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Nadia Solovieff, Ph.D. - Publications

Affiliations: 
2011 Boston University, Boston, MA, United States 
Area:
Statistics, Epidemiology, Genetics
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38 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, 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
2020 Andre F, Su F, Solovieff N, Arteaga CL, Hortobagyi GN, Chia SKL, Neven P, Bardia A, Tripathy D, Lu Y, Wang Y, Rodriguez-Lorenc K, Taran T, Babbar N, Slamon DJ. Pooled ctDNA analysis of the MONALEESA (ML) phase III advanced breast cancer (ABC) trials. Journal of Clinical Oncology. 38: 1009-1009. DOI: 10.1200/Jco.2020.38.15_Suppl.1009  0.336
2019 Neven P, Petrakova K, Bianchi GV, Cruz-Merino LDl, Jerusalem G, Sonke G, Nusch A, Beck J, Chia S, Solovieff N, Lorenc KR, Miller M, Su F, Lm S. Abstract PD2-05: Biomarker analysis by baseline circulating tumor DNA alterations in the MONALEESA-3 study Cancer Research. 79. DOI: 10.1158/1538-7445.Sabcs18-Pd2-05  0.341
2019 Yap Y, Su F, Solovieff N, Ito Y, Masuda N, Ishikawa T, Aruga T, Kim SJ, He W, Gazdoiu M, Chiu J. Abstract CT143: Baseline circulating tumor DNA (ctDNA) analysis in Asian women with HR+/HER2- advanced breast cancer (ABC) receiving ribociclib + endocrine therapy in the Phase Ib MONALEESASIA trial Cancer Research. 79. DOI: 10.1158/1538-7445.Am2019-Ct143  0.34
2019 Bardia A, Su F, Solovieff N, Im S, Sohn J, Lee KS, Campos-Gomez S, Jung KH, Vazquez RV, Lu Y, Franke F, Hurvitz S, Harbeck N, Chow L, Lorenc KR, et al. Abstract CT141: Genetic landscape of premenopausal HR+/HER2- advanced breast cancer (ABC) based on comprehensive circulating tumor DNA analysis and association with clinical outcomes in the Phase III MONALEESA-7 trial Cancer Research. 79. DOI: 10.1158/1538-7445.Am2019-Ct141  0.369
2019 Solovieff N, Su F, Leary R, Balbin A, Chakravartty A, Lorenc KR, Taran T, Babbar N. Abstract A031: Association of tumor DNA in circulation with clinical characteristics and treatment response in HR+/HER2− advanced breast cancer Molecular Cancer Therapeutics. 18. DOI: 10.1158/1535-7163.Targ-19-A031  0.303
2018 Hortobagyi G, Stemmer S, Campone M, Sonke G, Arteaga C, Paluch-Shimon S, Petrakova K, Villanueva C, Nusch A, Grischke E, Chan A, Jakobsen E, Marschner N, Hart L, Alba E, ... ... Solovieff N, et al. Abstract PD4-06: First-line ribociclib + letrozole in hormone receptor-positive, HER2-negative advanced breast cancer: Efficacy by baseline circulating tumor DNA alterations in MONALEESA-2 Cancer Research. 78. DOI: 10.1158/1538-7445.Sabcs17-Pd4-06  0.305
2018 Solovieff N, Wang YA, Sankaran B, Scheuer N, El-Hashimy M, Weber D, Sellami D, Leo AD. Abstract A029: Biomarker analysis in HR+, HER2-, locally advanced, or metastatic breast cancer patients treated with buparlisib: results from BELLE-3 Molecular Cancer Therapeutics. 17. DOI: 10.1158/1535-7163.Targ-17-A029  0.31
2015 Solovieff N, Singh AP, Bitter H, Riester M, Teneriello M, Oza A, Monk B, Robinson D, Trandafir L, Massacesi C, Tomaso Ed, Naumann RW. Abstract A02: Biomarkers of drug response to buparlisib: Results of next-generation sequencing in a phase II trial of advanced endometrial carcinoma Molecular Cancer Therapeutics. 14. DOI: 10.1158/1538-8514.Pi3K14-A02  0.315
2015 Solovieff N, Hims M, Leary R, Chiang D, Germa C, Massacesi C, Hirawat S, Scherer SJ, Morrissey M, Winckler W, Tomaso Ed. Abstract LB-A05: Profiling cell free DNA in breast cancer and non-small cell lung cancer using broad NGS assessment Molecular Cancer Therapeutics. 14. DOI: 10.1158/1535-7163.Targ-15-Lb-A05  0.304
2014 Guffanti G, Ashley-Koch AE, Roberts AL, Garrett ME, Solovieff N, Ratanatharathorn A, De Vivo I, Dennis M, Ranu H, Smoller JW, Liu Y, Purcell SM, Beckham J, Hauser MA, et al. No association between RORA polymorphisms and PTSD in two independent samples. Molecular Psychiatry. 19: 1056-7. PMID 25048002 DOI: 10.1038/Mp.2014.19  0.384
2014 Solovieff N, Roberts AL, Ratanatharathorn A, Haloosim M, De Vivo I, King AP, Liberzon I, Aiello A, Uddin M, Wildman DE, Galea S, Smoller JW, Purcell SM, Koenen KC. Genetic association analysis of 300 genes identifies a risk haplotype in SLC18A2 for post-traumatic stress disorder in two independent samples. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 39: 1872-9. PMID 24525708 DOI: 10.1038/Npp.2014.34  0.446
2014 Purcell SM, Moran JL, Fromer M, Ruderfer D, Solovieff N, Roussos P, O'Dushlaine C, Chambert K, Bergen SE, Kähler A, Duncan L, Stahl E, Genovese G, Fernández E, Collins MO, et al. A polygenic burden of rare disruptive mutations in schizophrenia. Nature. 506: 185-90. PMID 24463508 DOI: 10.1038/Nature12975  0.376
2013 Guffanti G, Galea S, Yan L, Roberts AL, Solovieff N, Aiello AE, Smoller JW, De Vivo I, Ranu H, Uddin M, Wildman DE, Purcell S, Koenen KC. Genome-wide association study implicates a novel RNA gene, the lincRNA AC068718.1, as a risk factor for post-traumatic stress disorder in women. Psychoneuroendocrinology. 38: 3029-38. PMID 24080187 DOI: 10.1016/J.Psyneuen.2013.08.014  0.352
2013 Solovieff N, Cotsapas C, Lee PH, Purcell SM, Smoller JW. Pleiotropy in complex traits: challenges and strategies. Nature Reviews. Genetics. 14: 483-95. PMID 23752797 DOI: 10.1038/Nrg3461  0.365
2013 Ngo D, Bae H, Steinberg MH, Sebastiani P, Solovieff N, Baldwin CT, Melista E, Safaya S, Farrer LA, Al-Suliman AM, Albuali WH, Al Bagshi MH, Naserullah Z, Akinsheye I, Gallagher P, et al. Fetal hemoglobin in sickle cell anemia: genetic studies of the Arab-Indian haplotype. Blood Cells, Molecules & Diseases. 51: 22-6. PMID 23465615 DOI: 10.1016/J.Bcmd.2012.12.005  0.715
2012 Alsultan A, Ngo DA, Farrell JJ, Akinsheye I, Solovieff N, Ghabbour HA, Al-Ali A, Alsuliman A, Al-Baghshi M, Albu-Ali W, Alabdulaali M, Baldwin CT, Farrer LA, Luo H, Melista E, et al. A functional promoter polymorphism of the δ-globin gene is a specific marker of the Arab-Indian haplotype. American Journal of Hematology. 87: 824-6. PMID 22641479 DOI: 10.1002/Ajh.23239  0.424
2012 Milton JN, Sebastiani P, Solovieff N, Hartley SW, Bhatnagar P, Arking DE, Dworkis DA, Casella JF, Barron-Casella E, Bean CJ, Hooper WC, DeBaun MR, Garrett ME, Soldano K, Telen MJ, et al. A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia. Plos One. 7: e34741. PMID 22558097 DOI: 10.1371/Journal.Pone.0034741  0.604
2012 Sebastiani P, Solovieff N, Sun JX. Naïve Bayesian Classifier and Genetic Risk Score for Genetic Risk Prediction of a Categorical Trait: Not so Different after all! Frontiers in Genetics. 3: 26. PMID 22393331 DOI: 10.3389/Fgene.2012.00026  0.535
2012 Conneely KN, Capell BC, Erdos MR, Sebastiani P, Solovieff N, Swift AJ, Baldwin CT, Budagov T, Barzilai N, Atzmon G, Puca AA, Perls TT, Geesaman BJ, Boehnke M, Collins FS. Human longevity and common variations in the LMNA gene: a meta-analysis. Aging Cell. 11: 475-81. PMID 22340368 DOI: 10.1111/J.1474-9726.2012.00808.X  0.572
2012 Sebastiani P, Solovieff N, Dewan AT, Walsh KM, Puca A, Hartley SW, Melista E, Andersen S, Dworkis DA, Wilk JB, Myers RH, Steinberg MH, Montano M, Baldwin CT, Hoh J, et al. Genetic signatures of exceptional longevity in humans. Plos One. 7: e29848. PMID 22279548 DOI: 10.1371/Journal.Pone.0029848  0.61
2012 Akinsheye I, Solovieff N, Ngo D, Malek A, Sebastiani P, Steinberg MH, Chui DH. Fetal hemoglobin in sickle cell anemia: molecular characterization of the unusually high fetal hemoglobin phenotype in African Americans. American Journal of Hematology. 87: 217-9. PMID 22139998 DOI: 10.1002/Ajh.22221  0.601
2012 Sebastiani P, Solovieff N, DeWan AT, Walsh KM, Puca A, Hartley SW, Melista E, Andersen S, Dworkis DA, Wilk JB, Myers RH, Steinberg MH, Montano M, Baldwin CT, Hoh J, et al. Example of 9 clusters of genetic risk profiles in centenarians of the discovery set and 3 similar clusters in replication sets 1 and 2. Plos One. DOI: 10.1371/Journal.Pone.0029848.G008  0.504
2011 Sebastiani P, Solovieff N, Puca A, Hartley SW, Melista E, Andersen S, Dworkis DA, Wilk JB, Myers RH, Steinberg MH, Montano M, Baldwin CT, Perls TT. Retraction. Science (New York, N.Y.). 333: 404. PMID 21778381 DOI: 10.1126/science.333.6041.404-a  0.338
2011 Alsultan A, Solovieff N, Aleem A, AlGahtani FH, Al-Shehri A, Osman ME, Kurban K, Bahakim H, Al-Momen AK, Baldwin CT, Chui DH, Steinberg MH. Fetal hemoglobin in sickle cell anemia: Saudi patients from the Southwestern province have similar HBB haplotypes but higher HbF levels than African Americans. American Journal of Hematology. 86: 612-4. PMID 21630302 DOI: 10.1002/Ajh.22032  0.498
2011 Solovieff N, Hartley SW, Baldwin CT, Klings ES, Gladwin MT, Taylor JG, Kato GJ, Farrer LA, Steinberg MH, Sebastiani P. Ancestry of African Americans with sickle cell disease. Blood Cells, Molecules & Diseases. 47: 41-5. PMID 21546286 DOI: 10.1016/J.Bcmd.2011.04.002  0.566
2011 Akinsheye I, Alsultan A, Solovieff N, Ngo D, Baldwin CT, Sebastiani P, Chui DH, Steinberg MH. Fetal hemoglobin in sickle cell anemia. Blood. 118: 19-27. PMID 21490337 DOI: 10.1182/Blood-2011-03-325258  0.588
2011 Dworkis DA, Klings ES, Solovieff N, Li G, Milton JN, Hartley SW, Melista E, Parente J, Sebastiani P, Steinberg MH, Baldwin CT. Severe sickle cell anemia is associated with increased plasma levels of TNF-R1 and VCAM-1. American Journal of Hematology. 86: 220-3. PMID 21264913 DOI: 10.1002/Ajh.21928  0.574
2011 Solovieff N, Steinberg MH, Sebastiani P. Genetic admixture in sickle cell disease Blood. 118: 4495. DOI: 10.1182/Blood-2011-09-373274  0.609
2011 Sebastiani P, Solovieff N, Puca A, Hartley SW, Melista E, Andersen S, Dworkis DA, Wilk JB, Myers RH, Steinberg MH, Montano M, Baldwin CT, Perls TT. Retraction (Science) Science. 333: 404.  0.35
2010 Solovieff N, Hartley SW, Baldwin CT, Perls TT, Steinberg MH, Sebastiani P. Clustering by genetic ancestry using genome-wide SNP data. Bmc Genetics. 11: 108. PMID 21143920 DOI: 10.1186/1471-2156-11-108  0.582
2010 Sebastiani P, Solovieff N, Puca A, Hartley SW, Melista E, Andersen S, Dworkis DA, Wilk JB, Myers RH, Steinberg MH, Montano M, Baldwin CT, Perls TT. Genetic signatures of exceptional longevity in humans. Science (New York, N.Y.). 2010. PMID 20595579 DOI: 10.1126/Science.1190532  0.619
2010 Sebastiani P, Solovieff N, Hartley SW, Milton JN, Riva A, Dworkis DA, Melista E, Klings ES, Garrett ME, Telen MJ, Ashley-Koch A, Baldwin CT, Steinberg MH. Genetic modifiers of the severity of sickle cell anemia identified through a genome-wide association study. American Journal of Hematology. 85: 29-35. PMID 20029952 DOI: 10.1002/Ajh.21572  0.632
2010 Solovieff N, Milton JN, Hartley SW, Sherva R, Sebastiani P, Dworkis DA, Klings ES, Farrer LA, Garrett ME, Ashley-Koch A, Telen MJ, Fucharoen S, Ha SY, Li CK, Chui DH, et al. Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster. Blood. 115: 1815-22. PMID 20018918 DOI: 10.1182/Blood-2009-08-239517  0.594
2010 Dworkis DA, Klings E, Solovieff N, Li G, Milton JN, Hartley SW, Melista E, Parente J, Sebastiani P, Steinberg MH, Baldwin CT. Tumor Necrosis Factor-α Signaling In Sickle Cell Disease: Elevated Biomarker Levels and Genetic Associations with Disease Severity Blood. 116: 2654-2654. DOI: 10.1182/Blood.V116.21.2654.2654  0.578
2010 Akinsheye I, Solovieff N, Malek A, Ngo DA, Steinberg MH, Chui DH. Fetal Hemoglobin In Sickle Cell Anemia: Molecular Characterization of the High Fetal Hemoglobin Phenotype In African American Patients Blood. 116: 2068-2068. DOI: 10.1182/Blood.V116.21.2068.2068  0.447
2010 Alsultan A, Solovieff N, Aleem A, AlGahtani FH, Al-Shehri A, Osman ME, Kurban K, Bahakim H, Al-Momen AK, Chui DH, Steinberg MH. Fetal Hemoglobin In Sickle Cell Anemia: Molecular Characterization of Saudi Patients From the Southwestern Province. Blood. 116: 1621-1621. DOI: 10.1182/Blood.V116.21.1621.1621  0.486
2009 Sebastiani P, Montano M, Puca A, Solovieff N, Kojima T, Wang MC, Melista E, Meltzer M, Fischer SE, Andersen S, Hartley SH, Sedgewick A, Arai Y, Bergman A, Barzilai N, et al. RNA editing genes associated with extreme old age in humans and with lifespan in C. elegans. Plos One. 4: e8210. PMID 20011587 DOI: 10.1371/Journal.Pone.0008210  0.584
2009 Sebastiani P, Montano M, Puca A, Solovieff N, Kojima T, Wang MC, Melista E, Meltzer M, Fischer SEJ, Andersen S, Hartley SH, Sedgewick A, Arai Y, Bergman A, Barzilai N, et al. Correction: RNA Editing Genes Associated with Extreme Old Age in Humans and with Lifespan in C. elegans Plos One. 4. DOI: 10.1371/Annotation/387F8074-5F80-4Bdd-Bb0B-B36D49A16Ac0  0.49
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