37 Publications (Page 1 of 2)
2020
Chromosomal instability in untreated primary prostate cancer as an indicator of metastatic potential.
Miller, Eric TYou, SungyongCadaneanu, Radu MKim, MinhyungYoon, JunheeLiu, Sandy TLi, XinminKwan, LornaHodge, JennelleQuist, Michael JGrasso, Catherine SLewis, Michael SKnudsen, Beatrice SFreeman, Michael R and Garraway, Isla P
BMC cancer, vol. 20, (no. 1), pp. 398, May 7, 2020. | Journal Article
 
Non-fusion mutations in endometrial stromal sarcomas: what is the potential impact on tumourigenesis through cell cycle dysregulation?
Patel, Snehal BMcCormack, Colin and Hodge, Jennelle C
Journal of clinical pathology, pp. jclinpath-2020-206432, 2020-May-08. | Journal Article
2019
Correction: A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delay
BE, MuchaMucha, B.E.Mucha, Bettina ES, BankaBanka, SiddharthBanka, S.Ajeawung, N.F.NF, AjeawungAjeawung, Norbert FonyaMolidperee, SirinartS, MolidpereeMolidperee, S.Chen, Gary GChen, G.G.GG, ChenKoenig, M.K.MK, KoenigKoenig, Mary KayAdejumo, R.B.Adejumo, Rhamat BRB, AdejumoM, TillTill, MarianneTill, M.M, HarbordHarbord, MichaelHarbord, M.Perrier, R.R, PerrierPerrier, ReneeLemyre, E.Lemyre, EmmanuelleE, LemyreRM, BoucherBoucher, R.-M.Boucher, Renee-MyriamBG, SkotkoSkotko, B.G.Skotko, Brian GWaxler, Jessica LWaxler, J.L.PM, CampeauThomas, Mary AnnThomas, M.A.Hodge, Jennelle CHodge, J.C.Gecz, J.Gecz, JozefNicholl, JillianNicholl, J.McGregor, LesleyMcGregor, L.Linden, TobiasLinden, T.Sisodiya, Sanjay MSisodiya, S.M.Sanlaville, D.Sanlaville, DamienCheung, Sau WCheung, S.W.Ernst, CarlErnst, C.Campeau, P.M. and Campeau, Philippe M
Genetics in medicine : official journal of the American College of Medical Genetics, vol. 21, (no. 9), pp. 2160, 2019-Sep. | Journal Article
2018
5. Progress and future of the compendium of Cancer Genome Aberrations (CCGA)
Hodge, Jennelle CCooley, LindaChen, HuiYang, FeiPitel, BethSathanoori, MaliniDavis, BrianCorboy, GregGriffith, ObiBaughn, LindaNewman, Scott and Wolff, Daynna J
Cancer Genetics, vol. 226-227, pp. 38, October 2018. | Journal Article
 
A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delay.
Mucha, Bettina EMucha, Bettina EMucha, B.E.BE, MuchaBanka, S.S, BankaBanka, SiddhartBanka, SiddharthAjeawung, N.F.Ajeawung, Norbert FonyaNF, AjeawungAjeawung, Norbert FonyaMolidperee, SirinartMolidperee, S.Molidperee, SirinartS, MolidpereeChen, Gary GChen, G.G.Chen, Gary GGG, ChenKoenig, Mary KayKoenig, Mary KayKoenig, M.K.MK, KoenigAdejumo, R.B.Adejumo, Rhamat BRB, AdejumoAdejumo, Rhamat BM, TillTill, MarianneTill, MarianneTill, M.Harbord, MichaelM, HarbordHarbord, M.Harbord, MichaelPerrier, ReneeR, PerrierPerrier, ReneePerrier, R.Lemyre, EmmanuelleLemyre, E.E, LemyreLemyre, EmmanuelleBoucher, Renee-MyriamRM, BoucherBoucher, Renee-MyriamBoucher, R.-M.Skotko, Brian GSkotko, B.G.Skotko, Brian GBG, SkotkoWaxler, Jessica LWaxler, Jessica LPM, CampeauWaxler, J.L.Thomas, Mary AnnThomas, Mary AnnThomas, M.A.Hodge, Jennelle CHodge, Jennelle CHodge, J.C.Gecz, J.Gecz, JozefGecz, JozefNicholl, JillianNicholl, J.Nicholl, JillianMcGregor, L.McGregor, LesleyMcGregor, LesleyLinden, T.Linden, TobiasLinden, TobiasSisodiya, S.M.Sisodiya, Sanjay MSisodiya, Sanjay MSanlaville, DamienSanlaville, DamienSanlaville, D.Cheung, Sau WCheung, S.W.Cheung, Sau WErnst, CarlErnst, CarlErnst, C.Campeau, Philippe MCampeau, Philippe M and Campeau, P.M.
Genetics in medicine : official journal of the American College of Medical Genetics, September 24, 2018. | Journal Article
 
Assessing copy number aberrations and copy neutral loss of heterozygosity across the genome as best practice: An evidence based review of clinical utility from the cancer genomics consortium (CGC) working group for myelodysplastic syndrome, myelodysplastic/myeloproliferative and myeloproliferative neoplasms.
Kanagal-Shamanna, RashmiHodge, Jennelle CTucker, TracyShetty, ShashiYenamandra, AshwiniDixon-McIver, AmandaBryke, ChristineHuxley, EmmaLennon, Patrick ARaca, GordanaXu, XinjieJeffries, SallyQuintero-Rivera, FabiolaGreipp, Patricia TSlovak, Marilyn LIqbal, M Anwar and Fang, Min
Cancer genetics, October 10, 2018. | Journal Article
 
Assessing copy number abnormalities and copy-neutral loss-of-heterozygosity across the genome as best practice in diagnostic evaluation of acute myeloid leukemia: An evidence-based review from the cancer genomics consortium (CGC) myeloid neoplasms working group.
Xu, XinjieBryke, ChristineSukhanova, MadinaHuxley, EmmaDash, D PDixon-Mciver, AmandaFang, MinGriepp, Patricia THodge, Jennelle CIqbal, AnwarJeffries, SallyKanagal-Shamanna, RashmiQuintero-Rivera, FabiolaShetty, ShashiSlovak, Marilyn LYenamandra, AshwiniLennon, Patrick A and Raca, Gordana
Cancer genetics, vol. 228-229, pp. 218-235, December 2018. | Journal Article
 
Molecular and pathologic characterization of AML with double Inv(3)(q21q26.2).
Hodge, Jennelle CBosler, DavidRubinstein, LaurenSadri, Navid and Shetty, Shashirekha
Cancer genetics, November 16, 2018. | Journal Article
2017
Genomic Copy Number Aberrations and Copy Neutral Loss of Heterozygosity Evaluation in Myeloid Neoplasms: Evidence-Based Recommendations for Clinical Genetic Testing From the Myeloid Malignancies Working Group of the Cancer Genomics Consortium
Hodge, JennelleHodge, JennelleKanagal-Shamanna, RashmiKanagal Shamanna, RashmiXu, XinjieXu, XinjieBryke, ChristineBryke, ChristineDash, D.PDash, D.PDixon-Mciver, AmandaDixon-Mciver, AmandaGreipp, PattyGreipp, PattyHuxley, EmmaHuxley, EmmaJeffries, SallyJeffries, SallyLennon, PatrickLennon, PatrickQuintero-Rivera, FabiolaQuintero-Rivera, FabiolaShetty, ShashiShetty, ShashiSukhanova, MadinaSukhanova, MadinaTucker, TracyTucker, TracyYenamandra, AshwiniYenamandra, AshwiniSlovak, MarilynSlovak, MarilynIqbal, AnwarIqbal, AnwarFang, MinFang, MinRaca, Gordana and Raca, Gordana
Cancer Genetics, vol. 214, pp. 37, 2017. | Journal Article
 
The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies
Redin, ClaireRedin, ClaireRedin, C.Redin, Claire......Brand, HarrisonBrand, HarrisonBrand, H.Brand, HarrisonCollins, R.L.Collins, RyanCollins, RyanCollins, Ryan LKammin, TammyKammin, TammyKammin, TammyKammin, T.Mitchell, ElyseMitchell, E.Mitchell, ElyseMitchell, ElyseHodge, JennelleHodge, J.C.Hodge, Jennelle CHodge, JennelleHanscom, C.Hanscom, CarrieHanscom, CarrieHanscom, CarriePillalamarri, VamseePillalamarri, VamseePillalamarri, V.Pillalamarri, VamseeSeabra, C.M.Seabra, CatarinaSeabra, CatarinaSeabra, Catarina MAbbott, Mary-AliceAbbott, Mary-AliceAbbott, M.-A.Abbott, MaryAbdul-Rahman, O.A.Nieuwint, AggieAbdul-Rahman, OmarAbdul-Rahman, Omar AAberg, ErikaAberg, E.Aberg, ErikaOrdulu, ZehraParkash, SandhyaAdley, RhettAdley, RhettAdley, R.Alcaraz-Estrada, S.L.Alcaraz-Estrada, Sofia LPauker, SusanAlcaraz-Estrada, SofiaPereira, ShahrinAlkuraya, FowzanAlkuraya, F.S.Alkuraya, Fowzan SAn, YuAn, Y.An, YuPerrin, DanielleAnderson, MaryAnderson, Mary-AnnePhelan, KatyAnderson, M.-A.Antolik, CarolinePiña Aguilar, RaulAntolik, C.Antolik, CarolineAnyane-Yeboa, KwameAnyane-Yeboa, KwamePoddighe, PinoAnyane-Yeboa, K.Atkin, J.F.Pregno, GiuliaAtkin, Joan FAtkin, JoanAbdul-Rahman, OmarBartell, TinaBartell, T.Bartell, TinaBernstein, Jonathan ABernstein, J.A.Raskin, SalmoBernstein, JonathanReis, LindaBeyer, E.Beyer, ElizabethBeyer, ElizabethBlumenthal, IanBlumenthal, I.Blumenthal, IanRhead, WilliamRita, DebraBongers, Ernie M. H. FBongers, E.M.H.F.Bongers, ErnieBrilstra, Eva HBrilstra, EvaRenkens, IvoBrilstra, E.H.Roelens, FilipBrown, Chester WBrown, ChesterBrown, C.W.Brüggenwirth, Hennie TBrüggenwirth, H.T.Brüggenwirth, HennieRuliera, JaylaCallewaert, BertCallewaert, B.Rump, PatrickCallewaert, BertChiang, ColbySchilit, SamanthaChiang, C.Chiang, ColbyCorning, KenCorning, K.Shaheen, RanadCorning, KenCox, HelenCox, HelenAberg, ErikaCox, H.Cuppen, EdwinCuppen, E.Sparkes, RebeccaCuppen, EdwinSpiegel, EricaCurrall, B.B.Currall, BenjaminCurrall, Benjamin BStevens, BlairCushing, T.Cushing, TomCushing, TomStone, MatthewDavid, D.David, DezsoDavid, DezsoTagoe, JuliaDeardorff, M.A.Deardorff, MatthewDeardorff, Matthew ADheedene, AnneliesDheedene, AnneliesDheedene, A.Thakuria, JosephD’Hooghe, M.D Hooghe, Marcvan Bon, BregjeD'Hooghe, MarcDe Vries, B.B.A.van de Kamp, JiddekeVries, Bert B. ADe Vries, BertEarl, Dawnvan Der Burgt, InekeEarl, Dawn LEarl, D.L.Ferguson, Heather LFerguson, HeatherFerguson, H.L.van Essen, TonAdley, RhettFisher, HeatherFisher, H.Fisher, HeatherFitzPatrick, D.R.FitzPatrick, Davidvan Ravenswaaij-Arts, ConnyFitzpatrick, David RGerrol, PamelaGerrol, P.van Roosmalen, MarkusGerrol, PamelaVergult, SarahGiachino, DanielaGiachino, D.Giachino, DanielaGlessner, Joseph TVolker-Touw, CatharinaGlessner, J.T.Glessner, JosephWarburton, DorothyGliem, T.Gliem, TroyGliem, TroyWaterman, MatthewGrady, MargoGrady, M.Grady, MargoGraham, B.H.Wiley, SusanGraham, Brett HGraham, BrettWilson, AnnaGriffis, C.Griffis, CristinGriffis, CristinGripp, K.W.Zori, RobertoGripp, KarenGripp, Karen WGropman, A.L.Gropman, AneaLevy, BrynnGropman, Andrea LHanson-Kahn, AneaHanson-Kahn, AndreaAlcaraz-Estrada, SofiaHanson-Kahn, A.Harris, D.J.Harris, David JBrunner, HanHarris, DavidHayden, M.A.Hayden, Mark AHayden, Markde Leeuw, NicoleHill, RosamundKloosterman, WigardHill, R.Hill, RosamundHochstenbach, R.Hochstenbach, RonHochstenbach, RonThorland, ErikHoffman, JodiMorton, CynthiaHoffman, Jodi DHoffman, J.D.Hopkin, Robert JHopkin, R.J.Hopkin, RobertGusella, JamesTalkowski, MichaelHubshman, MonikaHubshman, Monika WHubshman, M.W.Innes, A.M.Innes, A. MicheilAlkuraya, FowzanInnes, A.An, YuIrons, M.Irons, MiraIrons, MiraAnderson, Mary-AnneIrving, MelitaIrving, MelitaIrving, M.Jacobsen, JessieAntolik, CarolineJacobsen, J.C.Jacobsen, Jessie CJanssens, SanaAnyane-Yeboa, KwameJanssens, S.Janssens, SandraJewett, TamisonAtkin, JoanJewett, TamisonJewett, T.Johnson, JohnJohnson, John PJohnson, J.P.Bartell, TinaJongmans, Marjolijn CJongmans, MarjolijnBernstein, JonathanJongmans, M.C.Beyer, ElizabethKahler, StephenKahler, Stephen GKahler, S.G.Koolen, D.A.Koolen, DavidKoolen, David ABlumenthal, IanKorzelius, J.Korzelius, JeromeKorzelius, JeromeBrilstra, EvaKroisel, PeterKroisel, P.M.Brown, ChesterKroisel, Peter MLacassie, YvesLacassie, YvesLacassie, Y.Brüggenwirth, HennieCallewaert, BertLawless, WilliamLawless, W.Lawless, WilliamLemyre, EmmanuelleLemyre, EmmanuelleLemyre, E.Chiang, ColbyLeppig, KathleenLeppig, K.Leppig, KathleenCorning, KenLevin, Alex VLevin, AlexCox, HelenLevin, A.V.Li, HaiboLi, HaiboLi, H.Cuppen, EdwinLi, HongLi, H.Li, HongCurrall, BenjaminLiao, E.C.Cushing, TomLiao, Eric CLiao, EricLim, CynthiaDavid, DezsoLim, CynthiaLim, C.Lose, Edward JLose, E.J.Lose, EdwardDeardorff, MatthewLucente, DianeLucente, DianeLucente, D.Dheedene, AnneliesMacEra, MichaelMacEra, M.J.D'Hooghe, MarcMacera, Michael JManavalan, P.Manavalan, PoornimaManavalan, PoornimaEarl, DawnManile, GiorgiaMandrile, G.Mandrile, GiorgiaFerguson, HeatherMarcelis, C.L.Marcelis, Carlo LFisher, HeatherMarcelis, CarloMargolin, LaurenFitzPatrick, DavidMargolin, L.Margolin, LaurenMason, TamaraMason, T.Gerrol, PamelaMason, TamaraGiachino, DanielaMasser-Frye, DianeMasser-Frye, D.Masser-Frye, DianeGlessner, JosephMcclellan, Michael WMcClellan, MichaelMcClellan, M.W.Mendoza, Cinthya J. ZepedaGliem, TroyZepeda Mendoza, CinthyaZepeda Mendoza, C.J.Menten, B.Grady, MargoMenten, BjörnMenten, BjörnGraham, BrettMiddelkamp, S.Middelkamp, SjorsMiddelkamp, SjorsMikami, Liya RMikami, LiyaGriffis, CristinMikami, L.R.Moe, EmilyMoe, E.Moe, EmilyGripp, KarenMohammed, S.Mohammed, ShehlaGropman, AndreaMohammed, ShehlaMononen, TarjaMononen, T.Mononen, TarjaHanson-Kahn, AndreaHarris, DavidMortenson, Megan EMortenson, MeganMortenson, M.E.Moya, G.Hayden, MarkHill, RosamundNieuwint, A.W.Ordulu, Z.Hochstenbach, RonHoffman, JodiParkash, S.Pauker, S.P.Hopkin, RobertHubshman, MonikaPereira, S.Innes, APerrin, D.Irons, MiraPhelan, K.Piña Aguilar, R.E.Irving, MelitaJacobsen, JessiePoddighe, P.J.Janssens, SandraPregno, G.Raskin, S.Jewett, TamisonJohnson, JohnReis, L.Rhead, W.Jongmans, MarjolijnKahler, StephenRita, D.Renkens, I.Koolen, DavidKorzelius, JeromeRoelens, F.Ruliera, J.Kroisel, PeterLacassie, YvesRump, P.Schilit, S.L.P.Lawless, WilliamShaheen, R.Lemyre, EmmanuelleLeppig, KathleenSparkes, R.Levin, AlexSpiegel, E.Li, HaiboStevens, B.Stone, M.R.Li, HongLiao, EricTagoe, J.Thakuria, J.V.Lim, CynthiaVan Bon, B.W.Lose, EdwardVan De Kamp, J.Lucente, DianeMacera, MichaelVan Der Burgt, I.Van Essen, T.Manavalan, PoornimaVan Ravenswaaij-Arts, C.M.Mandrile, GiorgiaVan Roosmalen, M.J.Marcelis, CarloVergult, S.Margolin, LaurenMason, TamaraVolker-Touw, C.M.L.Masser-Frye, DianeWarburton, D.P.McClellan, MichaelWaterman, M.J.Wiley, S.Zepeda Mendoza, CinthyaMenten, BjörnWilson, A.Middelkamp, SjorsYerena-De Vega, M.D.L.C.A.Zori, R.T.Mikami, LiyaLevy, B.Moe, EmilyBrunner, H.G.Mohammed, ShehlaMononen, TarjaDe Leeuw, N.Mortenson, MeganKloosterman, W.P.Moya, GracielaThorland, E.C.Morton, C.C.Gusella, J.F. and Talkowski, M.E.
pp. 45, 2017-01-01. | Journal Article
2016
Molecular Cytogenetic Analysis of JAZF1 , PHF1 , and YWHAE in Endometrial Stromal Tumors
Hodge, JennelleBedroske, PatrickPearce, Kathryn and Sukov, William
Journal of Molecular Diagnostics, The, vol. 18, (no. 4), pp. 526, 2016. | Journal Article
2015
Analysis of MDM2 Amplification in 43 Endometrial Stromal Tumors: A Potential Diagnostic Pitfall
Schoolmeester, JSchoolmeester, J KennethSciallis, AndrewSciallis, Andrew PGreipp, PatriciaGreipp, Patricia THodge, JennelleHodge, Jennelle CDal Cin, PaolaDal Cin, PaolaKeeney, Gary LKeeney, GaryNucci, Marisa R and Nucci, Marisa
International Journal of Gynecological Pathology, vol. 34, (no. 6), pp. 583, 2015-November. | Journal Article
 
Recurrent duplications of 17q12 associated with variable phenotypes
Mitchell, ElyseMitchell, ElyseDouglas, AndrewDouglas, AndrewKjaegaard, SusanneKjaegaard, SusanneCallewaert, BertCallewaert, BertVanlander, ArnaudVanlander, ArnaudJanssens, SandraJanssens, SandraYuen, Amy LawsonYuen, Amy LawsonSkinner, CindySkinner, CindyFailla, PinellaFailla, PinellaAlberti, AntoninoAlberti, AntoninoAvola, EmanuelaAvola, EmanuelaFichera, MarcoFichera, MarcoKibaek, MariaKibaek, MariaDigilio, Maria CDigilio, Maria CHannibal, Mark CHannibal, Mark Cden Hollander, Nicolette Sden Hollander, Nicolette SBizzarri, VeronicaBizzarri, VeronicaRenieri, AlessandraRenieri, AlessandraMencarelli, Maria AntoniettaMencarelli, Maria AntoniettaFitzgerald, TomasFitzgerald, TomasPiazzolla, SerenaPiazzolla, Serenavan Oudenhove, Elkevan Oudenhove, ElkeRomano, CorradoRomano, CorradoSchwartz, CharlesSchwartz, CharlesEichler, Evan EEichler, Evan ESlavotinek, AnneSlavotinek, AnneEscobar, LuisEscobar, LuisRajan, DianaRajan, DianaCrolla, JohnCrolla, JohnCarter, NigelCarter, NigelHodge, Jennelle CHodge, Jennelle CMefford, Heather C and Mefford, Heather C
American Journal of Medical Genetics Part A, vol. 167, (no. 12), pp. 3045, December 2015. | Journal Article
2014
Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes
Lionel, Anath CLionel, Anath CLionel, Anath C.Tammimies, KristiinaTammimies, KristiinaTammimies, KristiinaVaags, Andrea KVaags, Andrea K.Vaags, Andrea KRosenfeld, Jill ARosenfeld, Jill ARosenfeld, Jill A.Ahn, Joo WookAhn, Joo WMerico, DanieleMerico, DanieleMerico, DanieleNoor, AbdulNoor, AbdulNoor, AbdulRunke, Cassandra KRunke, Cassandra KRunke, Cassandra K.Pillalamarri, Vamsee KPillalamarri, Vamsee KPillalamarri, Vamsee K.Carter, Melissa TCarter, Melissa T.Carter, Melissa TGazzellone, Matthew JGazzellone, Matthew JGazzellone, Matthew J.Thiruvahindrapuram, BhoomaThiruvahindrapuram, BhoomaThiruvahindrapuram, BhoomaFagerberg, ChristinaFagerberg, ChristinaFagerberg, ChristinaLaulund, Lone W.Laulund, Lone WLaulund, Lone WPellecchia, GiovannaPellecchia, GiovannaPellecchia, GiovannaLamoureux, SylviaLamoureux, SylviaLamoureux, SylviaDeshpande, CharuDeshpande, CharuDeshpande, CharuClayton-Smith, JillClayton-Smith, JillClayton-Smith, JillWhite, Ann C.White, Ann CWhite, Ann CLeather, SusanLeather, SusanLeather, SusanTrounce, JohnTrounce, JohnTrounce, JohnMelanie Bedford, HMelanie Bedford, HBedford, H. MelanieHatchwell, EliHatchwell, EliHatchwell, EliEis, Peggy SEis, Peggy S.Eis, Peggy SYuen, Ryan KYuen, Ryan K. C.Yuen, Ryan K.CWalker, SusanWalker, SusanWalker, SusanUddin, MohammedUddin, MohammedUddin, MohammedGeraghty, Michael TGeraghty, Michael T.Geraghty, Michael TNikkel, Sarah M.Nikkel, Sarah MNikkel, Sarah MTomiak, Eva M.Tomiak, Eva MTomiak, Eva MFernandez, Bridget A.Fernandez, BridgetFernandez, Bridget ASoreni, NoamSoreni, NoamSoreni, NoamCrosbie, JenniferCrosbie, JenniferCrosbie, JenniferArnold, Paul D.Arnold, Paul DArnold, Paul DSchachar, Russell J.Schachar, Russell JSchachar, Russell JRoberts, WendyRoberts, WendyRoberts, WendyPaterson, Andrew D.Paterson, Andrew DPaterson, Andrew DSo, JoyceSo, JoyceSo, JoyceSzatmari, PeterSzatmari, PeterSzatmari, PeterChrysler, ChristinaChrysler, ChristinaChrysler, ChristinaWoodbury-Smith, MarcWoodbury-Smith, MarcWoodbury-Smith, MarcLowry, R. BrianBrian Lowry, RBrian Lowry, RZwaigenbaum, LonnieZwaigenbaum, LonnieZwaigenbaum, LonnieMandyam, DivyaMandyam, DivyaMandyam, DivyaWei, JohnWei, JohnWei, JohnMacDonald, Jeffrey RMacdonald, Jeffrey RMacDonald, Jeffrey R.Howe, Jennifer L.Howe, Jennifer LHowe, Jennifer LNalpathamkalam, ThomasNalpathamkalam, ThomasNalpathamkalam, ThomasWang, ZhuozhiWang, ZhuozhiWang, ZhuozhiTolson, DanielTolson, DanielTolson, DanielCobb, David SCobb, David SCobb, David S.Wilks, Timothy M.Wilks, Timothy MWilks, Timothy MSorensen, Mark J.Sorensen, Mark JSorensen, Mark JBader, Patricia IBader, Patricia I.Bader, Patricia IAn, YuAn, YuAn, YuWu, Bai-LinWu, Bai-LinWu, Bai-LinMusumeci, Sebastiano AMusumeci, Sebastiano AntoninoRomano, CorradoRomano, CorradoRomano, CorradoPostorivo, DianaPostorivo, DianaPostorivo, DianaNardone, Anna MNardone, Anna M.Nardone, Anna MDella Monica, MatteoMonica, Matteo DellaMonica, Matteo DScarano, GioacchinoScarano, GioacchinoScarano, GioacchinoZoccante, LeonardoZoccante, LeonardoZoccante, LeonardoNovara, FrancescaNovara, FrancescaNovara, FrancescaZuffardi, OrsettaZuffardi, OrsettaZuffardi, OrsettaCiccone, RobertoCiccone, RobertoCiccone, RobertoAntona, VincenzoAntona, VincenzoAntona, VincenzoCarella, MassimoCarella, MassimoCarella, MassimoZelante, LeopoldoZelante, LeopoldoZelante, LeopoldoCavalli, PietroCavalli, PietroCavalli, PietroPoggiani, CarloPoggiani, CarloPoggiani, CarloCavallari, UgoCavallari, UgoCavallari, UgoArgiropoulos, BobArgiropoulos, BobArgiropoulos, BobChernos, JudyChernos, JudyChernos, JudyBrasch-Andersen, CharlotteBrasch-Andersen, CharlotteBrasch-Andersen, CharlotteSpeevak, MarshaSpeevak, MarshaSpeevak, MarshaFichera, MarcoFichera, MarcoFichera, MarcoOgilvie, Caroline MackieOgilvie, Caroline MShen, YipingShen, YipingShen, YipingHodge, Jennelle C.Hodge, Jennelle CHodge, Jennelle CTalkowski, Michael ETalkowski, Michael E.Talkowski, Michael EStavropoulos, Dimitri JStavropoulos, Dimitri J.Stavropoulos, Dimitri JMarshall, Christian R.Marshall, Christian RMarshall, Christian RScherer, Stephen WScherer, Stephen W. and Scherer, Stephen W
Human Molecular Genetics, vol. 23, (no. 10), pp. 2768, 20140515. | Journal Article
 
High-grade Endometrial Stromal Sarcomas: A Clinicopathologic Study of a Group of Tumors With Heterogenous Morphologic and Genetic Features
Sciallis, Andrew PSciallis, AndrewBedroske, Patrick PBedroske, PatrickSchoolmeester, John KSchoolmeester, JohnSukov, William RSukov, WilliamKeeney, Gary LKeeney, GaryHodge, Jennelle CHodge, JennelleBell, Debra A and Bell, Debra
The American Journal of Surgical Pathology, vol. 38, (no. 9), pp. 1172, 2014-September. | Journal Article
 
Molecular cytogenetic analysis for TFE3 rearrangement in Xp11.2 renal cell carcinoma and alveolar soft part sarcoma: validation and clinical experience with 75 cases
Hodge, Jennelle CPearce, Kathryn EWang, XiaokeWiktor, Anne EOliveira, Andre M and Greipp, Patricia T
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, vol. 27, (no. 1), pp. 127, 2014-Jan. | Journal Article
 
Recurrent 8q13.2-13.3 microdeletions associated with Branchio-oto-renal syndrome are mediated by human endogenous retroviral (HERV) sequence blocks
Chen, XiaoliWang, JunMitchell, ElyseGuo, JinWang, LiwenZhang, YuHodge, Jennelle C and Shen, Yiping
BMC medical genetics, vol. 15, (no. 1), pp. 90, 2014-Aug-19. | Journal Article
2013
Deletions in 16q24.2 are associated with autism spectrum disorder, intellectual disability and congenital renal malformation
Handrigan, Gregory RHandrigan, Gregory RyanChitayat, DavidChitayat, David ALionel, Anath CLionel, Anath CPinsk, MauryPinsk, MauryVaags, Andrea KVaags, Andrea KMarshall, Christian RMarshall, Christian RDyack, SarahDyack, SarahEscobar, Luis FEscobar, Luis FFernandez, Bridget AFernandez, BridgetStegman, Joseph CStegman, Joseph CRosenfeld, Jill ARosenfeld, Jill AShaffer, Lisa GShaffer, Lisa GGoodenberger, McKinseyGoodenberger, McKinseyHodge, Jennelle CHodge, Jennelle CCain, Jason ECain, Jason EBabul-Hirji, RiyanaBabul-Hirji, RiyanaStavropoulos, Dimitri JStavropoulos, Dimitri JYiu, VernaYiu, VernaScherer, Stephen WScherer, Stephen WRosenblum, Norman D and Rosenblum, Norman D
Journal of Medical Genetics, vol. 50, (no. 3), pp. 173, 20130300. | Journal Article
 
Distinct ALK-rearranged and VCL-negative papillary renal cell carcinoma variant in two adults without sickle cell trait
Hodge, Jennelle CPearce, Kathryn E and Sukov, William R
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, vol. 26, (no. 4), pp. 605, 2013-Apr. | Journal Article
 
JAZF1 Rearrangement in a Mesenchymal Tumor of Nonendometrial Stromal Origin: Report of an Unusual Ossifying Sarcoma of the Heart Demonstrating JAZF1/PHF1 Fusion
Schoolmeester, J KSchoolmeester, JSukov, WilliamSukov, William RMaleszewski, Joseph JMaleszewski, JosephBedroske, Patrick PBedroske, PatrickFolpe, Andrew LFolpe, AndrewHodge, Jennelle and Hodge, Jennelle C
The American Journal of Surgical Pathology, vol. 37, (no. 6), pp. 942, 2013-June. | Journal Article
 
Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures
Lionel, Anath CLionel, Anath CLionel, Anath CVaags, Andrea KVaags, Andrea KVaags, Andrea KSato, DaisukeSato, DaisukeSato, DaisukeGazzellone, Matthew JGazzellone, Matthew JGazzellone, Matthew JMitchell, Elyse BMitchell, Elyse BMitchell, Elyse BChen, Hong YangChen, Hong YChen, Hong YangCostain, GregoryCostain, GregoryCostain, GregoryWalker, SusanWalker, SusanWalker, SusanEgger, GeraldEgger, GeraldEgger, GeraldThiruvahindrapuram, BhoomaThiruvahindrapuram, BhoomaThiruvahindrapuram, BhoomaMerico, DanieleMerico, DanieleMerico, DanielePrasad, AparnaPrasad, AparnaPrasad, AparnaAnagnostou, EvdokiaAnagnostou, EvdokiaAnagnostou, EvdokiaFombonne, EricFombonne, EricFombonne, EricZwaigenbaum, LonnieZwaigenbaum, LonnieZwaigenbaum, LonnieRoberts, WendyRoberts, WendyRoberts, WendySzatmari, PeterSzatmari, PeterSzatmari, PeterFernandez, Bridget AFernandez, BridgetFernandez, Bridget AGeorgieva, LyudmilaGeorgieva, LyudmilaGeorgieva, LyudmilaBrzustowicz, LindaBrzustowicz, Linda MBrzustowicz, Linda MRoetzer, KatharinaRoetzer, KatharinaRoetzer, KatharinaKaschnitz, WolfgangKaschnitz, WolfgangKaschnitz, WolfgangVincent, John BVincent, John BVincent, John BWindpassinger, ChristianWindpassinger, ChristianWindpassinger, ChristianMarshall, Christian RMarshall, Christian RMarshall, Christian RTrifiletti, Rosario RTrifiletti, Rosario RTrifiletti, Rosario RKirmani, SalmanKirmani, SalmanKirmani, SalmanKirov, GeorgeKirov, GeorgeKirov, GeorgePetek, ErwinPetek, ErwinPetek, ErwinHodge, Jennelle CHodge, Jennelle CHodge, Jennelle CBassett, Anne SBassett, AnneBassett, Anne SScherer, Stephen WScherer, Stephen W and Scherer, Stephen W
Human molecular genetics, vol. 22, (no. 10), pp. 2066, 2013-May-15. | Journal Article
 
Response to Cobben et al. “Array CGH on unstimulated blood does not detect all cases of Pallister‐Killian Syndrome: Buccal smear analysis should remain the diagnostic procedure of first choice”
Hodge, Jennelle C and Kirmani, Salman
American Journal of Medical Genetics Part A, vol. 161, (no. 6), pp. 1521, June 2013. | Journal Article
2012
ALK alterations in adult renal cell carcinoma: frequency, clinicopathologic features and outcome in a large series of consecutively treated patients
Sukov, William RSukov, William RHodge, Jennelle CHodge, Jennelle CLohse, Christine MLohse, Christine MAkre, Monica KAkre, Monica KLeibovich, Bradley CLeibovich, Bradley CThompson, R HoustonThompson, R HCheville, John C and Cheville, John C
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, vol. 25, (no. 11), pp. 1525, 2012-Nov. | Journal Article
 
Array CGH on unstimulated blood does not detect all cases of Pallister–Killian syndrome: A skin biopsy should remain the diagnostic gold standard
Hodge, Jennelle CHodge, Jennelle CHulshizer, Rachael LHulshizer, Rachael LSeger, PamSeger, PamSt Antoine, AngeliqueSt Antoine, AngeliqueBair, JenniferBair, JenniferKirmani, Salman and Kirmani, Salman
American Journal of Medical Genetics Part A, vol. 158A, (no. 3), pp. 673, March 2012. | Journal Article
 
Atlas of Cytogenomics in Oncology and Hematology: a Platform-Neutral Clinical Cancer Genomics Database
Xiang, BixiaXiang, BixiaXiang, BixiaXiang, BixiaXiang, BixiaLeon, AnnetteLeon, AnnetteLeon, AnnetteLeon, AnnetteLeon, AnnetteLi, MarilynLi, MarilynLi, MarilynLi, MarilynLi, MarilynIqbal, AnwarIqbal, AnwarIqbal, AnwarIqbal, AnwarIqbal, AnwarLi, PeiningLi, PeiningLi, PeiningLi, PeiningLi, PeiningLi, ShiboLi, ShiboLi, ShiboLi, ShiboLi, ShiboPapenhausen, PeterPapenhausen, PeterPapenhausen, PeterPapenhausen, PeterPapenhausen, PeterSchwartz, StuartSchwartz, StuartSchwartz, StuartSchwartz, StuartSchwartz, StuartZhang, Xiao-XiangZhang, Xiao-XiangZhang, Xiao-XiangZhang, Xiao-XiangZhang, Xiao-XiangGeiersbach, KatherineGeiersbach, KatherineGeiersbach, KatherineGeiersbach, KatherineGeiersbach, KatherineSouth, SarahSouth, SarahSouth, SarahSouth, SarahSouth, SarahGu, GuangyuGu, GuangyuGu, GuangyuGu, GuangyuGu, GuangyuBatanian, JacquelineBatanian, JacquelineBatanian, JacquelineBatanian, JacquelineBatanian, JacquelineLu, XinyanLu, XinyanLu, XinyanLu, XinyanLu, XinyanWolff, DaynnaWolff, DaynnaWolff, DaynnaWolff, DaynnaWolff, DaynnaZnoyko, IyaZnoyko, IyaZnoyko, IyaZnoyko, IyaZnoyko, IyaLuthra, RajyalakshmiLuthra, RajyalakshmiLuthra, RajyalakshmiLuthra, RajyalakshmiLuthra, RajyalakshmiChen, SuChen, SuChen, SuChen, SuChen, SuPatel, KeyurPatel, KeyurPatel, KeyurPatel, KeyurPatel, KeyurSargent, RachelSargent, RachelSargent, RachelSargent, RachelSargent, RachelNaeem, RizwanNaeem, RizwanNaeem, RizwanNaeem, RizwanNaeem, RizwanShao, LinaShao, LinaShao, LinaShao, LinaShao, LinaBajaj, RenuBajaj, RenuBajaj, RenuBajaj, RenuBajaj, RenuPeiper, StephenPeiper, StephenPeiper, StephenPeiper, StephenPeiper, StephenWang, Zi-Xuan (Zoe)Wang, Zi-Xuan (Zoe)Wang, Zi-Xuan (Zoe)Wang, Zi-Xuan (Zoe)Wang, Zi-Xuan (Zoe)Smolarek, TeresaSmolarek, TeresaSmolarek, TeresaSmolarek, TeresaSmolarek, TeresaJenkins, LaurenJenkins, LaurenJenkins, LaurenJenkins, LaurenJenkins, LaurenLi, XuLi, XuLi, XuLi, XuLi, XuLi, FengLi, FengLi, FengLi, FengLi, FengWei, SainanWei, SainanWei, SainanWei, SainanWei, SainanHodge, JennelleHodge, JennelleHodge, JennelleHodge, JennelleHodge, JennelleMurata-Collins, JoyceMurata-Collins, JoyceMurata-Collins, JoyceMurata-Collins, JoyceMurata-Collins, JoyceChe, ZhiweiChe, ZhiweiChe, ZhiweiChe, ZhiweiChe, ZhiweiAhmad, AusafAhmad, AusafAhmad, AusafAhmad, AusafAhmad, AusafQi, MingQi, MingQi, MingQi, MingQi, MingForman, StephenForman, StephenForman, StephenForman, StephenForman, StephenVance, GailVance, GailVance, GailVance, GailVance, GailBest, RobertBest, RobertBest, RobertBest, Robert and Best, Robert
Cancer Genetics, vol. 205, (no. 7), pp. 420, 2012. | Journal Article