan L, Ostrovnaya I, Weiss LA, Gern JE, Lemanske RF, Nicolae DL, Ober C. Integrin beta 3 genotype influences asthma and allergy phenotypes in the first 6 years of life. The Journal of Allergy and Clinical Immunology. 119: 1423-9. PMID 17556058 DOI: 10.1016/j.jaci.2007.03.029  0.6
2007 Weiss LA, Purcell S, Waggoner S, Lawrence K, Spektor D, Daly MJ, Sklar P, Skuse D. Identification of EFHC2 as a quantitative trait locus for fear recognition in Turner syndrome. Human Molecular Genetics. 16: 107-13. PMID 17164267 DOI: 10.1093/hmg/ddl445  0.6
2006 Weiss LA, Barrett-Connor E, von Mühlen D, Clark P. Leptin predicts BMD and bone resorption in older women but not older men: the Rancho Bernardo study. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 21: 758-64. PMID 16734391 DOI: 10.1359/jbmr.060206  0.6
2006 Weiss LA, Langenberg C, Barrett-Connor E. Ghrelin and bone: is there an association in older adults?: the Rancho Bernardo study. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 21: 752-7. PMID 16734390 DOI: 10.1359/jbmr.060209  0.6
2006 Weiss LA, Kosova G, Delahanty RJ, Jiang L, Cook EH, Ober C, Sutcliffe JS. Variation in ITGB3 is associated with whole-blood serotonin level and autism susceptibility. European Journal of Human Genetics : Ejhg. 14: 923-31. PMID 16724005 DOI: 10.1038/sj.ejhg.5201644  0.6
2006 Weiss LA, Ober C, Cook EH. ITGB3 shows genetic and expression interaction with SLC6A4. Human Genetics. 120: 93-100. PMID 16721604 DOI: 10.1007/s00439-006-0196-z  0.6
2006 Weiss LA, Pan L, Abney M, Ober C. The sex-specific genetic architecture of quantitative traits in humans. Nature Genetics. 38: 218-22. PMID 16429159 DOI: 10.1038/ng1726  0.6
2005 Kurina LM, Weiss LA, Graves SW, Parry R, Williams GH, Abney M, Ober C. Sex differences in the genetic basis of morning serum cortisol levels: genome-wide screen identifies two novel loci specific to women. The Journal of Clinical Endocrinology and Metabolism. 90: 4747-52. PMID 15941864 DOI: 10.1210/jc.2005-0384  0.6
2005 Weiss LA, Abney M, Parry R, Scanu AM, Cook EH, Ober C. Variation in ITGB3 has sex-specific associations with plasma lipoprotein(a) and whole blood serotonin levels in a population-based sample. Human Genetics. 117: 81-7. PMID 15834589 DOI: 10.1007/s00439-004-1250-3  0.6
2005 Weiss LA, Barrett-Connor E, von Mühlen D. Ratio of n-6 to n-3 fatty acids and bone mineral density in older adults: the Rancho Bernardo Study. The American Journal of Clinical Nutrition. 81: 934-8. PMID 15817874  0.6
2005 Weiss LA, Lester LA, Gern JE, Wolf RL, Parry R, Lemanske RF, Solway J, Ober C. Variation in ITGB3 is associated with asthma and sensitization to mold allergen in four populations. American Journal of Respiratory and Critical Care Medicine. 172: 67-73. PMID 15817799 DOI: 10.1164/rccm.200411-1555OC  0.6
2005 Weiss LA, Abney M, Cook EH, Ober C. Sex-specific genetic architecture of whole blood serotonin levels. American Journal of Human Genetics. 76: 33-41. PMID 15526234 DOI: 10.1086/426697  0.6
2004 Weiss LA, Veenstra-Vanderweele J, Newman DL, Kim SJ, Dytch H, McPeek MS, Cheng S, Ober C, Cook EH, Abney M. Genome-wide association study identifies ITGB3 as a QTL for whole blood serotonin. European Journal of Human Genetics : Ejhg. 12: 949-54. PMID 15292919 DOI: 10.1038/sj.ejhg.5201239  0.6
2003 Harris MM, Houtkooper LB, Stanford VA, Parkhill C, Weber JL, Flint-Wagner H, Weiss L, Going SB, Lohman TG. Dietary iron is associated with bone mineral density in healthy postmenopausal women. The Journal of Nutrition. 133: 3598-602. PMID 14608080  0.6
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