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Sharon Schwartz - Publications

Affiliations: 
Columbia University, New York, NY 
Area:
Epidemiology
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Year Citation  Score
2017 Schwartz S, Gatto NM, Campbell UB. Heeding the call for less casual causal inferences: the utility of realized (quantitative) causal effects. Annals of Epidemiology. 27: 402-405. PMID 28641760 DOI: 10.1016/J.Annepidem.2017.05.012  0.739
2016 Schwartz S, Gatto NM, Campbell UB. Causal identification: a charge of epidemiology in danger of marginalization. Annals of Epidemiology. PMID 27237595 DOI: 10.1016/J.Annepidem.2016.03.013  0.746
2015 Schwartz S, Prins SJ, Campbell UB, Gatto NM. Is the "well-defined intervention assumption" politically conservative? Social Science & Medicine (1982). PMID 26777446 DOI: 10.1016/J.Socscimed.2015.10.054  0.724
2015 Sohler N, Adams BG, Barnes DM, Cohen GH, Prins SJ, Schwartz S. Weighing the Evidence for Harm From Long-Term Treatment With Antipsychotic Medications: A Systematic Review. The American Journal of Orthopsychiatry. PMID 26652608 DOI: 10.1037/Ort0000106  0.575
2015 Schwartz S, Campbell UB, Gatto NM, Gordon K. Toward a clarification of the taxonomy of "bias" in epidemiology textbooks. Epidemiology (Cambridge, Mass.). 26: 216-22. PMID 25536455 DOI: 10.1097/Ede.0000000000000224  0.734
2014 Gatto NM, Campbell UB, Schwartz S. The authors respond. Epidemiology (Cambridge, Mass.). 25: 619-20. PMID 24887170 DOI: 10.1097/EDE.0000000000000125  0.716
2014 Gatto NM, Campbell UB, Schwartz S. An organizational schema for epidemiologic causal effects. Epidemiology (Cambridge, Mass.). 25: 88-97. PMID 24276524 DOI: 10.1097/Ede.0000000000000005  0.753
2012 Schwartz S, Gatto NM, Campbell UB. Extending the sufficient component cause model to describe the Stable Unit Treatment Value Assumption (SUTVA). Epidemiologic Perspectives & Innovations : Ep+I. 9: 3. PMID 22472125 DOI: 10.1186/1742-5573-9-3  0.728
2011 Schwartz S, Gatto NM, Campbell UB. Transportability and causal generalization. Epidemiology (Cambridge, Mass.). 22: 745-6. PMID 21811113 DOI: 10.1097/Ede.0B013E3182254B8F  0.709
2010 Schwartz S, Hafeman D, Campbell U, Gatto N. Author response. Commentary: gilding the black box. International Journal of Epidemiology. 39: 1399-401. PMID 21105265 DOI: 10.1093/Ije/Dyp323  0.706
2010 Gatto NM, Campbell UB, Schwartz S. Author's response to Poole, C. Commentary: How Many Are Affected? A Real Limit of Epidemiology. Epidemiologic Perspectives & Innovations : Ep+I. 7: 7. PMID 20796296 DOI: 10.1186/1742-5573-7-7  0.746
2009 Hafeman DM, Schwartz S. Opening the Black Box: a motivation for the assessment of mediation. International Journal of Epidemiology. 38: 838-45. PMID 19261660 DOI: 10.1093/Ije/Dyn372  0.614
2008 Hafeman D, Schwartz S. Assessing mediation: the necessity of theoretical considerations. Preventive Medicine. 46: 610-1. PMID 17720237 DOI: 10.1016/J.Ypmed.2007.07.023  0.567
2005 Campbell UB, Gatto NM, Schwartz S. Distributional interaction: Interpretational problems when using incidence odds ratios to assess interaction. Epidemiologic Perspectives & Innovations : Ep+I. 2: 1. PMID 15745447 DOI: 10.1186/1742-5573-2-1  0.728
1994 Schwartz S. The fallacy of the ecological fallacy: The potential misuse of a concept and the consequences American Journal of Public Health. 84: 819-824. PMID 8179055 DOI: 10.2105/Ajph.84.5.819  0.32
Low-probability matches (unlikely to be authored by this person)
2000 Terry MB, Neugut AI, Schwartz S, Susser E. Risk factors for a causal intermediate and an endpoint: Reconciling differences American Journal of Epidemiology. 151: 339-345. PMID 10695592 DOI: 10.1093/Oxfordjournals.Aje.A010212  0.283
2006 Schwartz S, Susser E. Commentary: what can epidemiology accomplish? International Journal of Epidemiology. 35: 587-90; discussion 5. PMID 16540535 DOI: 10.1093/Ije/Dyl005  0.275
2002 Schwartz S. Outcomes for the sociology of mental health: are we meeting our goals? Journal of Health and Social Behavior. 43: 223-35. PMID 12096701 DOI: 10.2307/3090198  0.275
1996 Link BG, Schwartz S, Moore R, Phelan J, Struening E, Stueve A, Colten ME. Public knowledge, attitudes, and beliefs about homeless people: evidence for compassion fatigue. American Journal of Community Psychology. 23: 533-55. PMID 8546109 DOI: 10.1007/Bf02506967  0.271
2017 Schwartz S. Commentary: on the application of potential outcomes-based methods to questions in social psychiatry and psychiatric epidemiology. Social Psychiatry and Psychiatric Epidemiology. PMID 28180929 DOI: 10.1007/S00127-016-1334-0  0.265
2010 Schwartz S, Meyer IH. Mental health disparities research: the impact of within and between group analyses on tests of social stress hypotheses. Social Science & Medicine (1982). 70: 1111-8. PMID 20100631 DOI: 10.1016/J.Socscimed.2009.11.032  0.265
1990 Dohrenwend BP, Schwartz S. Socioeconomic status and psychiatric disorders Current Opinion in Psychiatry. 8: 138-141. DOI: 10.1097/00001504-199010000-00030  0.262
1999 Schwartz S, Carpenter KM. The right answer for the wrong question: Consequences of type III error for public health research American Journal of Public Health. 89: 1175-1180. PMID 10432902 DOI: 10.2105/Ajph.89.8.1175  0.26
2013 Schwartz S, Susser E. The use of well controls: an unhealthy practice in psychiatric research. Psychological Medicine. 41: 1127-31. PMID 20810003 DOI: 10.1017/S0033291710001595  0.26
1992 Dohrenwend BP, Levav I, Shrout PE, Schwartz S, Naveh G, Link BG, Skodol AE, Stueve A. Socioeconomic status and psychiatric disorders: The causation-selection issue Science. 255: 946-951. PMID 1546291 DOI: 10.1126/Science.1546291  0.257
1989 Link BG, Schwartz s. The ‘well control’ artefact in case/control studies of specific psychiatric disorders Psychological Medicine. 19: 737-742. PMID 2798641 DOI: 10.1017/S0033291700024338  0.256
2000 Schwartz S, Weiss L, Lennon MC. Labeling effects of a controversial psychiatric diagnosis: a vignette experiment of late luteal phase dysphoric disorder. Women & Health. 30: 63-75. PMID 10943803 DOI: 10.1300/J013V30N03_05  0.251
1991 Schwartz S, Link BG, Dohrenwend BP, Naveh G, Levav I, Shrout P. Separating Class and Ethnic Prejudice: A Study of North African and European Jews in Israel Social Psychology Quarterly. 54: 287. DOI: 10.2307/2786842  0.251
1993 Levav I, Kohn R, Dohrenwend BP, Shrout PE, Skodol AE, Schwartz S, Link BG, Naveh G. An epidemiological study of mental disorders in a 10-year cohort of young adults in israel Psychological Medicine. 23: 691-707. PMID 8234576 DOI: 10.1017/S0033291700025472  0.249
2001 Schwartz S, Diez-Roux AV, Diez-Roux R. Commentary: causes of incidence and causes of cases--a Durkheimian perspective on Rose. International Journal of Epidemiology. 30: 435-9. PMID 11416059 DOI: 10.1093/Ije/30.3.435  0.246
2008 Meyer IH, Dietrich J, Schwartz S. Lifetime prevalence of mental disorders and suicide attempts in diverse lesbian, gay, and bisexual populations. American Journal of Public Health. 98: 1004-6. PMID 17901444 DOI: 10.2105/Ajph.2006.096826  0.244
2011 O'Donnell S, Meyer IH, Schwartz S. Increased risk of suicide attempts among Black and Latino lesbians, gay men, and bisexuals. American Journal of Public Health. 101: 1055-9. PMID 21493928 DOI: 10.2105/Ajph.2010.300032  0.241
1994 Schwartz S, Dohrenwend BP, Levav I. Nongenetic Familial Transmission of Psychiatric Disorders? Evidence from Children of Holocaust Survivors Journal of Health and Social Behavior. 35: 385. DOI: 10.2307/2137216  0.24
1989 Markowitz JS, Gutterman EM, Schwartz S, Link B, Gorman SM. Acute health effects among firefighters exposed to a Polyvinyl Chloride (PVC) fire American Journal of Epidemiology. 129: 1023-1031. PMID 2705423 DOI: 10.1093/Oxfordjournals.Aje.A115206  0.239
1991 Schwartz S. Women and depression: A Durkheimian perspective Social Science and Medicine. 32: 127-140. PMID 2014408 DOI: 10.1016/0277-9536(91)90052-E  0.235
1996 Skodol AE, Schwartz S, Dohrenwend BP, Levav I, Shrout PE, Reiff M. PTSD symptoms and comorbid mental disorders in Israeli war veterans British Journal of Psychiatry. 169: 717-725. PMID 8968629 DOI: 10.1192/Bjp.169.6.717  0.235
2015 Meyer IH, Teylan M, Schwartz S. The role of help-seeking in preventing suicide attempts among lesbians, gay men, and bisexuals. Suicide & Life-Threatening Behavior. 45: 25-36. PMID 24825437 DOI: 10.1111/Sltb.12104  0.234
2010 Schwartz S, Meyer IH. Reflections on the stress model: A response to Turner Social Science & Medicine. 70: 1121-1122. DOI: 10.1016/J.Socscimed.2009.11.038  0.229
1992 Marbach JJ, Schwartz S, Link BG. The control group conundrum in chronic pain case/control studies Clinical Journal of Pain. 8: 39-43. PMID 1576418 DOI: 10.1097/00002508-199203000-00008  0.228
2008 Meyer IH, Schwartz S, Frost DM. Social patterning of stress and coping: does disadvantaged social statuses confer more stress and fewer coping resources? Social Science & Medicine (1982). 67: 368-79. PMID 18433961 DOI: 10.1016/J.Socscimed.2008.03.012  0.228
2016 Frost DM, Meyer IH, Schwartz S. Social support networks among diverse sexual minority populations. The American Journal of Orthopsychiatry. 86: 91-102. PMID 26752447 DOI: 10.1037/Ort0000117  0.226
2007 Schwartz S. Distinguishing distress from disorder as psychological outcomes of stressful social arrangements: can we and should we? Health (London, England : 1997). 11: 291-9; discussion 32. PMID 17606694 DOI: 10.1177/1363459307077542  0.221
2001 Reiff M, Schwartz S, Northridge M. Relationship of depressive symptoms to hypertension in a Household Survey in Harlem Psychosomatic Medicine. 63: 711-721. PMID 11573017 DOI: 10.1097/00006842-200109000-00002  0.221
1994 Skodol AE, Schwartz S, Dohrenwend BP, Levav I, Shrout PE. Minor Depression in a Cohort of Young Adults in Israel Archives of General Psychiatry. 51: 542-551. PMID 8031227 DOI: 10.1001/Archpsyc.1994.03950070034008  0.215
2000 Meyer IH, Schwartz S. Social issues as public health: promise and peril. American Journal of Public Health. 90: 1189. PMID 10936991 DOI: 10.2105/Ajph.90.8.1189  0.209
2010 Schwartz S, Susser E. Genome-wide association studies: does only size matter? The American Journal of Psychiatry. 167: 741-4. PMID 20595425 DOI: 10.1176/Appi.Ajp.2010.10030465  0.201
1999 Schwartz S, Susser E, Susser M. A future for epidemiology? Annual Review of Public Health. 20: 15-33. PMID 10352847 DOI: 10.1146/annurev.publhealth.20.1.15  0.189
2003 Rundle A, Schwartz S. Issues in the epidemiological analysis and interpretation of intermediate biomarkers. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 12: 491-6. PMID 12814992  0.144
2018 Reese JB, Sorice KA, Oppenheimer NM, Smith KC, Bober SL, Bantug ET, Schwartz SC, Porter LS. Why do breast cancer survivors decline a couple-based intimacy enhancement intervention trial? Translational Behavioral Medicine. PMID 30544201 DOI: 10.1093/tbm/iby129  0.143
2018 Reese JB, Smith KC, Handorf E, Sorice K, Bober SL, Bantug ET, Schwartz S, Porter LS. A randomized pilot trial of a couple-based intervention addressing sexual concerns for breast cancer survivors. Journal of Psychosocial Oncology. 1-22. PMID 30580675 DOI: 10.1080/07347332.2018.1510869  0.124
2016 Reese JB, Porter LS, Casale KE, Bantug ET, Bober SL, Schwartz SC, Smith KC. Adapting a couple-based intimacy enhancement intervention to breast cancer: A developmental study. Health Psychology : Official Journal of the Division of Health Psychology, American Psychological Association. 35: 1085-96. PMID 27657981 DOI: 10.1037/hea0000413  0.11
2019 Forman A, Schwartz S. Guidelines-Based Cancer Risk Assessment. Seminars in Oncology Nursing. PMID 30683549 DOI: 10.1016/j.soncn.2018.12.010  0.091
2005 Roman AJ, Schwartz SB, Aleman TS, Cideciyan AV, Chico JD, Windsor EA, Gardner LM, Ying GS, Smilko EE, Maguire MG, Jacobson SG. Quantifying rod photoreceptor-mediated vision in retinal degenerations: dark-adapted thresholds as outcome measures. Experimental Eye Research. 80: 259-72. PMID 15670804 DOI: 10.1016/J.Exer.2004.09.008  0.085
2004 Cideciyan AV, Aleman TS, Swider M, Schwartz SB, Steinberg JD, Brucker AJ, Maguire AM, Bennett J, Stone EM, Jacobson SG. Mutations in ABCA4 result in accumulation of lipofuscin before slowing of the retinoid cycle: a reappraisal of the human disease sequence. Human Molecular Genetics. 13: 525-34. PMID 14709597 DOI: 10.1093/Hmg/Ddh048  0.084
2010 Banin E, Bandah-Rozenfeld D, Obolensky A, Cideciyan AV, Aleman TS, Marks-Ohana D, Sela M, Boye S, Sumaroka A, Roman AJ, Schwartz SB, Hauswirth WW, Jacobson SG, Hemo I, Sharon D. Molecular anthropology meets genetic medicine to treat blindness in the North African Jewish population: human gene therapy initiated in Israel. Human Gene Therapy. 21: 1749-57. PMID 20604683 DOI: 10.1089/Hum.2010.047  0.083
2015 Luo X, Cideciyan AV, Iannaccone A, Roman AJ, Ditta LC, Jennings BJ, Yatsenko SA, Sheplock R, Sumaroka A, Swider M, Schwartz SB, Wissinger B, Kohl S, Jacobson SG. Blue cone monochromacy: visual function and efficacy outcome measures for clinical trials. Plos One. 10: e0125700. PMID 25909963 DOI: 10.1371/journal.pone.0125700  0.08
2011 Jacobson SG, Cideciyan AV, Gibbs D, Sumaroka A, Roman AJ, Aleman TS, Schwartz SB, Olivares MB, Russell RC, Steinberg JD, Kenna MA, Kimberling WJ, Rehm HL, Williams DS. Retinal disease course in Usher syndrome 1B due to MYO7A mutations. Investigative Ophthalmology & Visual Science. 52: 7924-36. PMID 21873662 DOI: 10.1167/Iovs.11-8313  0.078
2007 Jacobson SG, Cideciyan AV, Aleman TS, Sumaroka A, Schwartz SB, Roman AJ, Stone EM. Leber congenital amaurosis caused by an RPGRIP1 mutation shows treatment potential. Ophthalmology. 114: 895-8. PMID 17306875 DOI: 10.1016/J.Ophtha.2006.10.028  0.078
2012 Cideciyan AV, Swider M, Aleman TS, Feuer WJ, Schwartz SB, Russell RC, Steinberg JD, Stone EM, Jacobson SG. Macular function in macular degenerations: repeatability of microperimetry as a potential outcome measure for ABCA4-associated retinopathy trials. Investigative Ophthalmology & Visual Science. 53: 841-52. PMID 22247458 DOI: 10.1167/Iovs.11-8415  0.077
2011 Stone EM, Cideciyan AV, Aleman TS, Scheetz TE, Sumaroka A, Ehlinger MA, Schwartz SB, Fishman GA, Traboulsi EI, Lam BL, Fulton AB, Mullins RF, Sheffield VC, Jacobson SG. Variations in NPHP5 in patients with nonsyndromic leber congenital amaurosis and Senior-Loken syndrome. Archives of Ophthalmology (Chicago, Ill. : 1960). 129: 81-7. PMID 21220633 DOI: 10.1001/Archophthalmol.2010.330  0.076
2015 Roman AJ, Cideciyan AV, Matsui R, Sheplock R, Schwartz SB, Jacobson SG. Outcome measure for the treatment of cone photoreceptor diseases: orientation to a scene with cone-only contrast. Bmc Ophthalmology. 15: 98. PMID 26253563 DOI: 10.1186/s12886-015-0085-0  0.076
2009 Cideciyan AV, Swider M, Aleman TS, Tsybovsky Y, Schwartz SB, Windsor EA, Roman AJ, Sumaroka A, Steinberg JD, Jacobson SG, Stone EM, Palczewski K. ABCA4 disease progression and a proposed strategy for gene therapy. Human Molecular Genetics. 18: 931-41. PMID 19074458 DOI: 10.1093/Hmg/Ddn421  0.075
2008 Cideciyan AV, Aleman TS, Boye SL, Schwartz SB, Kaushal S, Roman AJ, Pang JJ, Sumaroka A, Windsor EA, Wilson JM, Flotte TR, Fishman GA, Heon E, Stone EM, Byrne BJ, et al. Human gene therapy for RPE65 isomerase deficiency activates the retinoid cycle of vision but with slow rod kinetics. Proceedings of the National Academy of Sciences of the United States of America. 105: 15112-7. PMID 18809924 DOI: 10.1073/Pnas.0807027105  0.074
2006 Jacobson SG, Cideciyan AV, Sumaroka A, Aleman TS, Schwartz SB, Windsor EA, Roman AJ, Stone EM, MacDonald IM. Remodeling of the human retina in choroideremia: rab escort protein 1 (REP-1) mutations. Investigative Ophthalmology & Visual Science. 47: 4113-20. PMID 16936131 DOI: 10.1167/Iovs.06-0424  0.073
2012 Jacobson SG, Cideciyan AV, Ratnakaram R, Heon E, Schwartz SB, Roman AJ, Peden MC, Aleman TS, Boye SL, Sumaroka A, Conlon TJ, Calcedo R, Pang JJ, Erger KE, Olivares MB, et al. Gene therapy for leber congenital amaurosis caused by RPE65 mutations: safety and efficacy in 15 children and adults followed up to 3 years. Archives of Ophthalmology (Chicago, Ill. : 1960). 130: 9-24. PMID 21911650 DOI: 10.1001/Archophthalmol.2011.298  0.072
2011 Cideciyan AV, Rachel RA, Aleman TS, Swider M, Schwartz SB, Sumaroka A, Roman AJ, Stone EM, Jacobson SG, Swaroop A. Cone photoreceptors are the main targets for gene therapy of NPHP5 (IQCB1) or NPHP6 (CEP290) blindness: generation of an all-cone Nphp6 hypomorph mouse that mimics the human retinal ciliopathy. Human Molecular Genetics. 20: 1411-23. PMID 21245082 DOI: 10.1093/Hmg/Ddr022  0.071
2013 Zeitz C, Jacobson SG, Hamel CP, Bujakowska K, Neuillé M, Orhan E, Zanlonghi X, Lancelot ME, Michiels C, Schwartz SB, Bocquet B, Antonio A, Audier C, Letexier M, et al. Whole-exome sequencing identifies LRIT3 mutations as a cause of autosomal-recessive complete congenital stationary night blindness. American Journal of Human Genetics. 92: 67-75. PMID 23246293 DOI: 10.1016/J.Ajhg.2012.10.023  0.069
2008 Hauswirth WW, Aleman TS, Kaushal S, Cideciyan AV, Schwartz SB, Wang L, Conlon TJ, Boye SL, Flotte TR, Byrne BJ, Jacobson SG. Treatment of leber congenital amaurosis due to RPE65 mutations by ocular subretinal injection of adeno-associated virus gene vector: short-term results of a phase I trial. Human Gene Therapy. 19: 979-90. PMID 18774912 DOI: 10.1089/Hum.2008.107  0.069
2011 Stone EM, Luo X, Héon E, Lam BL, Weleber RG, Halder JA, Affatigato LM, Goldberg JB, Sumaroka A, Schwartz SB, Cideciyan AV, Jacobson SG. Autosomal recessive retinitis pigmentosa caused by mutations in the MAK gene. Investigative Ophthalmology & Visual Science. 52: 9665-73. PMID 22110072 DOI: 10.1167/Iovs.11-8527  0.067
2009 Cideciyan AV, Hauswirth WW, Aleman TS, Kaushal S, Schwartz SB, Boye SL, Windsor EA, Conlon TJ, Sumaroka A, Roman AJ, Byrne BJ, Jacobson SG. Vision 1 year after gene therapy for Leber's congenital amaurosis. The New England Journal of Medicine. 361: 725-7. PMID 19675341 DOI: 10.1056/Nejmc0903652  0.065
2007 Cideciyan AV, Swider M, Aleman TS, Roman MI, Sumaroka A, Schwartz SB, Stone EM, Jacobson SG. Reduced-illuminance autofluorescence imaging in ABCA4-associated retinal degenerations. Journal of the Optical Society of America. a, Optics, Image Science, and Vision. 24: 1457-67. PMID 17429493 DOI: 10.1364/Josaa.24.001457  0.064
2005 Susser E, Schwartz S. Are social causes so different from all other causes? A comment on Sander Greenland. Emerging Themes in Epidemiology. 2: 4. PMID 15913455 DOI: 10.1186/1742-7622-2-4  0.064
2006 Jacobson SG, Boye SL, Aleman TS, Conlon TJ, Zeiss CJ, Roman AJ, Cideciyan AV, Schwartz SB, Komaromy AM, Doobrajh M, Cheung AY, Sumaroka A, Pearce-Kelling SE, Aguirre GD, Kaushal S, et al. Safety in nonhuman primates of ocular AAV2-RPE65, a candidate treatment for blindness in Leber congenital amaurosis. Human Gene Therapy. 17: 845-58. PMID 16942444 DOI: 10.1089/Hum.2006.17.845  0.062
2005 Schwartz SB, Aleman TS, Cideciyan AV, Windsor EA, Sumaroka A, Roman AJ, Rane T, Smilko EE, Bennett J, Stone EM, Kimberling WJ, Liu XZ, Jacobson SG. Disease expression in Usher syndrome caused by VLGR1 gene mutation (USH2C) and comparison with USH2A phenotype. Investigative Ophthalmology & Visual Science. 46: 734-43. PMID 15671307 DOI: 10.1167/Iovs.04-1136  0.061
2013 Jacobson SG, Cideciyan AV, Peshenko IV, Sumaroka A, Olshevskaya EV, Cao L, Schwartz SB, Roman AJ, Olivares MB, Sadigh S, Yau KW, Heon E, Stone EM, Dizhoor AM. Determining consequences of retinal membrane guanylyl cyclase (RetGC1) deficiency in human Leber congenital amaurosis en route to therapy: residual cone-photoreceptor vision correlates with biochemical properties of the mutants. Human Molecular Genetics. 22: 168-83. PMID 23035049 DOI: 10.1093/Hmg/Dds421  0.06
2006 Jacobson SG, Acland GM, Aguirre GD, Aleman TS, Schwartz SB, Cideciyan AV, Zeiss CJ, Komaromy AM, Kaushal S, Roman AJ, Windsor EA, Sumaroka A, Pearce-Kelling SE, Conlon TJ, Chiodo VA, et al. Safety of recombinant adeno-associated virus type 2-RPE65 vector delivered by ocular subretinal injection. Molecular Therapy : the Journal of the American Society of Gene Therapy. 13: 1074-84. PMID 16644289 DOI: 10.1016/J.Ymthe.2006.03.005  0.06
2012 Huang WC, Wright AF, Roman AJ, Cideciyan AV, Manson FD, Gewaily DY, Schwartz SB, Sadigh S, Limberis MP, Bell P, Wilson JM, Swaroop A, Jacobson SG. RPGR-associated retinal degeneration in human X-linked RP and a murine model. Investigative Ophthalmology & Visual Science. 53: 5594-608. PMID 22807293 DOI: 10.1167/Iovs.12-10070  0.06
2005 Cideciyan AV, Swider M, Aleman TS, Sumaroka A, Schwartz SB, Roman MI, Milam AH, Bennett J, Stone EM, Jacobson SG. ABCA4-associated retinal degenerations spare structure and function of the human parapapillary retina. Investigative Ophthalmology & Visual Science. 46: 4739-46. PMID 16303974 DOI: 10.1167/Iovs.05-0805  0.06
2008 Jacobson SG, Cideciyan AV, Aleman TS, Sumaroka A, Roman AJ, Gardner LM, Prosser HM, Mishra M, Bech-Hansen NT, Herrera W, Schwartz SB, Liu XZ, Kimberling WJ, Steel KP, Williams DS. Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism. Human Molecular Genetics. 17: 2405-15. PMID 18463160 DOI: 10.1093/Hmg/Ddn140  0.06
2011 Aleman TS, Cideciyan AV, Aguirre GK, Huang WC, Mullins CL, Roman AJ, Sumaroka A, Olivares MB, Tsai FF, Schwartz SB, Vandenberghe LH, Limberis MP, Stone EM, Bell P, Wilson JM, et al. Human CRB1-associated retinal degeneration: comparison with the rd8 Crb1-mutant mouse model. Investigative Ophthalmology & Visual Science. 52: 6898-910. PMID 21757580 DOI: 10.1167/Iovs.11-7701  0.059
2013 Cideciyan AV, Jacobson SG, Beltran WA, Sumaroka A, Swider M, Iwabe S, Roman AJ, Olivares MB, Schwartz SB, Komáromy AM, Hauswirth WW, Aguirre GD. Human retinal gene therapy for Leber congenital amaurosis shows advancing retinal degeneration despite enduring visual improvement. Proceedings of the National Academy of Sciences of the United States of America. 110: E517-25. PMID 23341635 DOI: 10.1073/Pnas.1218933110  0.058
2009 Cideciyan AV, Hauswirth WW, Aleman TS, Kaushal S, Schwartz SB, Boye SL, Windsor EA, Conlon TJ, Sumaroka A, Pang JJ, Roman AJ, Byrne BJ, Jacobson SG. Human RPE65 gene therapy for Leber congenital amaurosis: persistence of early visual improvements and safety at 1 year. Human Gene Therapy. 20: 999-1004. PMID 19583479 DOI: 10.1089/Hum.2009.086  0.057
2005 Jacobson SG, Aleman TS, Cideciyan AV, Sumaroka A, Schwartz SB, Windsor EA, Traboulsi EI, Heon E, Pittler SJ, Milam AH, Maguire AM, Palczewski K, Stone EM, Bennett J. Identifying photoreceptors in blind eyes caused by RPE65 mutations: Prerequisite for human gene therapy success. Proceedings of the National Academy of Sciences of the United States of America. 102: 6177-82. PMID 15837919 DOI: 10.1073/Pnas.0500646102  0.056
2016 Charng J, Cideciyan AV, Jacobson SG, Sumaroka A, Schwartz SB, Swider M, Roman AJ, Sheplock R, Anand M, Peden MC, Khanna H, Heon E, Wright AF, Swaroop A. Variegated yet Non-Random Rod and Cone Photoreceptor Disease Patterns in RPGR-ORF15-associated Retinal Degeneration. Human Molecular Genetics. PMID 27798110 DOI: 10.1093/Hmg/Ddw361  0.056
2006 Azari AA, Aleman TS, Cideciyan AV, Schwartz SB, Windsor EA, Sumaroka A, Cheung AY, Steinberg JD, Roman AJ, Stone EM, Sheffield VC, Jacobson SG. Retinal disease expression in Bardet-Biedl syndrome-1 (BBS1) is a spectrum from maculopathy to retina-wide degeneration. Investigative Ophthalmology & Visual Science. 47: 5004-10. PMID 17065520 DOI: 10.1167/Iovs.06-0517  0.055
1998 Schwartz S, Lincoln A, Levav I. In menstrual cycle stage a confounder in population-based psychiatric research? Psychological Medicine. 27: 1435-9. PMID 9403914 DOI: 10.1017/S003329179700514X  0.055
2011 Jacobson SG, Cideciyan AV, Aleman TS, Sumaroka A, Roman AJ, Swider M, Schwartz SB, Banin E, Stone EM. Human retinal disease from AIPL1 gene mutations: foveal cone loss with minimal macular photoreceptors and rod function remaining. Investigative Ophthalmology & Visual Science. 52: 70-9. PMID 20702822 DOI: 10.1167/Iovs.10-6127  0.054
2017 Jacobson SG, Cideciyan AV, Sumaroka A, Roman AJ, Charng J, Lu M, Choudhury S, Schwartz SB, Heon E, Fishman GA, Boye SE. Defining Outcomes for Clinical Trials of Leber Congenital Amaurosis caused by GUCY2D Mutations. American Journal of Ophthalmology. PMID 28212877 DOI: 10.1016/J.Ajo.2017.02.003  0.054
2012 Dinculescu A, Estreicher J, Zenteno JC, Aleman TS, Schwartz SB, Huang WC, Roman AJ, Sumaroka A, Li Q, Deng WT, Min SH, Chiodo VA, Neeley A, Liu X, Shu X, et al. Gene therapy for retinitis pigmentosa caused by MFRP mutations: human phenotype and preliminary proof of concept. Human Gene Therapy. 23: 367-76. PMID 22142163 DOI: 10.1089/Hum.2011.169  0.054
2004 Wright AF, Reddick AC, Schwartz SB, Ferguson JS, Aleman TS, Kellner U, Jurklies B, Schuster A, Zrenner E, Wissinger B, Lennon A, Shu X, Cideciyan AV, Stone EM, Jacobson SG, et al. Mutation analysis of NR2E3 and NRL genes in Enhanced S Cone Syndrome. Human Mutation. 24: 439. PMID 15459973 DOI: 10.1002/Humu.9285  0.053
2004 Jacobson SG, Sumaroka A, Aleman TS, Cideciyan AV, Schwartz SB, Roman AJ, McInnes RR, Sheffield VC, Stone EM, Swaroop A, Wright AF. Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degeneration. Human Molecular Genetics. 13: 1893-902. PMID 15229190 DOI: 10.1093/Hmg/Ddh198  0.052
2016 Matsui R, McGuigan Iii DB, Gruzensky ML, Aleman TS, Schwartz SB, Sumaroka A, Koenekoop RK, Cideciyan AV, Jacobson SG. SPATA7: Evolving phenotype from cone-rod dystrophy to retinitis pigmentosa. Ophthalmic Genetics. 1-6. PMID 26854980 DOI: 10.3109/13816810.2015.1130154  0.052
2013 Cideciyan AV, Hufnagel RB, Carroll J, Sumaroka A, Luo X, Schwartz SB, Dubra A, Land M, Michaelides M, Gardner JC, Hardcastle AJ, Moore AT, Sisk RA, Ahmed ZM, Kohl S, et al. Human cone visual pigment deletions spare sufficient photoreceptors to warrant gene therapy. Human Gene Therapy. 24: 993-1006. PMID 24067079 DOI: 10.1089/Hum.2013.153  0.051
2003 Jacobson SG, Cideciyan AV, Aleman TS, Pianta MJ, Sumaroka A, Schwartz SB, Smilko EE, Milam AH, Sheffield VC, Stone EM. Crumbs homolog 1 (CRB1) mutations result in a thick human retina with abnormal lamination. Human Molecular Genetics. 12: 1073-8. PMID 12700176 DOI: 10.1093/Hmg/Ddg117  0.051
2017 Jacobson SG, Cideciyan AV, Sumaroka A, Roman AJ, Charng J, Lu M, Choi W, Sheplock R, Swider M, Kosyk MS, Schwartz SB, Stone EM, Fishman GA. Outcome Measures for Clinical Trials of Leber Congenital Amaurosis Caused by the Intronic Mutation in the CEP290 Gene. Investigative Ophthalmology & Visual Science. 58: 2609-2622. PMID 28510626 DOI: 10.1167/Iovs.17-21560  0.051
2018 Charng J, Cideciyan AV, Jacobson SG, Sumaroka A, Schwartz SB, Swider M, Roman AJ, Sheplock R, Anand M, Peden MC, Khanna H, Heon E, Wright AF, Swaroop A. Variegated yet non-random rod and cone photoreceptor disease patterns in RPGR-ORF15-associated retinal degeneration. Human Molecular Genetics. PMID 30285110 DOI: 10.1093/hmg/ddy342  0.051
2016 Jacobson SG, Cideciyan AV, Huang WC, Sumaroka A, Nam HJ, Sheplock R, Schwartz SB. Leber Congenital Amaurosis: Genotypes and Retinal Structure Phenotypes. Advances in Experimental Medicine and Biology. 854: 169-75. PMID 26427408 DOI: 10.1007/978-3-319-17121-0_23  0.051
2017 Heneghan C, Smilow E, Tanhehco Y, Jin Z, Cofnas P, Schwartz S, Patel N, Carberry D, Silverman J, Huynh P, Hagan B, Tobin K, Bhatia M, George D, Garvin J, et al. Safety of hematopoietic cell infusion in children with malignant and non-malignant diseases. Pediatric Transplantation. PMID 28845921 DOI: 10.1111/Petr.13038  0.05
1983 Sinyor D, Schwartz SG, Peronnet F, Brisson G, Seraganian P. Aerobic fitness level and reactivity to psychosocial stress: physiological, biochemical, and subjective measures. Psychosomatic Medicine. 45: 205-17. PMID 6611800 DOI: 10.1097/00006842-198306000-00003  0.05
2007 Jacobson SG, Aleman TS, Cideciyan AV, Heon E, Golczak M, Beltran WA, Sumaroka A, Schwartz SB, Roman AJ, Windsor EA, Wilson JM, Aguirre GD, Stone EM, Palczewski K. Human cone photoreceptor dependence on RPE65 isomerase. Proceedings of the National Academy of Sciences of the United States of America. 104: 15123-8. PMID 17848510 DOI: 10.1073/Pnas.0706367104  0.05
2015 Zhang N, Tsybovsky Y, Kolesnikov AV, Rozanowska M, Swider M, Schwartz SB, Stone EM, Palczewska G, Maeda A, Kefalov VJ, Jacobson SG, Cideciyan AV, Palczewski K. Protein misfolding and the pathogenesis of ABCA4-associated retinal degenerations. Human Molecular Genetics. 24: 3220-37. PMID 25712131 DOI: 10.1093/Hmg/Ddv073  0.05
2007 Jacobson SG, Cideciyan AV, Aleman TS, Sumaroka A, Schwartz SB, Windsor EA, Roman AJ, Heon E, Stone EM, Thompson DA. RDH12 and RPE65, visual cycle genes causing leber congenital amaurosis, differ in disease expression. Investigative Ophthalmology & Visual Science. 48: 332-8. PMID 17197551 DOI: 10.1167/Iovs.06-0599  0.05
2015 Zelinger L, Cideciyan AV, Kohl S, Schwartz SB, Rosenmann A, Eli D, Sumaroka A, Roman AJ, Luo X, Brown C, Rosin B, Blumenfeld A, Wissinger B, Jacobson SG, Banin E, et al. Genetics and Disease Expression in the CNGA3 Form of Achromatopsia: Steps on the Path to Gene Therapy. Ophthalmology. 122: 997-1007. PMID 25616768 DOI: 10.1016/j.ophtha.2014.11.025  0.048
2013 Roman AJ, Cideciyan AV, Schwartz SB, Olivares MB, Heon E, Jacobson SG. Intervisit variability of visual parameters in Leber congenital amaurosis caused by RPE65 mutations. Investigative Ophthalmology & Visual Science. 54: 1378-83. PMID 23341016 DOI: 10.1167/Iovs.12-11341  0.046
2016 Jacobson SG, McGuigan DB, Sumaroka A, Roman AJ, Gruzensky ML, Sheplock R, Palma J, Schwartz SB, Aleman TS, Cideciyan AV. Complexity of the Class B Phenotype in Autosomal Dominant Retinitis Pigmentosa Due to Rhodopsin Mutations. Investigative Ophthalmology & Visual Science. 57: 4847-4858. PMID 27654411 DOI: 10.1167/iovs.16-19890  0.046
2008 Jacobson SG, Cideciyan AV, Aleman TS, Sumaroka A, Windsor EA, Schwartz SB, Heon E, Stone EM. Photoreceptor layer topography in children with leber congenital amaurosis caused by RPE65 mutations. Investigative Ophthalmology & Visual Science. 49: 4573-7. PMID 18539930 DOI: 10.1167/Iovs.08-2121  0.045
2008 Herrera W, Aleman TS, Cideciyan AV, Roman AJ, Banin E, Ben-Yosef T, Gardner LM, Sumaroka A, Windsor EA, Schwartz SB, Stone EM, Liu XZ, Kimberling WJ, Jacobson SG. Retinal disease in Usher syndrome III caused by mutations in the clarin-1 gene. Investigative Ophthalmology & Visual Science. 49: 2651-60. PMID 18281613 DOI: 10.1167/Iovs.07-1505  0.045
2009 Jacobson SG, Aleman TS, Cideciyan AV, Sumaroka A, Schwartz SB, Windsor EA, Swider M, Herrera W, Stone EM. Leber congenital amaurosis caused by Lebercilin (LCA5) mutation: retained photoreceptors adjacent to retinal disorganization. Molecular Vision. 15: 1098-106. PMID 19503738  0.045
2014 Jacobson SG, Cideciyan AV, Huang WC, Sumaroka A, Roman AJ, Schwartz SB, Luo X, Sheplock R, Dauber JM, Swider M, Stone EM. TULP1 mutations causing early-onset retinal degeneration: preserved but insensitive macular cones. Investigative Ophthalmology & Visual Science. 55: 5354-64. PMID 25074776 DOI: 10.1167/Iovs.14-14570  0.044
2017 Aguirre GK, Butt OH, Datta R, Roman AJ, Sumaroka A, Schwartz SB, Cideciyan AV, Jacobson SG. Postretinal Structure and Function in Severe Congenital Photoreceptor Blindness Caused by Mutations in the GUCY2D Gene. Investigative Ophthalmology & Visual Science. 58: 959-973. PMID 28403437 DOI: 10.1167/Iovs.16-20413  0.044
2007 Aleman TS, Cideciyan AV, Sumaroka A, Schwartz SB, Roman AJ, Windsor EA, Steinberg JD, Branham K, Othman M, Swaroop A, Jacobson SG. Inner retinal abnormalities in X-linked retinitis pigmentosa with RPGR mutations. Investigative Ophthalmology & Visual Science. 48: 4759-65. PMID 17898302 DOI: 10.1167/Iovs.07-0453  0.044
2009 Aleman TS, Soumittra N, Cideciyan AV, Sumaroka AM, Ramprasad VL, Herrera W, Windsor EA, Schwartz SB, Russell RC, Roman AJ, Inglehearn CF, Kumaramanickavel G, Stone EM, Fishman GA, Jacobson SG. CERKL mutations cause an autosomal recessive cone-rod dystrophy with inner retinopathy. Investigative Ophthalmology & Visual Science. 50: 5944-54. PMID 19578027 DOI: 10.1167/Iovs.09-3982  0.043
2009 Jacobson SG, Aleman TS, Sumaroka A, Cideciyan AV, Roman AJ, Windsor EA, Schwartz SB, Rehm HL, Kimberling WJ. Disease boundaries in the retina of patients with Usher syndrome caused by MYO7A gene mutations. Investigative Ophthalmology & Visual Science. 50: 1886-94. PMID 19074810 DOI: 10.1167/iovs.08-3122  0.042
2016 Chang AK, Foca MD, Jin Z, Vasudev R, Laird M, Schwartz S, Qureshi M, Kolb M, Levinson A, Bhatia M, Kung A, Garvin J, George D, Della-Latta P, Whittier S, et al. Bacterial bloodstream infections in pediatric allogeneic hematopoietic stem cell recipients before and after implementation of a central line-associated bloodstream infection protocol: A single-center experience. American Journal of Infection Control. PMID 27378008 DOI: 10.1016/j.ajic.2016.04.229  0.042
2007 Cideciyan AV, Aleman TS, Jacobson SG, Khanna H, Sumaroka A, Aguirre GK, Schwartz SB, Windsor EA, He S, Chang B, Stone EM, Swaroop A. Centrosomal-ciliary gene CEP290/NPHP6 mutations result in blindness with unexpected sparing of photoreceptors and visual brain: implications for therapy of Leber congenital amaurosis. Human Mutation. 28: 1074-83. PMID 17554762 DOI: 10.1002/Humu.20565  0.041
2012 Branham K, Othman M, Brumm M, Karoukis AJ, Atmaca-Sonmez P, Yashar BM, Schwartz SB, Stover NB, Trzupek K, Wheaton D, Jennings B, Ciccarelli ML, Jayasundera KT, Lewis RA, Birch D, et al. Mutations in RPGR and RP2 account for 15% of males with simplex retinal degenerative disease. Investigative Ophthalmology & Visual Science. 53: 8232-7. PMID 23150612 DOI: 10.1167/Iovs.12-11025  0.041
2017 Ramamurthy C, Hitrik MA, DeMora L, Forman A, Rainey K, Savage M, Montgomery S, Masny A, Schwartz S, Hall MJ, Daly MB, Obeid E. Are we still adjusting to multigene panel testing? An NCI-designated cancer center's 2-year experience. Journal of Clinical Oncology. 35: 1585-1585. DOI: 10.1200/JCO.2017.35.15_suppl.1585  0.041
2015 Cideciyan AV, Swider M, Schwartz SB, Stone EM, Jacobson SG. Predicting Progression of ABCA4-Associated Retinal Degenerations Based on Longitudinal Measurements of the Leading Disease Front. Investigative Ophthalmology & Visual Science. 56: 5946-55. PMID 26377081 DOI: 10.1167/Iovs.15-17698  0.041
2016 Sumaroka A, Matsui R, Cideciyan AV, McGuigan DB, Sheplock R, Schwartz SB, Jacobson SG. Outer Retinal Changes Including the Ellipsoid Zone Band in Usher Syndrome 1B due to MYO7A Mutations. Investigative Ophthalmology & Visual Science. 57: OCT253-61. PMID 27409480 DOI: 10.1167/iovs.15-18860  0.039
2016 Smilow E, Heneghan C, Jin Z, Silverman P, Schwartz S, Carberry D, Tobin K, Silverman J, Hagan B, Bhatia M, George D, Garvin J, Kung A, Satwani P. A Single Center Study of Hematopoietic Cell Infusion Related Adverse Events in Children Biology of Blood and Marrow Transplantation. 22: S448-S449. DOI: 10.1016/J.Bbmt.2015.11.1024  0.037
2009 Jacobson SG, Aleman TS, Cideciyan AV, Roman AJ, Sumaroka A, Windsor EA, Schwartz SB, Heon E, Stone EM. Defining the residual vision in leber congenital amaurosis caused by RPE65 mutations. Investigative Ophthalmology & Visual Science. 50: 2368-75. PMID 19117922 DOI: 10.1167/Iovs.08-2696  0.036
2015 Jacobson SG, Cideciyan AV, Roman AJ, Sumaroka A, Schwartz SB, Heon E, Hauswirth WW. Improvement and decline in vision with gene therapy in childhood blindness. The New England Journal of Medicine. 372: 1920-6. PMID 25936984 DOI: 10.1056/Nejmoa1412965  0.036
1992 Schwartz SG. Holistic health: seeking a link between medicine and metaphysics. Jama. 266: 3064. PMID 1820484 DOI: 10.1001/jama.266.21.3064  0.035
2007 Aleman TS, Cideciyan AV, Windsor EA, Schwartz SB, Swider M, Chico JD, Sumaroka A, Pantelyat AY, Duncan KG, Gardner LM, Emmons JM, Steinberg JD, Stone EM, Jacobson SG. Macular pigment and lutein supplementation in ABCA4-associated retinal degenerations. Investigative Ophthalmology & Visual Science. 48: 1319-29. PMID 17325179 DOI: 10.1167/Iovs.06-0764  0.035
2014 Huang WC, Cideciyan AV, Roman AJ, Sumaroka A, Sheplock R, Schwartz SB, Stone EM, Jacobson SG. Inner and outer retinal changes in retinal degenerations associated with ABCA4 mutations. Investigative Ophthalmology & Visual Science. 55: 1810-22. PMID 24550365 DOI: 10.1167/Iovs.13-13768  0.033
2015 Cideciyan AV, Aguirre GK, Jacobson SG, Butt OH, Schwartz SB, Swider M, Roman AJ, Sadigh S, Hauswirth WW. Pseudo-fovea formation after gene therapy for RPE65-LCA. Investigative Ophthalmology & Visual Science. 56: 526-37. PMID 25537204 DOI: 10.1167/Iovs.14-15895  0.033
2010 Jacobson SG, Roman AJ, Aleman TS, Sumaroka A, Herrera W, Windsor EA, Atkinson LA, Schwartz SB, Steinberg JD, Cideciyan AV. Normal central retinal function and structure preserved in retinitis pigmentosa. Investigative Ophthalmology & Visual Science. 51: 1079-85. PMID 19797198 DOI: 10.1167/iovs.09-4372  0.033
2008 Aleman TS, Cideciyan AV, Sumaroka A, Windsor EA, Herrera W, White DA, Kaushal S, Naidu A, Roman AJ, Schwartz SB, Stone EM, Jacobson SG. Retinal laminar architecture in human retinitis pigmentosa caused by Rhodopsin gene mutations. Investigative Ophthalmology & Visual Science. 49: 1580-90. PMID 18385078 DOI: 10.1167/Iovs.07-1110  0.032
2003 Schwartz SB, Aleman TS, Cideciyan AV, Swaroop A, Jacobson SG, Stone EM. De novo mutation in the RP1 gene (Arg677ter) associated with retinitis pigmentosa. Investigative Ophthalmology & Visual Science. 44: 3593-7. PMID 12882812 DOI: 10.1167/Iovs.03-0155  0.029
2007 Kirwin SM, Vinette KM, Schwartz SB, Funanage VL, Gonzalez IL. Multiple transmissions of Barth syndrome through an oocyte donor with a de novo TAZ mutation. Fertility and Sterility. 87: 976.e5-7. PMID 17241629 DOI: 10.1016/j.fertnstert.2006.07.1543  0.028
2014 Schwartz S. Maternal placentophagy as an alternative medicinal practice in the postpartum period. Midwifery Today With International Midwife. 28-9. PMID 25112065  0.027
2011 Zelinger L, Banin E, Obolensky A, Mizrahi-Meissonnier L, Beryozkin A, Bandah-Rozenfeld D, Frenkel S, Ben-Yosef T, Merin S, Schwartz SB, Cideciyan AV, Jacobson SG, Sharon D. A missense mutation in DHDDS, encoding dehydrodolichyl diphosphate synthase, is associated with autosomal-recessive retinitis pigmentosa in Ashkenazi Jews. American Journal of Human Genetics. 88: 207-15. PMID 21295282 DOI: 10.1016/j.ajhg.2011.01.002  0.025
2015 Matsui R, Cideciyan AV, Schwartz SB, Sumaroka A, Roman AJ, Swider M, Huang WC, Sheplock R, Jacobson SG. Molecular Heterogeneity Within the Clinical Diagnosis of Pericentral Retinal Degeneration. Investigative Ophthalmology & Visual Science. 56: 6007-18. PMID 26393467 DOI: 10.1167/iovs.15-17174  0.024
2009 Schwartz S. Young cervical cancer patients and fertility. Seminars in Oncology Nursing. 25: 259-67. PMID 19879432 DOI: 10.1016/j.soncn.2009.08.003  0.02
2015 Chang AK, Foca M, Jin Z, Laird V, Schwartz S, Satwani P. The Significance of Daily Blood Cultures in Febrile Pediatric Hematopoietic Cell Transplant Recipients Biology of Blood and Marrow Transplantation. 21: S276. DOI: 10.1016/J.Bbmt.2014.11.436  0.019
2022 Geyer O, Ben-Shaul O, Lux C, Schwartz S, Podkovyrin O, Stein N, Lavi I, Mathalone N. Effect of Femtosecond Laser Cataract Surgery on Peripapillary Retinal Nerve Fiber Layer Thickness. Journal of Glaucoma. 31: 340-345. PMID 35302537 DOI: 10.1097/IJG.0000000000002014  0.013
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