| Year |
Citation |
Score |
| 2024 |
Lee PC, Jung IH, Thussu S, Patel V, Wagoner R, Burks KH, Amrute J, Elenbaas JS, Kang CJ, Young EP, Scherer PE, Stitziel NO. Instrumental variable and colocalization analyses identify endotrophin and HTRA1 as potential therapeutic targets for coronary artery disease. Iscience. 27: 110104. PMID 38989470 DOI: 10.1016/j.isci.2024.110104 |
0.368 |
|
| 2023 |
de Vries PS, Conomos MP, Singh K, Nicholson CJ, Jain D, Hasbani NR, Jiang W, Lee S, Cardenas CLL, Lutz SM, Wong D, Guo X, Yao J, Young EP, Tcheandjieu C, ... ... Stitziel NO, et al. Whole-genome sequencing uncovers two loci for coronary artery calcification and identifies ARSE as a regulator of vascular calcification. Nature Cardiovascular Research. 2: 1159-1172. PMID 38817323 DOI: 10.1038/s44161-023-00375-y |
0.31 |
|
| 2022 |
Yin X, Chan LS, Bose D, Jackson AU, VandeHaar P, Locke AE, Fuchsberger C, Stringham HM, Welch R, Yu K, Fernandes Silva L, Service SK, Zhang D, Hector EC, Young E, ... ... Stitziel NO, et al. Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Nature Communications. 13: 1644. PMID 35347128 DOI: 10.1038/s41467-022-29143-5 |
0.305 |
|
| 2021 |
Chen L, Abel HJ, Das I, Larson DE, Ganel L, Kanchi KL, Regier AA, Young EP, Kang CJ, Scott AJ, Chiang C, Wang X, Lu S, Christ R, Service SK, ... ... Stitziel NO, et al. Association of structural variation with cardiometabolic traits in Finns. American Journal of Human Genetics. 108: 583-596. PMID 33798444 DOI: 10.1016/j.ajhg.2021.03.008 |
0.303 |
|
| 2020 |
Chun S, Imakaev M, Hui D, Patsopoulos NA, Neale BM, Kathiresan S, Stitziel NO, Sunyaev SR. Non-parametric Polygenic Risk Prediction via Partitioned GWAS Summary Statistics. American Journal of Human Genetics. PMID 32470373 DOI: 10.1016/J.Ajhg.2020.05.004 |
0.382 |
|
| 2019 |
Evans TD, Zhang X, Clark RE, Alisio A, Song E, Zhang H, Reilly MP, Stitziel NO, Razani B. Functional Characterization of LIPA (Lysosomal Acid Lipase) Variants Associated With Coronary Artery Disease. Arteriosclerosis, Thrombosis, and Vascular Biology. ATVBAHA119313443. PMID 31645127 DOI: 10.1161/Atvbaha.119.313443 |
0.419 |
|
| 2019 |
Tabassum R, Rämö JT, Ripatti P, Koskela JT, Kurki M, Karjalainen J, Palta P, Hassan S, Nunez-Fontarnau J, Kiiskinen TTJ, Söderlund S, Matikainen N, Gerl MJ, Surma MA, Klose C, ... Stitziel NO, et al. Genetic architecture of human plasma lipidome and its link to cardiovascular disease. Nature Communications. 10: 4329. PMID 31551469 DOI: 10.1038/S41467-019-11954-8 |
0.389 |
|
| 2019 |
Locke AE, Steinberg KM, Chiang CWK, Service SK, Havulinna AS, Stell L, Pirinen M, Abel HJ, Chiang CC, Fulton RS, Jackson AU, Kang CJ, Kanchi KL, Koboldt DC, Larson DE, ... ... Stitziel NO, et al. Exome sequencing of Finnish isolates enhances rare-variant association power. Nature. PMID 31367044 DOI: 10.1038/S41586-019-1457-Z |
0.382 |
|
| 2019 |
Rämö JT, Ripatti P, Tabassum R, Söderlund S, Matikainen N, Gerl MJ, Klose C, Surma MA, Stitziel NO, Havulinna AS, Pirinen M, Salomaa V, Freimer NB, Jauhiainen M, Palotie A, et al. Coronary Artery Disease Risk and Lipidomic Profiles Are Similar in Hyperlipidemias With Family History and Population-Ascertained Hyperlipidemias. Journal of the American Heart Association. 8: e012415. PMID 31256696 DOI: 10.1161/Jaha.119.012415 |
0.38 |
|
| 2019 |
Lee VS, Halabi CM, Broekelmann TJ, Trackman PC, Stitziel NO, Mecham RP. Intracellular retention of mutant lysyl oxidase leads to aortic dilation in response to increased hemodynamic stress. Jci Insight. 5. PMID 31211696 DOI: 10.1172/Jci.Insight.127748 |
0.307 |
|
| 2019 |
Rämö J, Ripatti P, Tabassum R, Söderlund S, Matikainen N, Gerl MJ, Klose C, Surma M, Stitziel NO, Havulinna AS, Salomaa V, Freimer NB, Jauhiainen M, Palotie A, Taskinen M, et al. CORONARY ARTERY DISEASE RISK AND LIPIDOMIC PROFILES IN FAMILIAL HYPERLIPIDEMIAS Journal of the American College of Cardiology. 73: 1770. DOI: 10.1016/S0735-1097(19)32376-9 |
0.376 |
|
| 2019 |
Tabassum R, Rämö JT, Ripatti P, Koskela JT, Kurki M, Karjalainen J, Palta P, Hassan S, Nunez-Fontarnau J, Kiiskinen TTJ, Söderlund S, Matikainen N, Gerl MJ, Surma MA, Klose C, ... Stitziel NO, et al. Genetics Of Human Plasma Lipidome And Its Link To Diseases Susceptibility Atherosclerosis. 287. DOI: 10.1016/J.Atherosclerosis.2019.06.040 |
0.345 |
|
| 2018 |
Young EP, Stitziel NO. Capitalizing on Insights from Human Genetics to Identify Novel Therapeutic Targets for Coronary Artery Disease. Annual Review of Medicine. PMID 30355262 DOI: 10.1146/Annurev-Med-041717-085853 |
0.432 |
|
| 2018 |
Haghighi A, Krier JB, Toth-Petroczy A, Cassa CA, Frank NY, Carmichael N, Fieg E, Bjonnes A, Mohanty A, Briere LC, Lincoln S, Lucia S, Gupta VA, Söylemez O, Sutti S, ... ... Stitziel NO, et al. An integrated clinical program and crowdsourcing strategy for genomic sequencing and Mendelian disease gene discovery. Npj Genomic Medicine. 3: 21. PMID 30131872 DOI: 10.1038/S41525-018-0060-9 |
0.373 |
|
| 2018 |
Sturm AC, Knowles JW, Gidding SS, Ahmad ZS, Ahmed CD, Ballantyne CM, Baum SJ, Bourbon M, Carrié A, Cuchel M, de Ferranti SD, Defesche JC, Freiberger T, Hershberger RE, Hovingh GK, ... ... Stitziel NO, et al. Clinical Genetic Testing for Familial Hypercholesterolemia: JACC Scientific Expert Panel. Journal of the American College of Cardiology. 72: 662-680. PMID 30071997 DOI: 10.1016/J.Jacc.2018.05.044 |
0.375 |
|
| 2018 |
Lin CJ, Lin CY, Stitziel NO. Genetics of the extracellular matrix in aortic aneurysmal diseases. Matrix Biology : Journal of the International Society For Matrix Biology. PMID 29656146 DOI: 10.1016/J.Matbio.2018.04.005 |
0.301 |
|
| 2018 |
Elbitar S, Susan-Resiga D, Ghaleb Y, El Khoury P, Peloso G, Stitziel N, Rabès JP, Carreau V, Hamelin J, Ben-Djoudi-Ouadda A, Bruckert E, Boileau C, Seidah NG, Varret M, Abifadel M. New Sequencing technologies help revealing unexpected mutations in Autosomal Dominant Hypercholesterolemia. Scientific Reports. 8: 1943. PMID 29386597 DOI: 10.1038/S41598-018-20281-9 |
0.389 |
|
| 2017 |
Liu DJ, Peloso GM, Yu H, Butterworth AS, Wang X, Mahajan A, Saleheen D, Emdin C, Alam D, Alves AC, Amouyel P, Di Angelantonio E, Arveiler D, Assimes TL, Auer PL, ... ... Stitziel N, et al. Exome-wide association study of plasma lipids in >300,000 individuals. Nature Genetics. PMID 29083408 DOI: 10.1038/Ng.3977 |
0.375 |
|
| 2017 |
Emdin CA, Khera AV, Klarin D, Natarajan P, Zekavat SM, Nomura A, Haas ME, Aragam K, Ardissino D, Wilson JG, Schunkert H, McPherson R, Watkins H, Elosua R, Bown MJ, ... ... Stitziel N, et al. Phenotypic Consequences of a Genetic Predisposition to Enhanced Nitric Oxide Signaling. Circulation. PMID 28982690 DOI: 10.1161/Circulationaha.117.028021 |
0.417 |
|
| 2017 |
Auer PL, Stitziel NO. Genetic association studies in cardiovascular diseases: Do we have enough power? Trends in Cardiovascular Medicine. PMID 28456354 DOI: 10.1016/J.Tcm.2017.03.005 |
0.406 |
|
| 2017 |
Stitziel NO, Khera AV, Wang X, Bierhals AJ, Vourakis AC, Sperry AE, Natarajan P, Klarin D, Emdin CA, Zekavat SM, Nomura A, Erdmann J, Schunkert H, Samani NJ, Kraus WE, et al. ANGPTL3 Deficiency and Protection Against Coronary Artery Disease. Journal of the American College of Cardiology. PMID 28385496 DOI: 10.1016/J.Jacc.2017.02.030 |
0.411 |
|
| 2017 |
Khera AV, Won HH, Peloso GM, O'Dushlaine C, Liu D, Stitziel NO, Natarajan P, Nomura A, Emdin CA, Gupta N, Borecki IB, Asselta R, Duga S, Merlini PA, Correa A, et al. Association of Rare and Common Variation in the Lipoprotein Lipase Gene With Coronary Artery Disease. Jama. 317: 937-946. PMID 28267856 DOI: 10.1001/Jama.2017.0972 |
0.428 |
|
| 2017 |
Natarajan P, Young R, Stitziel NO, Padmanabhan S, Baber U, Mehran R, Sartori S, Fuster V, Reilly DF, Butterworth AS, Rader DJ, Ford I, Sattar N, Kathiresan S. Polygenic Risk Score Identifies Subgroup with Higher Burden of Atherosclerosis and Greater Relative Benefit from Statin Therapy in the Primary Prevention Setting. Circulation. PMID 28223407 DOI: 10.1161/Circulationaha.116.024436 |
0.375 |
|
| 2017 |
Webb TR, Erdmann J, Stirrups KE, Stitziel NO, Masca NG, Jansen H, Kanoni S, Nelson CP, Ferrario PG, König IR, Eicher JD, Johnson AD, Hamby SE, Betsholtz C, Ruusalepp A, et al. Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease. Journal of the American College of Cardiology. 69: 823-836. PMID 28209224 DOI: 10.1016/J.Jacc.2016.11.056 |
0.424 |
|
| 2017 |
Stitziel NO. Human genetic insights into lipoproteins and risk of cardiometabolic disease. Current Opinion in Lipidology. PMID 28059951 DOI: 10.1097/Mol.0000000000000389 |
0.414 |
|
| 2016 |
Stitziel NO. Variants in ANGPTL4 and the Risk of Coronary Artery Disease. The New England Journal of Medicine. 375: 2306. PMID 28112900 DOI: 10.1056/Nejmc1607380 |
0.381 |
|
| 2016 |
Emdin CA, Khera AV, Natarajan P, Klarin D, Won HH, Peloso GM, Stitziel NO, Nomura A, Zekavat SM, Bick AG, Gupta N, Asselta R, Duga S, Merlini PA, Correa A, et al. Phenotypic Characterization of Genetically Lowered Human Lipoprotein(a) Levels. Journal of the American College of Cardiology. 68: 2761-2772. PMID 28007139 DOI: 10.1016/J.Jacc.2016.10.033 |
0.428 |
|
| 2016 |
Gregson JM, Freitag DF, Surendran P, Stitziel NO, Chowdhury R, Burgess S, Kaptoge S, Gao P, Staley JR, Willeit P, Nielsen SF, Caslake M, Trompet S, Polfus LM, Kuulasmaa K, et al. Genetic invalidation of Lp-PLA2 as a therapeutic target: Large-scale study of five functional Lp-PLA2-lowering alleles. European Journal of Preventive Cardiology. PMID 27940953 DOI: 10.1177/2047487316682186 |
0.343 |
|
| 2016 |
Natarajan P, Bis JC, Bielak LF, Cox AJ, Dörr M, Feitosa MF, Franceschini N, Guo X, Hwang SJ, Isaacs A, Jhun MA, Kavousi M, Li-Gao R, Lyytikäinen LP, Marioni RE, ... ... Stitziel NO, et al. Multiethnic Exome-Wide Association Study of Subclinical Atherosclerosis. Circulation. Cardiovascular Genetics. PMID 27872105 DOI: 10.1161/Circgenetics.116.001572 |
0.45 |
|
| 2016 |
Stitziel NO, Kathiresan S. Leveraging human genetics to guide drug target discovery. Trends in Cardiovascular Medicine. PMID 27686272 DOI: 10.1016/J.Tcm.2016.08.008 |
0.383 |
|
| 2016 |
Liu C, Kraja AT, Smith JA, Brody JA, Franceschini N, Bis JC, Rice K, Morrison AC, Lu Y, Weiss S, Guo X, Palmas W, Martin LW, Chen YI, Surendran P, ... ... Stitziel NO, et al. Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci. Nature Genetics. PMID 27618448 DOI: 10.1038/Ng.3660 |
0.384 |
|
| 2016 |
Sommerville RB, Vincenti MG, Winborn K, Casey A, Stitziel NO, Connolly AM, Mann DL. Diagnosis and management of adult hereditary cardio-neuromuscular disorders: A model for the multidisciplinary care of complex genetic disorders. Trends in Cardiovascular Medicine. PMID 27452966 DOI: 10.1016/J.Tcm.2016.06.005 |
0.311 |
|
| 2016 |
Lee VS, Halabi CM, Hoffman EP, Carmichael N, Leshchiner I, Lian CG, Bierhals AJ, Vuzman D, Mecham RP, Frank NY, Stitziel NO. Loss of function mutation in LOX causes thoracic aortic aneurysm and dissection in humans. Proceedings of the National Academy of Sciences of the United States of America. PMID 27432961 DOI: 10.1073/Pnas.1601442113 |
0.382 |
|
| 2016 |
Golbus JR, Stitziel NO, Zhao W, Xue C, Farrall M, McPherson R, Erdmann J, Deloukas P, Watkins H, Schunkert H, Samani NJ, Saleheen D, Kathiresan S, Reilly MP. Common and Rare Genetic Variation in CCR2, CCR5, or CX3CR1 and Risk of Atherosclerotic Coronary Heart Disease and Glucometabolic Traits. Circulation. Cardiovascular Genetics. PMID 27013693 DOI: 10.1161/Circgenetics.115.001374 |
0.466 |
|
| 2016 |
Stitziel NO, Stirrups KE, Masca NGD, Erdmann J, Ferrario PG, Koenig IR, Weeke PE, Webb TR, Auer PL, Schick UM, Lu Y, Zhang H, Dube M, Goel A, Farrall M, et al. Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease (vol 374, pg 1134, 2016) The New England Journal of Medicine. 374: 1898-1898. DOI: 10.17863/Cam.15756 |
0.362 |
|
| 2016 |
Golbus JR, Stitziel N, Samani N, Erdmann J, Schunkert H, Deloukas P, Saleheen D, Farrall M, McPherson R, Watkins H, Kathiresan S, Reilly M. Common Or Rare Genetic Variation In The Chemokine Receptors Ccr2, Ccr5, And Cx3Cr1 Does Not Relate To Coronary Heart Disease Or Myocardial Infarction In Humans Journal of the American College of Cardiology. 67: 1891-1891. DOI: 10.1016/S0735-1097(16)31892-7 |
0.373 |
|
| 2015 |
Chopra SS, Leshchiner I, Duzkale H, McLaughlin H, Giovanni M, Zhang C, Stitziel N, Fingeroth J, Joyce RM, Lebo M, Rehm H, Vuzman D, Maas R, Sunyaev SR, Murray M, et al. Inherited CHST11/MIR3922 deletion is associated with a novel recessive syndrome presenting with skeletal malformation and malignant lymphoproliferative disease. Molecular Genetics & Genomic Medicine. 3: 413-23. PMID 26436107 DOI: 10.1002/Mgg3.152 |
0.308 |
|
| 2015 |
Olfson E, Cottrell CE, Davidson NO, Gurnett CA, Heusel JW, Stitziel NO, Chen LS, Hartz S, Nagarajan R, Saccone NL, Bierut LJ. Identification of Medically Actionable Secondary Findings in the 1000 Genomes. Plos One. 10: e0135193. PMID 26332594 DOI: 10.1371/Journal.Pone.0135193 |
0.409 |
|
| 2015 |
Mega JL, Stitziel NO, Smith JG, Chasman DI, Caulfield MJ, Devlin JJ, Nordio F, Hyde CL, Cannon CP, Sacks FM, Poulter NR, Sever PS, Ridker PM, Braunwald E, Melander O, et al. Genetic risk, coronary heart disease events, and the clinical benefit of statin therapy: an analysis of primary and secondary prevention trials. Lancet (London, England). 385: 2264-71. PMID 25748612 DOI: 10.1016/S0140-6736(14)61730-X |
0.424 |
|
| 2015 |
Stitziel NO, Peloso GM, Abifadel M, Cefalu AB, Fouchier S, Motazacker MM, Tada H, Larach DB, Awan Z, Haller JF, Pullinger CR, Varret M, Rabès JP, Noto D, Tarugi P, et al. Exome sequencing in suspected monogenic dyslipidemias. Circulation. Cardiovascular Genetics. 8: 343-50. PMID 25632026 DOI: 10.1161/Circgenetics.114.000776 |
0.318 |
|
| 2015 |
Do R, Stitziel NO, Won HH, Jørgensen AB, Duga S, Angelica Merlini P, Kiezun A, Farrall M, Goel A, Zuk O, Guella I, Asselta R, Lange LA, Peloso GM, Auer PL, et al. Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction. Nature. 518: 102-6. PMID 25487149 DOI: 10.1038/Nature13917 |
0.409 |
|
| 2015 |
Schick UM, Auer PL, Bis JC, Lin H, Wei P, Pankratz N, Lange LA, Brody J, Stitziel NO, Kim DS, Carlson CS, Fornage M, Haessler J, Hsu L, Jackson RD, et al. Association of exome sequences with plasma C-reactive protein levels in >9000 participants. Human Molecular Genetics. 24: 559-71. PMID 25187575 DOI: 10.1093/Hmg/Ddu450 |
0.402 |
|
| 2014 |
Stitziel NO, Won HH, Morrison AC, Peloso GM, Do R, Lange LA, Fontanillas P, Gupta N, Duga S, Goel A, Farrall M, Saleheen D, Ferrario P, König I, et al. Inactivating mutations in NPC1L1 and protection from coronary heart disease. The New England Journal of Medicine. 371: 2072-82. PMID 25390462 DOI: 10.1056/Nejmoa1405386 |
0.386 |
|
| 2014 |
Stitziel NO, MacRae CA. A clinical approach to inherited premature coronary artery disease. Circulation. Cardiovascular Genetics. 7: 558-64. PMID 25140063 DOI: 10.1161/Circgenetics.113.000152 |
0.416 |
|
| 2014 |
Lim ET, Würtz P, Havulinna AS, Palta P, Tukiainen T, Rehnström K, Esko T, Mägi R, Inouye M, Lappalainen T, Chan Y, Salem RM, Lek M, Flannick J, Sim X, ... ... Stitziel NO, et al. Distribution and medical impact of loss-of-function variants in the Finnish founder population. Plos Genetics. 10: e1004494. PMID 25078778 DOI: 10.1371/Journal.Pgen.1004494 |
0.43 |
|
| 2014 |
Crosby J, Peloso GM, Auer PL, Crosslin DR, Stitziel NO, Lange LA, Lu Y, Tang ZZ, Zhang H, Hindy G, Masca N, Stirrups K, Kanoni S, Do R, et al. Loss-of-function mutations in APOC3, triglycerides, and coronary disease. The New England Journal of Medicine. 371: 22-31. PMID 24941081 DOI: 10.1056/Nejmoa1307095 |
0.421 |
|
| 2014 |
Brownstein CA, Beggs AH, Homer N, Merriman B, Yu TW, Flannery KC, DeChene ET, Towne MC, Savage SK, Price EN, Holm IA, Luquette LJ, Lyon E, Majzoub J, Neupert P, ... ... Stitziel NO, et al. An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge. Genome Biology. 15: R53. PMID 24667040 DOI: 10.1186/Gb-2014-15-3-R53 |
0.371 |
|
| 2014 |
Peloso GM, Auer PL, Bis JC, Voorman A, Morrison AC, Stitziel NO, Brody JA, Khetarpal SA, Crosby JR, Fornage M, Isaacs A, Jakobsdottir J, Feitosa MF, Davies G, Huffman JE, et al. Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks. American Journal of Human Genetics. 94: 223-32. PMID 24507774 DOI: 10.1016/J.Ajhg.2014.01.009 |
0.368 |
|
| 2014 |
Natarajan P, Stitziel N, Ferencik M, Hildebrand L, Gupta N, Gabriel S, Hoffmann U, Kathiresan S. Coronary Computed Tomography Angiography And Whole Genome Sequencing As An Approach To Discover The Genetic Basis Of Disease In A Family Prone To Myocardial Infarction Journal of the American College of Cardiology. 63. DOI: 10.1016/S0735-1097(14)61563-1 |
0.392 |
|
| 2014 |
Martinez S, Lenzini P, Stitziel N, Kathiresan S, Spertus J, Cresci S. Post-Myocardial Infarction Mortality Is Associated With A Genetic Risk Score Journal of the American College of Cardiology. 63. DOI: 10.1016/S0735-1097(14)60012-7 |
0.438 |
|
| 2014 |
Fouchier SW, Stitziel NO, Dallinga-Thie GM, Meijers JCM, Zelcer N, Kastelein JJP, Defesche JC, Kathiresan S, Hovingh GK. Mutations in stap1 are associated with autosomal dominant hypercholesterolemia Atherosclerosis. 235. DOI: 10.1016/J.Atherosclerosis.2014.05.019 |
0.308 |
|
| 2013 |
Awan Z, Choi HY, Stitziel N, Ruel I, Bamimore MA, Husa R, Gagnon MH, Wang RH, Peloso GM, Hegele RA, Seidah NG, Kathiresan S, Genest J. APOE p.Leu167del mutation in familial hypercholesterolemia. Atherosclerosis. 231: 218-22. PMID 24267230 DOI: 10.1016/J.Cjca.2013.07.652 |
0.366 |
|
| 2013 |
Stitziel NO, Fouchier SW, Sjouke B, Peloso GM, Moscoso AM, Auer PL, Goel A, Gigante B, Barnes TA, Melander O, Orho-Melander M, Duga S, Sivapalaratnam S, Nikpay M, Martinelli N, et al. Exome sequencing and directed clinical phenotyping diagnose cholesterol ester storage disease presenting as autosomal recessive hypercholesterolemia. Arteriosclerosis, Thrombosis, and Vascular Biology. 33: 2909-14. PMID 24072694 DOI: 10.1161/Atvbaha.113.302426 |
0.386 |
|
| 2013 |
Minicocci I, Santini S, Cantisani V, Stitziel N, Kathiresan S, Arroyo JA, Martí G, Pisciotta L, Noto D, Cefalù AB, Maranghi M, Labbadia G, Pigna G, Pannozzo F, Ceci F, et al. Clinical characteristics and plasma lipids in subjects with familial combined hypolipidemia: A pooled analysis Journal of Lipid Research. 54: 3481-3490. PMID 24058201 DOI: 10.1194/Jlr.P039875 |
0.368 |
|
| 2012 |
Kiezun A, Garimella K, Do R, Stitziel NO, Neale BM, McLaren PJ, Gupta N, Sklar P, Sullivan PF, Moran JL, Hultman CM, Lichtenstein P, Magnusson P, Lehner T, Shugart YY, et al. Exome sequencing and the genetic basis of complex traits. Nature Genetics. 44: 623-30. PMID 22641211 DOI: 10.1038/Ng.2303 |
0.347 |
|
| 2012 |
Stitziel NO. Rare Coding Mutations And Risk For Early-Onset Myocardial Infarction: An Exome Sequencing Study Of >2,000 Cases And Controls Journal of the American College of Cardiology. 59. DOI: 10.1016/S0735-1097(12)60436-7 |
0.372 |
|
| 2011 |
Stitziel NO, Kiezun A, Sunyaev S. Computational and statistical approaches to analyzing variants identified by exome sequencing Genome Biology. 12. PMID 21920052 DOI: 10.1186/Gb-2011-12-9-227 |
0.342 |
|
| 2004 |
Stitziel NO, Mar BG, Liang J, Westbrook CA. Membrane-associated and secreted genes in breast cancer. Cancer Research. 64: 8682-7. PMID 15574777 DOI: 10.1158/0008-5472.Can-04-1729 |
0.571 |
|
| 2004 |
Stitziel NO, Binkowski TA, Tseng YY, Kasif S, Liang J. topoSNP: a topographic database of non-synonymous single nucleotide polymorphisms with and without known disease association. Nucleic Acids Research. 32: D520-2. PMID 14681472 DOI: 10.1093/Nar/Gkh104 |
0.307 |
|
| 2003 |
Stitziel NO, Tseng YY, Pervouchine D, Goddeau D, Kasif S, Liang J. Structural location of disease-associated single-nucleotide polymorphisms. Journal of Molecular Biology. 327: 1021-30. PMID 12662927 DOI: 10.1016/S0022-2836(03)00240-7 |
0.354 |
|
| 1999 |
Marth GT, Korf I, Yandell MD, Yeh RT, Gu Z, Zakeri H, Stitziel NO, Hillier L, Kwok PY, Gish WR. A general approach to single-nucleotide polymorphism discovery. Nature Genetics. 23: 452-6. PMID 10581034 DOI: 10.1038/70570 |
0.332 |
|
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