共 50 条
- [1] Identification of novel rare genetic variants associated with COPD in the general populationEUROPEAN RESPIRATORY JOURNAL, 2018, 52de Vries, Maaike论文数: 0 引用数: 0 h-index: 0机构: Univ Groningen, Univ Med Ctr Groningen, Dept Epidemiol, Groningen Res Inst Asthma & COPD GRIAC, Groningen, Netherlands Univ Groningen, Univ Med Ctr Groningen, Dept Epidemiol, Groningen Res Inst Asthma & COPD GRIAC, Groningen, NetherlandsVan der Plaat, Diana A.论文数: 0 引用数: 0 h-index: 0机构: Univ Groningen, Univ Med Ctr Groningen, Dept Epidemiol, Groningen Res Inst Asthma & COPD GRIAC, Groningen, Netherlands Univ Groningen, Univ Med Ctr Groningen, Dept Epidemiol, Groningen Res Inst Asthma & COPD GRIAC, Groningen, NetherlandsNedeljkovic, Ivana论文数: 0 引用数: 0 h-index: 0机构: Erasmus MC, Dept Epidemiol, Rotterdam, Netherlands Univ Groningen, Univ Med Ctr Groningen, Dept Epidemiol, Groningen Res Inst Asthma & COPD GRIAC, Groningen, NetherlandsVan der Velde, K. Joeri论文数: 0 引用数: 0 h-index: 0机构: Univ Groningen, Univ Med Ctr Groningen, Dept Genet, Groningen, Netherlands Univ Groningen, Univ Med Ctr Groningen, Dept Epidemiol, Groningen Res Inst Asthma & COPD GRIAC, Groningen, NetherlandsAmin, Najaf论文数: 0 引用数: 0 h-index: 0机构: Erasmus MC, Dept Epidemiol, Rotterdam, Netherlands Univ Groningen, Univ Med Ctr Groningen, Dept Epidemiol, Groningen Res Inst Asthma & COPD GRIAC, Groningen, NetherlandsVan Duijn, Cornelia论文数: 0 引用数: 0 h-index: 0机构: Erasmus MC, Dept Epidemiol, Rotterdam, Netherlands Univ Groningen, Univ Med Ctr Groningen, Dept Epidemiol, Groningen Res Inst Asthma & COPD GRIAC, Groningen, NetherlandsVonk, Judith M.论文数: 0 引用数: 0 h-index: 0机构: Univ Groningen, Univ Med Ctr Groningen, Dept Epidemiol, Groningen Res Inst Asthma & COPD GRIAC, Groningen, Netherlands Univ Groningen, Univ Med Ctr Groningen, Dept Epidemiol, Groningen Res Inst Asthma & COPD GRIAC, Groningen, NetherlandsBoezen, H. Marike论文数: 0 引用数: 0 h-index: 0机构: Univ Groningen, Univ Med Ctr Groningen, Dept Epidemiol, Groningen Res Inst Asthma & COPD GRIAC, Groningen, Netherlands Univ Groningen, Univ Med Ctr Groningen, Dept Epidemiol, Groningen Res Inst Asthma & COPD GRIAC, Groningen, NetherlandsVan Diemen, Cleo C.论文数: 0 引用数: 0 h-index: 0机构: Univ Groningen, Univ Med Ctr Groningen, Dept Genet, Groningen, Netherlands Univ Groningen, Univ Med Ctr Groningen, Dept Epidemiol, Groningen Res Inst Asthma & COPD GRIAC, Groningen, Netherlands
- [2] Identification of rare genetic variants associated with sporadic CJD by exome sequencingPRION, 2019, 13 : 58 - 59Speedy, Helen论文数: 0 引用数: 0 h-index: 0机构: UCL, UCL Inst Prion Dis, MRC Prion Unit, Courtauld Bldg, London, England UCL, UCL Inst Prion Dis, MRC Prion Unit, Courtauld Bldg, London, EnglandNorsworthy, Penny论文数: 0 引用数: 0 h-index: 0机构: UCL, UCL Inst Prion Dis, MRC Prion Unit, Courtauld Bldg, London, England UCL, UCL Inst Prion Dis, MRC Prion Unit, Courtauld Bldg, London, EnglandHummerich, Holger论文数: 0 引用数: 0 h-index: 0机构: UCL, UCL Inst Prion Dis, MRC Prion Unit, Courtauld Bldg, London, England UCL, UCL Inst Prion Dis, MRC Prion Unit, Courtauld Bldg, London, EnglandAdamson, Gary论文数: 0 引用数: 0 h-index: 0机构: UCL, UCL Inst Prion Dis, MRC Prion Unit, Courtauld Bldg, London, England UCL, UCL Inst Prion Dis, MRC Prion Unit, Courtauld Bldg, London, EnglandUphill, James论文数: 0 引用数: 0 h-index: 0机构: UCL, UCL Inst Prion Dis, MRC Prion Unit, Courtauld Bldg, London, England UCL, UCL Inst Prion Dis, MRC Prion Unit, Courtauld Bldg, London, EnglandCollinge, John论文数: 0 引用数: 0 h-index: 0机构: UCL, UCL Inst Prion Dis, MRC Prion Unit, Courtauld Bldg, London, England UCL, UCL Inst Prion Dis, MRC Prion Unit, Courtauld Bldg, London, EnglandMead, Simon论文数: 0 引用数: 0 h-index: 0机构: UCL, UCL Inst Prion Dis, MRC Prion Unit, Courtauld Bldg, London, England UCL, UCL Inst Prion Dis, MRC Prion Unit, Courtauld Bldg, London, England
- [3] Identification of genetic variants in pharmacokinetic genes associated with Ewing Sarcoma treatment outcomeANNALS OF ONCOLOGY, 2016, 27 (09) : 1788 - 1793Ruiz-Pinto, S.论文数: 0 引用数: 0 h-index: 0机构: Spanish Natl Canc Res Ctr CNIO, Human Genotyping Unit CeGen, Human Canc Genet Programme, Madrid, Spain Spanish Natl Canc Res Ctr CNIO, Human Genotyping Unit CeGen, Human Canc Genet Programme, Madrid, SpainPita, G.论文数: 0 引用数: 0 h-index: 0机构: Spanish Natl Canc Res Ctr CNIO, Human Genotyping Unit CeGen, Human Canc Genet Programme, Madrid, Spain Spanish Natl Canc Res Ctr CNIO, Human Genotyping Unit CeGen, Human Canc Genet Programme, Madrid, SpainPatino-Garcia, A.论文数: 0 引用数: 0 h-index: 0机构: CUN, Clin Genet Unit, Pamplona, Spain Spanish Natl Canc Res Ctr CNIO, Human Genotyping Unit CeGen, Human Canc Genet Programme, Madrid, SpainGarcia-Miguel, P.论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ La Paz, Dept Pediat Hematooncol, Madrid, Spain Spanish Natl Canc Res Ctr CNIO, Human Genotyping Unit CeGen, Human Canc Genet Programme, Madrid, SpainAlonso, J.论文数: 0 引用数: 0 h-index: 0机构: Inst Salud Carlos III, Res Inst Rare Dis, Dept Human Genet, Pediat Solid Tumor Lab, Madrid, Spain Spanish Natl Canc Res Ctr CNIO, Human Genotyping Unit CeGen, Human Canc Genet Programme, Madrid, SpainPerez-Martinez, A.论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ La Paz, Dept Pediat Hematooncol, Madrid, Spain Spanish Natl Canc Res Ctr CNIO, Human Genotyping Unit CeGen, Human Canc Genet Programme, Madrid, SpainSastre, A.论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ La Paz, Dept Pediat Hematooncol, Madrid, Spain Spanish Natl Canc Res Ctr CNIO, Human Genotyping Unit CeGen, Human Canc Genet Programme, Madrid, SpainGomez-Mariano, G.论文数: 0 引用数: 0 h-index: 0机构: Inst Salud Carlos III, Res Inst Rare Dis, Dept Human Genet, Pediat Solid Tumor Lab, Madrid, Spain Spanish Natl Canc Res Ctr CNIO, Human Genotyping Unit CeGen, Human Canc Genet Programme, Madrid, SpainLissat, A.论文数: 0 引用数: 0 h-index: 0机构: Charite, Div Hematol & Oncol, Dept Pediat, Berlin, Germany Spanish Natl Canc Res Ctr CNIO, Human Genotyping Unit CeGen, Human Canc Genet Programme, Madrid, SpainScotlandi, K.论文数: 0 引用数: 0 h-index: 0机构: Ist Ortoped Rizzoli, Expt Oncol Lab, Bologna, Italy Spanish Natl Canc Res Ctr CNIO, Human Genotyping Unit CeGen, Human Canc Genet Programme, Madrid, SpainSerra, M.论文数: 0 引用数: 0 h-index: 0机构: Ist Ortoped Rizzoli, Expt Oncol Lab, Bologna, Italy Spanish Natl Canc Res Ctr CNIO, Human Genotyping Unit CeGen, Human Canc Genet Programme, Madrid, SpainLadenstein, R.论文数: 0 引用数: 0 h-index: 0机构: Med Univ, St Anna Kinderkrebsforsch eV, Childrens Canc Res Inst, Dept Pediat, Vienna, Austria Spanish Natl Canc Res Ctr CNIO, Human Genotyping Unit CeGen, Human Canc Genet Programme, Madrid, SpainLapouble, E.论文数: 0 引用数: 0 h-index: 0机构: Inst Curie, Somat Genet Unit, Paris, France Spanish Natl Canc Res Ctr CNIO, Human Genotyping Unit CeGen, Human Canc Genet Programme, Madrid, SpainPierron, G.论文数: 0 引用数: 0 h-index: 0机构: Inst Curie, Somat Genet Unit, Paris, France Spanish Natl Canc Res Ctr CNIO, Human Genotyping Unit CeGen, Human Canc Genet Programme, Madrid, SpainKontny, U.论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr, Div Paediat Haematol Oncol & Stem Cell Transplant, Dept Paediat & Adolescent Med, Aachen, Germany Spanish Natl Canc Res Ctr CNIO, Human Genotyping Unit CeGen, Human Canc Genet Programme, Madrid, SpainPicci, P.论文数: 0 引用数: 0 h-index: 0机构: Ist Ortoped Rizzoli, Expt Oncol Lab, Bologna, Italy Spanish Natl Canc Res Ctr CNIO, Human Genotyping Unit CeGen, Human Canc Genet Programme, Madrid, SpainKovar, H.论文数: 0 引用数: 0 h-index: 0机构: Med Univ, St Anna Kinderkrebsforsch eV, Childrens Canc Res Inst, Dept Pediat, Vienna, Austria Spanish Natl Canc Res Ctr CNIO, Human Genotyping Unit CeGen, Human Canc Genet Programme, Madrid, SpainDelattre, O.论文数: 0 引用数: 0 h-index: 0机构: Inst Curie, Ctr Rech, INSERM, U830, Paris, France Spanish Natl Canc Res Ctr CNIO, Human Genotyping Unit CeGen, Human Canc Genet Programme, Madrid, SpainGonzalez-Neira, A.论文数: 0 引用数: 0 h-index: 0机构: Spanish Natl Canc Res Ctr CNIO, Human Genotyping Unit CeGen, Human Canc Genet Programme, Madrid, Spain Spanish Natl Canc Res Ctr CNIO, Human Genotyping Unit CeGen, Human Canc Genet Programme, Madrid, Spain
- [4] Identification of rare genetic variants in novel loci associated with Paget's disease of boneHUMAN GENETICS, 2014, 133 (06) : 755 - 768Beauregard, Mariejka论文数: 0 引用数: 0 h-index: 0机构: CHU Quebec, Res Ctr, Quebec City, PQ G1V 4G2, Canada Univ Laval, Dept Med, Div Rheumatol, Quebec City, PQ G1K 7P4, Canada CHU Quebec, Res Ctr, Quebec City, PQ G1V 4G2, CanadaGagnon, Edith论文数: 0 引用数: 0 h-index: 0机构: CHU Quebec, Res Ctr, Quebec City, PQ G1V 4G2, Canada CHU Quebec, Res Ctr, Quebec City, PQ G1V 4G2, CanadaGuay-Belanger, Sabrina论文数: 0 引用数: 0 h-index: 0机构: CHU Quebec, Res Ctr, Quebec City, PQ G1V 4G2, Canada Univ Laval, Dept Med, Div Rheumatol, Quebec City, PQ G1K 7P4, Canada CHU Quebec, Res Ctr, Quebec City, PQ G1V 4G2, CanadaMorissette, Jean论文数: 0 引用数: 0 h-index: 0机构: CHU Quebec, Res Ctr, Quebec City, PQ G1V 4G2, Canada CHU Quebec, Res Ctr, Quebec City, PQ G1V 4G2, CanadaBrown, Jacques P.论文数: 0 引用数: 0 h-index: 0机构: CHU Quebec, Res Ctr, Quebec City, PQ G1V 4G2, Canada Univ Laval, Dept Med, Div Rheumatol, Quebec City, PQ G1K 7P4, Canada CHU Quebec, Dept Rhumatol S763, Quebec City, PQ G1V 4G2, Canada CHU Quebec, Res Ctr, Quebec City, PQ G1V 4G2, CanadaMichou, Laetitia论文数: 0 引用数: 0 h-index: 0机构: CHU Quebec, Res Ctr, Quebec City, PQ G1V 4G2, Canada Univ Laval, Dept Med, Div Rheumatol, Quebec City, PQ G1K 7P4, Canada CHU Quebec, Dept Rhumatol S763, Quebec City, PQ G1V 4G2, Canada CHU Quebec, Res Ctr, Quebec City, PQ G1V 4G2, Canada
- [5] Identification of rare genetic variants in novel loci associated with Paget’s disease of boneHuman Genetics, 2014, 133 : 755 - 768Mariejka Beauregard论文数: 0 引用数: 0 h-index: 0机构: CHU de Québec Research Centre,Division of Rheumatology, Department of MedicineEdith Gagnon论文数: 0 引用数: 0 h-index: 0机构: CHU de Québec Research Centre,Division of Rheumatology, Department of MedicineSabrina Guay-Bélanger论文数: 0 引用数: 0 h-index: 0机构: CHU de Québec Research Centre,Division of Rheumatology, Department of MedicineJean Morissette论文数: 0 引用数: 0 h-index: 0机构: CHU de Québec Research Centre,Division of Rheumatology, Department of MedicineJacques P. Brown论文数: 0 引用数: 0 h-index: 0机构: CHU de Québec Research Centre,Division of Rheumatology, Department of MedicineLaëtitia Michou论文数: 0 引用数: 0 h-index: 0机构: CHU de Québec Research Centre,Division of Rheumatology, Department of Medicine
- [6] Identification of multiple rare variants associated with a diseaseBMC Proceedings, 5 (Suppl 9)Jeesun Jung论文数: 0 引用数: 0 h-index: 0机构: Indiana University School of Medicine,Department of Medical and Molecular GeneticsJessica Dantzer论文数: 0 引用数: 0 h-index: 0机构: Indiana University School of Medicine,Department of Medical and Molecular GeneticsYunlong Liu论文数: 0 引用数: 0 h-index: 0机构: Indiana University School of Medicine,Department of Medical and Molecular Genetics
- [7] COMBINATORIC METHOD FOR IDENTIFICATION OF GENETIC VARIANTS IN RARE DISEASEIRISH JOURNAL OF MEDICAL SCIENCE, 2022, 191 (SUPPL 1) : S13 - S13Kinsella, A.论文数: 0 引用数: 0 h-index: 0机构: Univ Coll Dublin, UCD Sch Med, Dublin 4, Ireland Univ Coll Dublin, UCD Sch Med, Dublin 4, IrelandSegurado, R.论文数: 0 引用数: 0 h-index: 0机构: Univ Coll Dublin, UCD Sch Publ Hlth Physiotherapy & Sports Sci, Dublin 4, Ireland Univ Coll Dublin, UCD CSTAR, Dublin 4, Ireland Univ Coll Dublin, UCD Sch Med, Dublin 4, Ireland
- [8] Rare genetic variants in genes of NO metabolism in lacunar stroke patientsCEREBROVASCULAR DISEASES, 2013, 35 : 39 - 39Loos, C. M. J.论文数: 0 引用数: 0 h-index: 0机构: Maastricht Univ, Med Ctr, Dept Neurol, Maastricht, Netherlands Maastricht Univ, Med Ctr, Cardiovasc Res Inst Maastricht CARIM, Maastricht, Netherlands Maastricht Univ, Med Ctr, Dept Neurol, Maastricht, NetherlandsStaals, J.论文数: 0 引用数: 0 h-index: 0机构: Maastricht Univ, Med Ctr, Dept Neurol, Maastricht, Netherlands Maastricht Univ, Med Ctr, Cardiovasc Res Inst Maastricht CARIM, Maastricht, Netherlands Maastricht Univ, Med Ctr, Dept Neurol, Maastricht, NetherlandsSmeets, H. J. M.论文数: 0 引用数: 0 h-index: 0机构: Maastricht Univ, Med Ctr, Cardiovasc Res Inst Maastricht CARIM, Maastricht, Netherlands Maastricht Univ, Med Ctr, Dept Clin Genom, Maastricht, Netherlands Maastricht Univ, Med Ctr, Dept Neurol, Maastricht, Netherlandsvan Oostenbrugge, R. J.论文数: 0 引用数: 0 h-index: 0机构: Maastricht Univ, Med Ctr, Dept Neurol, Maastricht, Netherlands Maastricht Univ, Med Ctr, Cardiovasc Res Inst Maastricht CARIM, Maastricht, Netherlands Maastricht Univ, Med Ctr, Dept Neurol, Maastricht, Netherlands
- [9] Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke The NHLBI Exome Sequence ProjectJAMA NEUROLOGY, 2015, 72 (07) : 781 - 788Auer, Paul L.论文数: 0 引用数: 0 h-index: 0机构: Univ Wisconsin, Joseph J Zilber Sch Publ Hlth, Milwaukee, WI 53201 USA Fred Hutchinson Canc Res Ctr, Div Publ Hlth Sci, Seattle, WA 98104 USA Univ Wisconsin, Joseph J Zilber Sch Publ Hlth, Milwaukee, WI 53201 USANalls, Mike论文数: 0 引用数: 0 h-index: 0机构: NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USA Univ Wisconsin, Joseph J Zilber Sch Publ Hlth, Milwaukee, WI 53201 USAMeschia, James F.论文数: 0 引用数: 0 h-index: 0机构: Mayo Clin, Dept Neurol, Jacksonville, FL 32224 USA Univ Wisconsin, Joseph J Zilber Sch Publ Hlth, Milwaukee, WI 53201 USAWorrall, Bradford B.论文数: 0 引用数: 0 h-index: 0机构: Univ Virginia, Dept Neurol, Charlottesville, VA 22908 USA Univ Wisconsin, Joseph J Zilber Sch Publ Hlth, Milwaukee, WI 53201 USALongstreth, W. T., Jr.论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Dept Neurol, Seattle, WA 98195 USA Univ Wisconsin, Joseph J Zilber Sch Publ Hlth, Milwaukee, WI 53201 USASeshadri, Sudha论文数: 0 引用数: 0 h-index: 0机构: Boston Univ, Sch Med, Dept Neurol, Boston, MA 02118 USA Univ Wisconsin, Joseph J Zilber Sch Publ Hlth, Milwaukee, WI 53201 USAKooperberg, Charles论文数: 0 引用数: 0 h-index: 0机构: Fred Hutchinson Canc Res Ctr, Div Publ Hlth Sci, Seattle, WA 98104 USA Univ Wisconsin, Joseph J Zilber Sch Publ Hlth, Milwaukee, WI 53201 USABurger, Kathleen M.论文数: 0 引用数: 0 h-index: 0机构: George Washington Univ Hosp, Dept Neurol, Washington, DC USA Univ Wisconsin, Joseph J Zilber Sch Publ Hlth, Milwaukee, WI 53201 USACarlson, Christopher S.论文数: 0 引用数: 0 h-index: 0机构: Fred Hutchinson Canc Res Ctr, Div Publ Hlth Sci, Seattle, WA 98104 USA Univ Wisconsin, Joseph J Zilber Sch Publ Hlth, Milwaukee, WI 53201 USACarty, Cara L.论文数: 0 引用数: 0 h-index: 0机构: Fred Hutchinson Canc Res Ctr, Div Publ Hlth Sci, Seattle, WA 98104 USA Univ Wisconsin, Joseph J Zilber Sch Publ Hlth, Milwaukee, WI 53201 USAChen, Wei-Min论文数: 0 引用数: 0 h-index: 0机构: Univ Virginia, Ctr Publ Hlth Genom, Charlottesville, VA 22908 USA Univ Wisconsin, Joseph J Zilber Sch Publ Hlth, Milwaukee, WI 53201 USACupples, L. Adrienne论文数: 0 引用数: 0 h-index: 0机构: Boston Univ, Sch Publ Hlth, Dept Biostat, Boston, MA USA Univ Wisconsin, Joseph J Zilber Sch Publ Hlth, Milwaukee, WI 53201 USADeStefano, Anita L.论文数: 0 引用数: 0 h-index: 0机构: Boston Univ, Sch Publ Hlth, Dept Biostat, Boston, MA USA Univ Wisconsin, Joseph J Zilber Sch Publ Hlth, Milwaukee, WI 53201 USAFornage, Myriam论文数: 0 引用数: 0 h-index: 0机构: Univ Texas Hlth Sci Ctr Houston, Inst Mol Med, Houston, TX 77030 USA Univ Wisconsin, Joseph J Zilber Sch Publ Hlth, Milwaukee, WI 53201 USAHardy, John论文数: 0 引用数: 0 h-index: 0机构: UCL, Dept Neurosci, Reta Lila Weston Inst, London, England Univ Wisconsin, Joseph J Zilber Sch Publ Hlth, Milwaukee, WI 53201 USAHsu, Li论文数: 0 引用数: 0 h-index: 0机构: Fred Hutchinson Canc Res Ctr, Div Publ Hlth Sci, Seattle, WA 98104 USA Univ Wisconsin, Joseph J Zilber Sch Publ Hlth, Milwaukee, WI 53201 USAJackson, Rebecca D.论文数: 0 引用数: 0 h-index: 0机构: Ohio State Univ, Dept Internal Med, Columbus, OH 43210 USA Univ Wisconsin, Joseph J Zilber Sch Publ Hlth, Milwaukee, WI 53201 USAJarvik, Gail P.论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Dept Med, Seattle, WA USA Univ Wisconsin, Joseph J Zilber Sch Publ Hlth, Milwaukee, WI 53201 USAKim, Daniel S.论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Dept Genome Sci, Seattle, WA 98195 USA Univ Wisconsin, Joseph J Zilber Sch Publ Hlth, Milwaukee, WI 53201 USALakshminarayan, Kamakshi论文数: 0 引用数: 0 h-index: 0机构: Univ Minnesota, Dept Neurol, Minneapolis, MN 55455 USA Univ Wisconsin, Joseph J Zilber Sch Publ Hlth, Milwaukee, WI 53201 USALange, Leslie A.论文数: 0 引用数: 0 h-index: 0机构: Univ N Carolina, Dept Genet, Chapel Hill, NC USA Univ Wisconsin, Joseph J Zilber Sch Publ Hlth, Milwaukee, WI 53201 USA论文数: 引用数: h-index:机构:Quinlan, Aaron R.论文数: 0 引用数: 0 h-index: 0机构: Univ Virginia, Ctr Publ Hlth Genom, Charlottesville, VA 22908 USA Univ Wisconsin, Joseph J Zilber Sch Publ Hlth, Milwaukee, WI 53201 USASingleton, Andrew B.论文数: 0 引用数: 0 h-index: 0机构: NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USA Univ Wisconsin, Joseph J Zilber Sch Publ Hlth, Milwaukee, WI 53201 USAThornton, Timothy A.论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Dept Biostat, Seattle, WA 98195 USA Univ Wisconsin, Joseph J Zilber Sch Publ Hlth, Milwaukee, WI 53201 USANickerson, Deborah A.论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Dept Genome Sci, Seattle, WA 98195 USA Univ Wisconsin, Joseph J Zilber Sch Publ Hlth, Milwaukee, WI 53201 USAPeters, Ulrike论文数: 0 引用数: 0 h-index: 0机构: Fred Hutchinson Canc Res Ctr, Div Publ Hlth Sci, Seattle, WA 98104 USA Univ Wisconsin, Joseph J Zilber Sch Publ Hlth, Milwaukee, WI 53201 USARich, Stephen S.论文数: 0 引用数: 0 h-index: 0机构: Univ Virginia, Ctr Publ Hlth Genom, Charlottesville, VA 22908 USA Univ Wisconsin, Joseph J Zilber Sch Publ Hlth, Milwaukee, WI 53201 USA
- [10] RARE GENETIC VARIANTS ARE ASSOCIATED WITH AUTOIMMUNE HEPATITIS RISKHEPATOLOGY, 2022, 76 : S1515 - S1516Lammert, Craig论文数: 0 引用数: 0 h-index: 0机构: Indiana Univ Sch Med, Gastroenterol & Hepatol, Indianapolis, IN USA Indiana Univ Sch Med, Gastroenterol & Hepatol, Indianapolis, IN USA论文数: 引用数: h-index:机构:Schwantes-An, Tae-Hwi论文数: 0 引用数: 0 h-index: 0机构: Indiana Univ Sch Med, Med & Mol Genet, Indianapolis, IN USA Indiana Univ Sch Med, Gastroenterol & Hepatol, Indianapolis, IN USA