부산대학교 도서관

Rüschendorf, Ludger (D-FRBG-NDM) AMS Author Profile; Vanduffel, Steven (B-VUB-SB) AMS Author Profile; Bernard, Carole (F-GEM) AMS Author Profile

Sarah Grosche; Ingo Marenholz; Jorge Esparza-Gordillo; Aleix Arnau-Soler; Erola Pairo-Castineira; Franz Rüschendorf; Tarunveer S. Ahluwalia; Catarina Almqvist; Andreas Arnold; Australian Asthma Genetics Consortium (AAGC); Hansjörg Baurecht; Hans Bisgaard; Klaus Bønnelykke; Sara J. Brown; Mariona Bustamante; John A. Curtin; Adnan Custovic; Shyamali C. Dharmage; Ana Esplugues; Mario Falchi; Dietmar Fernandez-Orth; Manuel A. R. Ferreira; Andre Franke; Sascha Gerdes; Christian Gieger; Hakon Hakonarson; Patrick G. Holt; Georg Homuth; Norbert Hubner; Pirro G. Hysi; Marjo-Riitta Jarvelin; Robert Karlsson; Gerard H. Koppelman; Susanne Lau; Manuel Lutz; Patrik K. E. Magnusson; Guy B. Marks; Martina Müller-Nurasyid; Markus M. Nöthen; Lavinia Paternoster; Craig E. Pennell; Annette Peters; Konrad Rawlik; Colin F. Robertson; Elke Rodriguez; Sylvain Sebert; Angela Simpson; Patrick M. A. Sleiman; Marie Standl; Dora Stölzl; Konstantin Strauch; Agnieszka Szwajda; Albert Tenesa; Philip J. Thompson; Vilhelmina Ullemar; Alessia Visconti; Judith M. Vonk; Carol A. Wang; Stephan Weidinger; Matthias Wielscher; Catherine L. Worth; Chen-Jian Xu; Young-Ae Lee

Nature Communications, Vol 12, Iss 1, Pp 1-11 (2021)

Bernard, Carole (F-GEM-ALF) AMS Author Profile; Chen, Jinghui (B-VUB-BS) AMS Author Profile; Rüschendorf, Ludger (D-FRBG-DST); Vanduffel, Steven (B-VUB-BS)

Statistics \& Probability Letters (Statist. Probab. Lett.) (20230101), 199, Paper No 109853, 8 pp. ISSN: 0167-7152 (print).eISSN: 1879-2103.

Faugeras, Olivier P. (F-TOUL-SEC) AMS Author Profile; Rüschendorf, Ludger (D-FRBG) AMS Author Profile

Journal of Multivariate Analysis (J. Multivariate Anal.) (20210101), 186, Paper No 104802, 16 pp. ISSN: 0047-259X (print).eISSN: 1095-7243.

Ferreira MAR; Vonk JM; Baurecht H; Marenholz I; Tian C; Hoffman JD; Helmer Q; Tillander A; Ullemar V; Lu Y; Rüschendorf F; Hinds DA; Hübner N; Weidinger S; Magnusson PKE; Jorgenson E; Lee YA; Boomsma DI; Karlsson R; Almqvist C; Koppelman GH; Paternoster L

the 23 and Me Research Team & the collaborators of the SHARE study 2018, 'Eleven loci with new reproducible genetic associations with allergic disease risk', Journal of Allergy and Clinical Immunology. https://doi.org/10.1016/j.jaci.2018.03.012

Susgun S; Department of Biology, Chungnam National University, Daejeon 34134, Republic of Korea.; Department of Genetics, Aziz Sancar Institute of Experimental Medicine, Istanbul University, Istanbul, Türkiye.; Ben-Mahmoud A; Neurological Disorders Research Center, Qatar Biomedical Research Institute, Hamad Bin Khalifa University, Doha, Qatar.; Rüschendorf F; Max Delbrück Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany.; Ku B; Disease Target Structure Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon 34141, Republic of Korea.; Hussain SI; Department of Biotechnology and Genetic Engineering, Kohat University of Science & Technology (KUST), Kohat, Khyber Pakhtunkhwa, Pakistan.; Schulz S; Zentrum für Humangenetik, Tübingen, Germany.; Puk O; Zentrum für Humangenetik, Tübingen, Germany.; Biskup S; Zentrum für Humangenetik, Tübingen, Germany.; Center for Genomics and Transcriptomics (CeGaT), Tübingen, Germany.; Labonne JDJ; SalioGen Therapeutics, Lexington, MA, USA.; Don DW; Department of Biology, Chungnam National University, Daejeon 34134, Republic of Korea.; Gupta V; Neurological Disorders Research Center, Qatar Biomedical Research Institute, Hamad Bin Khalifa University, Doha, Qatar.; Choi TI; Department of Biology, Chungnam National University, Daejeon 34134, Republic of Korea.; Khan S; Department of Biotechnology and Genetic Engineering, Kohat University of Science & Technology (KUST), Kohat, Khyber Pakhtunkhwa, Pakistan.; Wasif N; Institute of Human Genetics, University of Ulm, Ulm, Germany.; Institute of Human Genetics, University Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany.; Lacassie Y; Department of Pediatrics, Louisiana State University Health Sciences Center, New Orleans, LA, USA.; Layman LC; Section of Reproductive Endocrinology, Infertility and Genetics, Department of Obstetrics and Gynecology, Augusta University, Augusta, GA, USA.; Department of Neuroscience and Regenerative Medicine, Augusta University, Augusta, GA, USA.; Ugur Iseri SA; Department of Genetics, Aziz Sancar Institute of Experimental Medicine, Istanbul University, Istanbul, Türkiye.; Kim CH; Department of Biology, Chungnam National University, Daejeon 34134, Republic of Korea.; Kim HG; Neurological Disorders Research Center, Qatar Biomedical Research Institute, Hamad Bin Khalifa University, Doha, Qatar.; College of Health and Life Sciences, Hamad Bin Khalifa University, Doha, Qatar.

Publisher: Wiley-Liss Country of Publication: United States NLM ID: 9215429 Publication Model: eCollection Cited Medium: Internet ISSN: 1098-1004 (Electronic) Linking ISSN: 10597794 NLM ISO Abbreviation: Hum Mutat Subsets: MEDLINE

Møller, R. S.; Weber, Y. G.; Klitten, L. L.; Trucks, H.; Muhle, H.; Kunz, W. S.; Mefford, H. C.; Franke, A.; Kautza, M.; Wolf, P.; Dennig, D.; Schreiber, S.; Rückert, I. -.M.; Wichmann, H. -.E.; Ernst, J. P.; Schurmann, C.; Grabe, H. J.; Tommerup, N.; Stephani, U.; Lerche, H.; Hjalgrim, H.; Helbig, I.; Sander, T.; Zimprich, F.; Mörzinger, M.; Feucht, M.; Suls, A.; Weckhuysen, S.; Claes, L.; Deprez, L.; Smets, K.; Van Dyck, T.; Deconinck, T.; De Jonghe, P.; Velizarova, R.; Dimova, P.; Radionova, M.; Tournev, I.; Kancheva, D.; Kaneva, R.; Jordanova, A.; Kjelgaard, D. B.; Lehesjoki, A. -.E.; Siren, A.; Baulac, S.; Leguern, E.; Von Spiczak, S.; Ostertag, P.; Leber, M.; Leu, C.; Toliat, M. R.; Nürnberg, P.; Hempelmann, A.; Rüschendorf, F.; Elger, C. E.; Kleefuß-lie, A. A.; Surges, R.; Gaus, V.; Janz, D.; Schmitz, B.; Klein, K. M.; Reif, P. S.; Oertel, W. H.; Hamer, H. M.; Rosenow, F.; Becker, F.; Marini, C.; Guerrini, R.; Mei, D.; Norci, V.; Zara, F.; Striano, P.; Robbiano, A.; Pezzella, M.; Bianchi, A.; Gambardella, A.; Tinuper, P.; La Neve, A.; Capovilla, G.; Vigliano, P.; Crichiutti, G.; Vanadia, F.; Vignoli, A.; Coppola, A.; Striano, S.; Giallonardo, M. T.; Franceschetti, S.; Belcastro, V.; Benna, P.; Coppola, G.; De Palo, A.; Ferlazzo, E.; Vecchi, M.; Martinelli, V.; Bisulli, F.; Beccaria, F.; Del Giudice, E.; Mancardi, M.; Stranci, G.; Scabar, A.; Gobbi, G.; Giordano, I.; Koeleman, B. P. C.; De Kovel, C.; Lindhout, D.; De Haan, G. -.J.; Ozbeck, U.; Bebek, N.; Baykan, B.; Ozdemir, O.; Ugur, S.; Kocasoy-orhan, E.; Yücesan, E.; Cine, N.; Gokyigit, A.; Gurses, C.; Gul, G.; Yapici, Z.; Ozkara, C.; Caglayan, H.; Yalcin, O.; Yalcin, D.; Turkdogan, D.; Dizdarer, G.; Agan, K.

Møller, R S, YG, W, Klitten, L L, H, T, H, M, WS, K, HC, M, A, F, M, K, P, W, D, D, S, S, IM, R, HE, W, JP, E, C, S, HJ, G, N, T, U, S, H, L, Hjalgrim, H, I, H & T, S 2013, ' Exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsy ', Epilepsia, vol. 54, no. 2, pp. 256-264 . https://doi.org/10.1111/epi.12078

Steffens M.; Leu C.; Ruppert A.; Zara F.; Striano P.; Robbiano A.; Capovilla G.; Tinuper P.; Gambardella A.; Bianchi A.; La neve A.; Crichiutti G.; de kovel C. G.; Trenité D. K. -N.; de haan G.; Lindhout D.; Gaus V.; Schmitz B.; Janz D.; Weber Y. G.; Becker F.; Lerche H.; Steinhoff B. J.; Kleefuß-Lie A. A.; Kunz W. S.; Surges R.; Elger C. E.; Muhle H.; Von spiczak S.; Ostertag P.; Helbig I.; Stephani U.; Møller R. S.; Hjalgrim H.; Dibbens L. M.; Bellows S.; Oliver K.; Mullen S.; Scheffer I. E.; Berkovic S. F.; Everett K. V.; Gardiner M. R.; MARINI, CHIARA; Guerrini R.; Lehesjoki A.; Siren A.; Guipponi M.; Malafosse A.; Thomas P.; Nabbout R.; Baulac S.; Leguern E.; Guerrero R.; Serratosa J. M.; Reif P. S.; Rosenow F.; Mörzinger M.; Feucht M.; Zimprich F.; Kapser C.; Schankin C. J.; Suls A.; Smets K.; De jonghe P.; Jordanova A.; Caglayan H.; Yapici Z.; Yalcin D. A.; Baykan B.; Bebek N.; Ozbek U.; Gieger C.; Wichmann H.; Balschun T.; Ellinghaus D.; Franke A.; Meesters C.; Becker T.; Wienker T. F.; Hempelmann A.; Schulz H.; Rüschendorf F.; Leber M.; Pauck S. M.; Trucks H.; Toliat M. R.; Nürnberg P.; Avanzini G.; Koeleman B. P.; Sander T.; Weckhuysen S.; Claes L.; Deprez L.; Van Dyck T.; Deconinck T.; De Jonghe P.; Velizarova R.; Dimova P.; Radionova M.; Tournev I.; Kancheva D.; Kaneva R.; Lehesjoki A. -E.; von Spiczak S.; Martin Klein K.; Oertel W. H.; Hamer H. M.; Marini C.; Mei D.; Norci V.; Pezzella M.; La Neve A.; Vigliano P.; Vanadia F.; Vignoli A.; Coppola A.; Striano S.; Egeo G.; Teresa Giallonardo M.; Franceschetti S.; Belcastro V.; Benna P.; Coppola G.; De Palo A.; Ferlazzo E.; Vecchi M.; Martinelli V.; Bisulli F.; Beccaria F.; Del Giudice E.; Mancardi M.; Stranci G.; Scabar A.; Gobbi G.; Giordano I.; de Haan G. -J.; Giraldez B. G.; Ozbeck U.; Ozdemir O.; Ugur S.; Kocasoy-Orhan E.; Yücesan E.; Cine N.; Gokyigit A.; Gurses C.; Gul G.; Ozkara C.; Yalcin O.; Turkdogan D.; Dizdarer G.; Agan K.

Human molecular genetics 21(24), 5359-5372 (2012). doi:10.1093/hmg/dds373
Human Molecular Genetics
Steffens, M, Leu, C, Ruppert, A K, Zara, F, Striano, P, Robbiano, A, Capovilla, G, Tinuper, P, Gambardella, A, Bianchi, A, La Neve, A, Crichiutti, G, de Kovel, C G F, Trenite, D K N, de Haan, G J, Lindhout, D, Gaus, V, Schmitz, B, Janz, D, Weber, Y G, Becker, F, Lerche, H, Steinhoff, B J, Kleefuss-Lie, A A, Kunz, W S, Surges, R, Elger, C E, Muhle, H, von Spiczak, S, Ostertag, P, Helbig, I, Stephani, U, Moller, R S, Hjalgrim, H, Dibbens, L M, Bellows, S, Oliver, K, Mullen, S, Scheffer, I E, Berkovic, S F, Everett, K V, Gardiner, M R, Marini, C, Guerrini, R, Lehesjoki, A E, Siren, A K, Guipponi, M, Malafosse, A, Thomas, P, Nabbout, R, Baulac, S, Leguern, E, Guerrero, R, Serratosa, J M, Reif, P S, Rosenow, F, Morzinger, M, Feucht, M, Zimprich, F, Kapser, C, Schankin, C J, Suls, A, Smets, K, De Jonghe, P, Jordanova, A, Caglayan, H, Yapici, Z, Yalcin, D A, Baykan, B, Bebek, N, Ozbek, U, Gieger, C, Wichmann, H E, Balschun, T, Ellinghaus, D, Franke, A, Meesters, C, Becker, T, Wienker, T F, Hempelmann, A, Schulz, H, Ruschendorf, F, Leber, M, Pauck, S M, Trucks, H, Toliat, M R, Nurnberg, P, Avanzini, G, Koeleman, B P C, Sander, T, Consortium, E & Consortium, E 2012, ' Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32 ', Human Molecular Genetics, vol. 21, no. 24, pp. 5359-5372 . https://doi.org/10.1093/hmg/dds373

Leu C; de Kovel CG; Zara F; Striano P; Pezzella M; Robbiano A; Bianchi A; Bisulli F; Coppola A; Giallonardo AT; Beccaria F; Trenité DK; Lindhout D; Gaus V; Schmitz B; Janz D; Weber YG; Becker F; Lerche H; Kleefuss Lie AA; Hallman K; Kunz WS; Elger CE; Muhle H; Stephani U; Møller RS; Hjalgrim H; Mullen S; Scheffer IE; Berkovic SF; Everett KV; Gardiner MR; Marini C; Guerrini R; Lehesjoki AE; Siren A; Nabbout R; Baulac S; Leguern E; Serratosa JM; Rosenow F; Feucht M; Unterberger I; Covanis A; Suls A; Weckhuysen S; Kaneva R; Caglayan H; Turkdogan D; Baykan B; Bebek N; Ozbek U; Hempelmann A; Schulz H; Rüschendorf F; Trucks H; Nürnberg P; Avanzini G; Koeleman BP; Sander T; EPICURE Consortium; DEL GIUDICE, ENNIO; COPPOLA, ANTONIETTA

Leu, C, de Kovel, C G F, Zara, F, Striano, P, Pezzella, M, Robbiano, A, Bianchi, A, Bisulli, F, Coppola, A, Giallonardo, A T, Beccaria, F, Trenité, D K-N, Lindhout, D, Gaus, V, Schmitz, B, Janz, D, Weber, Y G, Becker, F, Lerche, H, Kleefuss-Lie, A A, Hallman, K, Kunz, W S, Elger, C E, Muhle, H, Stephani, U, Møller, R S, Hjalgrim, H, Mullen, S, Scheffer, I E, Berkovic, S F, Everett, K V, Gardiner, M R, Marini, C, Guerrini, R, Lehesjoki, A-E, Siren, A, Nabbout, R, Baulac, S, Leguern, E, Serratosa, J M, Rosenow, F, Feucht, M, Unterberger, I, Covanis, A, Suls, A, Weckhuysen, S, Kaneva, R, Caglayan, H, Turkdogan, D, Baykan, B & EPICURE Consortium 2012, ' Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies ', Epilepsia, vol. 53, no. 2, pp. 308-318 . https://doi.org/10.1111/j.1528-1167.2011.03379.x

Simaite, D.; Kofent, J.; Gong, M.; Rüschendorf, F.; Jia, S.; Arn, P.; Bentler, K.; Ellaway, C.; Kühnen, P.; Hoffmann, G.F.; Blau, N.; Spagnoli, Francesca M.; Hübner, N.; Raile, K.

Diabetes. 63:3557-3564

Waage, J; Standl, M; Curtin, JA; Jessen, LE; Thorsen, J; Tian, C; Schoettler, N; 23andMe Research Team; AAGC collaborators; Flores, C; Abdellaoui, A; Ahluwalia, TS; Alves, AC; Amaral, AFS; Antó, JM; Arnold, A; Barreto-Luis, A; Baurecht, H; van Beijsterveldt, CEM; Bleecker, ER; Bonàs-Guarch, S; Boomsma, DI; Brix, S; Bunyavanich, S; Burchard, EG; Chen, Z; Curjuric, I; Custovic, A; den Dekker, HT; Dharmage, SC; Dmitrieva, J; Duijts, L; Ege, MJ; Gauderman, WJ; Georges, M; Gieger, C; Gilliland, F; Granell, R; Gui, H; Hansen, T; Heinrich, J; Henderson, J; Hernandez-Pacheco, N; Holt, P; Imboden, M; Jaddoe, VWV; Jarvelin, M-R; Jarvis, DL; Jensen, KK; Jónsdóttir, I; Kabesch, M; Kaprio, J; Kumar, A; Lee, Y-A; Levin, AM; Li, X; Lorenzo-Diaz, F; Melén, E; Mercader, JM; Meyers, DA; Myers, R; Nicolae, DL; Nohr, EA; Palviainen, T; Paternoster, L; Pennell, CE; Pershagen, G; Pino-Yanes, M; Probst-Hensch, NM; Rüschendorf, F; Simpson, A; Stefansson, K; Sunyer, J; Sveinbjornsson, G; Thiering, E; Thompson, PJ; Torrent, M; Torrents, D; Tung, JY; Wang, CA; Weidinger, S; Weiss, S; Willemsen, G; Williams, LK; Ober, C; Hinds, DA; Ferreira, MA; Bisgaard, H; Strachan, DP; Bønnelykke, K

Huck, K; Feyen, O; Niehues, T; Rüschendorf, F; Hübner, N; Laws, H; Telieps, T; Knapp, S; Wacker, H; Meindl, A; Jumaa, H; Borkhardt, A

Journal of Clinical Investigation. 119:1350-1358

Rüschendorf, F.; Fuchshuber, A.; Kroiss, S.; Karle, S.; Berthold, S.; Huck, K.; Burton, C.; Rahman, N.; Koptides, Michael; Constantinou-Deltas, Constantinos D.; Otto, E.; Feest, T.; Hildebrandt, F.

Genomics

Bayer, Y.; Neumann, S.; Meyer, B.; Rüschendorf, F.; Reske, A.; Brix, T.H.; Hegedüs, Laszlo; Langer, Pavel; Nürnberg, Peter; Paschke, Ralf

The Journal of Clinical Endocrinology & Metabolism. 89:4044-4052

Kurz, Thorsten, MSc; Strauch, Konstantin, MA; Heinzmann, Andrea, MD; Braun, Sandra; Jung, Martin, PhD; Rüschendorf, Franz, PhD; Moffatt, Miriam F., DPhil; Cookson, William O.C.M., MD, DPhil; Inacio, Filipe, MD; Ruffilli, Anna, PhD; Nordskov-Hansen, Gitte, BSc; Peltre, Gabriel, PhD; Forster, Johannes, MD; Kuehr, Joachim, MD; Reis, André, MD; Wienker, Thomas F., MD; Deichmann, Klaus A., MD

The Journal of Allergy and Clinical Immunology. 106(5):925-932

Hensen, P; Windemuth, C; Hüffmeier, U; Rüschendorf, F; Stadelmann, A; Hoppe, V; Fenneker, D; Ständer, M; Schmitt-Egenolf, Marcus; Wienker, TF; Traupe, H; Reis, A

Experimental dermatology. 12(4):490-496

Hensen, P; Asadullah, K; Windemuth, C; Rüschendorf, F; Hüffmeier, U; Ständer, M; Schmitt-Egenolf, Marcus; Wienker, TF; Reis, A; Traupe, H

British Journal of Dermatology. 149(2):381-385

Lin SJ; Genes & Human Disease Research Program, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma, USA.; Vona B; Institute of Human Genetics, Julius Maximilians University Würzburg, Würzburg, Germany.; Institute for Auditory Neuroscience and InnerEarLab, University Medical Center Göttingen, Göttingen, Germany.; Institute of Human Genetics, University Medical Center Göttingen, Göttingen, Germany.; Porter HM; Children's National Hospital, Rare Disease Institute, Washington, District of Columbia, USA.; Izadi M; Division of Genomics and Translational Medicine, College of Health and Life Sciences, Hamad Bin Khalifa University, Doha, Qatar.; Huang K; Genes & Human Disease Research Program, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma, USA.; Lacassie Y; Department of Pediatrics, Louisiana State University Health Sciences Center, Head Division of Clinical Genetics and Dept. of Genetics Children's Hospital 1986-2016, New Orleans, Los Angeles, USA.; Rosenfeld JA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Baylor Genetics Laboratories, Houston, Texas, USA.; Khan S; Department of Biotechnology and Genetic Engineering, Kohat University of Science & Technology, Kohat, Khyber Pakhtunkhwa, Pakistan.; Petree C; Genes & Human Disease Research Program, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma, USA.; Ali TA; Division of Genomics and Translational Medicine, College of Health and Life Sciences, Hamad Bin Khalifa University, Doha, Qatar.; Muhammad N; Department of Biotechnology and Genetic Engineering, Kohat University of Science & Technology, Kohat, Khyber Pakhtunkhwa, Pakistan.; Khan SA; Department of Biotechnology and Genetic Engineering, Kohat University of Science & Technology, Kohat, Khyber Pakhtunkhwa, Pakistan.; Muhammad N; Department of Biotechnology and Genetic Engineering, Kohat University of Science & Technology, Kohat, Khyber Pakhtunkhwa, Pakistan.; Liu P; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Baylor Genetics Laboratories, Houston, Texas, USA.; Haymon ML; Children Hospital New Orleans Louisiana, Pediatric Radiology, Tulane Associate Professor of Radiology, New Orleans, Los Angeles, USA.; Rüschendorf F; Max Delbrück Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany.; Kong IK; Department of Animal Sciences, Division of Applied Life Science (BK21 Four), Gyeongsang National University, Jinju, South Korea.; Schnapp L; Institute of Human Genetics, Julius Maximilians University Würzburg, Würzburg, Germany.; Shur N; Children's National Hospital, Rare Disease Institute, Washington, District of Columbia, USA.; Chorich L; Section of Reproductive Endocrinology, Infertility & Genetics, Department of Obstetrics and Gynecology, Department of Neuroscience and Regenerative Medicine, Medical College of Georgia, Augusta University, Augusta, USA.; Layman L; Section of Reproductive Endocrinology, Infertility & Genetics, Department of Obstetrics and Gynecology, Department of Neuroscience and Regenerative Medicine, Medical College of Georgia, Augusta University, Augusta, USA.; Haaf T; Institute of Human Genetics, Julius Maximilians University Würzburg, Würzburg, Germany.; Pourkarimi E; Division of Genomics and Translational Medicine, College of Health and Life Sciences, Hamad Bin Khalifa University, Doha, Qatar.; Kim HG; Neurological Disorders Research Center, Qatar Biomedical Research Institute, Hamad Bin Khalifa University, Doha, Qatar.; Varshney GK; Genes & Human Disease Research Program, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma, USA.

Publisher: Wiley-Liss Country of Publication: United States NLM ID: 9215429 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1098-1004 (Electronic) Linking ISSN: 10597794 NLM ISO Abbreviation: Hum Mutat Subsets: MEDLINE

Lee, YA; Rüschendorf, F; Windemuth, C; Schmitt-Egenolf, Marcus; Stadelmann, A; Nürnberg, G; Ständer, M; Wienker, TF; Reis, A; Traupe, H

American Journal of Human Genetics. 67(4):1020-1024

Auer, F.; Rüschendorf, F.; Gombert, Michael; Husemann, Peter; Ginzel, Sebastian; Izraeli, S.; Harit, M.; Weintraub, M.; Weinstein, O. Y.; Lerer, I.; Stepensky, P.; Borkhardt, Arndt; Hauer, J.

Leukemia. 28:1136-1138