共 50 条
- [1] Whole genome and exome sequencing of monozygotic twins discordant for Crohn’s diseaseBMC Genomics, 15Britt-Sabina PetersenMartina E SpehlmannAndreas RaedlerBjörn StadeIngo ThomsenRaquel RabionetPhilip RosenstielStefan SchreiberAndre Franke
- [2] Is Whole Exome Sequencing Clinically Practical in the Management of Pediatric Crohn's Disease?GUT AND LIVER, 2015, 9 (06) : 767 - 775Oh, Seak HeeBaek, JiwonKim, Kyung MoLee, Eun-JuJung, YusunLee, Yeoun JooJin, Hyun-SeungYe, Byong DukYang, Suk-KyunLee, Jong-KeukSeo, Eul-JuLim, Hyun TaekLee, InchulSong, Kyuyoung
- [3] Whole genome and exome sequencing of monozygotic twins discordant for Crohn's diseaseBMC GENOMICS, 2014, 15Petersen, Britt-SabinaSpehlmann, Martina E.Raedler, AndreasStade, BjoernThomsen, IngoRabionet, RaquelRosenstiel, PhilipSchreiber, StefanFranke, Andre
- [4] Rare pathogenic variants in whole exome sequencing data of Bulgarian Alzheimer's disease patientsEUROPEAN JOURNAL OF HUMAN GENETICS, 2023, 31 : 197 - 198Karachanak-Yankova, SenaNikolova, DragomiraMihaylova, MartaSerbezov, DimitarBalabanski, LubomirDamyanova, VeraAntonova, OlgaStaneva, RadaGanev, MihailSpasova, VictoriaRukova, BlagaNesheva, DesislavaJosifovska, SlavicaBelejanska, DianaPetrova, MariyaMehrabian, ShimaTraykov, LatchezarHadjidekova, SavinaToncheva, Draga
- [5] Genetic variants associated with Crohn's diseaseAPPLICATION OF CLINICAL GENETICS, 2013, 6 : 25 - 32Michail, SoniaBultron, GilbertoDePaolo, R. William
- [6] WHOLE EXOME SEQUENCING OF A MULTIPLEX CROHN'S DISEASE FAMILY IDENTIFIES RARE ALTERATIONS IN PYGB ANDXRN2 AS POTENTIALLY HIGH IMPACT RISK VARIANTS OF DISEASEGASTROENTEROLOGY, 2023, 164 (04) : S50 - S51Chen, Lea AnnKim, MinsukLi, DalinAita, RohitCataldo, SusanRadin, ArielleBaylor, JessicaDeng, LilyHahn, BrettWong, KevinTin, KevinMengesha, EmebetMcGovern, Dermot
- [7] WHOLE EXOME SEQUENCING OF A MULTIPLEX CROHN'S DISEASE FAMILY IDENTIFIES RARE ALTERATIONS IN PYGB AND XRN2 AS POTENTIALLY HIGH IMPACT RISK VARIANTS OF DISEASEGASTROENTEROLOGY, 2023, 164 (06) : S437 - S437Chen, Lea AnnKim, MinsukLi, DalinAita, RohitCataldo, SusanRadin, ArielleBaylor, JessicaDeng, LilyHahn, BrettWong, KevinTin, KevinMengesha, EmebetMcgovern, Dermot P. B.
- [8] WHOLE EXOME SEQUENCING OF A MULTIPLEX CROHN'S DISEASE FAMILY IDENTIFIES RARE ALTERATIONS IN PYGB AND XRN2 AS POTENTIALLY HIGH IMPACT RISK VARIANTS OF DISEASEINFLAMMATORY BOWEL DISEASES, 2023, 29 : S40 - S40Chen, Lea AnnKim, MinsukLi, DalinAita, RohitCataldo, SusanRadin, ArielleBaylor, JessicaDeng, LilyHahn, BrettWong, KevinTin, KevinMengesha, EmebetMcGovern, Dermot
- [9] VULVAR CROHN'S: A RARE PRESENTATION OF CROHN'S DISEASEJOURNAL OF SEXUAL MEDICINE, 2018, 15 (06) : S119 - S120Cigna, S.Mitchell, L.Goldstein, A.
- [10] Large-scale sequencing identifies multiple genes and rare variants associated with Crohn’s disease susceptibilityNature Genetics, 2022, 54 : 1275 - 1283Aleksejs SazonovsChristine R. StevensGuhan R. VenkataramanKai YuanBrandon AvilaMaria T. AbreuTariq AhmadMatthieu AllezAshwin N. AnanthakrishnanGil AtzmonAris BarasJeffrey C. BarrettNir BarzilaiLaurent BeaugerieAshley BeechamCharles N. BernsteinAlain BittonBernd BokemeyerAndrew ChanDaniel ChungIsabelle CleynenJacques CosnesDavid J. CutlerAllan DalyOriana M. DamasLisa W. DattaNoor DawanyMarcella DevotoSheila DodgeEva EllinghausLaura FachalMartti FarkkilaWilliam FaubionManuel FerreiraDenis FranchimontStacey B. GabrielTian GeMichel GeorgesKyle GettlerMamta GiriBenjamin GlaserSiegfried GoergPhilippe GoyetteDaniel GrahamEija HämäläinenTalin HarituniansGraham A. HeapMikko HiltunenMarc HoeppnerJulie E. Horowitz