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Michael Knapp

University of Pittsburgh School of Medicine

53H指数
240论文数
1.0W被引数
收录论文 83
发表时间
Tibial Vein Thrombosis After Foam Sclerotherapy: A Single Institution Case Series泡沫硬化疗法后的胫后静脉血栓形成:单中心病例系列
err2025-09-19
err0
PREAI
errJack K. Donohue; Emily Mosher; Michael Knapp; Nuzhat Kabir; Nishant Agrawal; Robert Handzel; Natalie D. Sridharan; Eric S. Hager
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Point- of-Care Ultrasound Estimation of Right Atrial Pressure Predicts Early Readmission in Patients With Acute Decompensated Heart Failure
err2023-11-07
err0
PREAI
errKnapp, Michael; Aluko, Oluwatosin; Chapagain, Himal; Faizee, Faizan; Kainat, Aleesha; Chaudhary, Rahul; Simon, Marc A.; Pacella, John
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Dissecting the genetic heterogeneity of gastric cancer
err2023-06-01
err9
errOAAI
errHess, Timo; Maj, Carlo; Gehlen, Jan; Borisov, Oleg; Haas, Stephan L.; Gockel, Ines; Vieth, Michael; Piessen, Guillaume; Alakus, Hakan; Vashist, Yogesh; Pereira, Carina; Knapp, Michael; Schueller, Vitalia; Quaas, Alexander; Grabsch, Heike I.; Trautmann, Jessica; Malecka-Wojciesko, Ewa; Mokrowiecka, Anna; Speller, Jan; Mayr, Andreas; Schroeder, Julia; Hillmer, Axel M.; Heider, Dominik; Lordick, Florian; Perez-Aisa, Angeles; Campo, Rafael; Espinel, Jesus; Geijo, Fernando; Thomson, Concha; Bujanda, Luis; Sopena, Federico; Lanas, Angel; Pellise, Maria; Pauligk, Claudia; Goetze, Thorsten Oliver; Zelck, Carolin; Reingruber, Julian; Hassanin, Emadeldin; Elbe, Peter; Alsabeah, Sandra; Lindblad, Mats; Nilsson, Magnus; Kreuser, Nicole; Thieme, Rene; Tavano, Francesca; Pastorino, Roberta; Arzani, Dario; Persiani, Roberto; Jung, Jin-On; Nienhueser, Henrik; Ott, Katja; Schumann, Ralf R.; Kumpf, Oliver; Burock, Susen; Arndt, Volker; Jakubowska, Anna; Lawniczak, Malgorzta; Dabrowska, Justyna; Cussenot, Olivier; Boland-Auge, Anne; Daian, Delphine; Deleuze, Jean-Francois; Salvi, Erika; Teder-Laving, Maris; Tomasello, Gianluca; Ratti, Margherita; Senti, Chiara; De Re, Valli; Steffan, Agostino; Hoelscher, Arnulf H.; Messerle, Katharina; Bruns, Christiane Josephine; Sivins, Armands; Bogdanova, Inga; Skieceviciene, Jurgita; Arstikyte, Justina; Moehler, Markus; Lang, Hauke; Grimminger, Peter P.; Kruschewski, Martin; Vassos, Nikolaos; Schildberg, Claus; Lingohr, Philipp; Ridwelski, Karsten; Lippert, Hans; Fricker, Nadine; Krawitz, Peter; Hoffmann, Per; Noethen, Markus M.; Veits, Lothar; Izbicki, Jakob R.; Mostowska, Adrianna; Martinon-Torres, Federico; Cusi, Daniele; Adolfsson, Rolf; Cancel-Tassin, Geraldine; Hoeblinger, Aksana; Rodermann, Ernst; Ludwig, Monika; Keller, Gisela; Metspalu, Andres; Brenner, Hermann; Heller, Joerg; Neef, Markus; Schepke, Michael; Dumoulin, Franz Ludwig; Hamann, Lutz; Cannizzaro, Renato; Ghidini, Michele; Plassmann, Dominik; Geppert, Michael; Malfertheiner, Peter; Gehlen, Olivier; Skoczylas, Tomasz; Majewski, Marek; Lubinski, Jan; Palmieri, Orazio; Boccia, Stefania; Latiano, Anna; Aragones, Nuria; Schmidt, Thomas; Dinis-Ribeiro, Mario; Medeiros, Rui; Al-Batran, Salah-Eddin; Leja, Marcis; Kupcinskas, Juozas; Garcia-Gonzalez, Maria A.; Venerito, Marino; Schumachera, Johannes
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A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy
err2022-11-09
err4
errOAAI
errMingardo, Enrico; Beaman, Glenda; Grote, Philip; Nordenskjold, Agneta; Newman, William; Woolf, Adrian S.; Eckstein, Markus; Hilger, Alina C.; Dworschak, Gabriel C.; Roesch, Wolfgang; Ebert, Anne-Karolin; Stein, Raimund; Brusco, Alfredo; Di Grazia, Massimo; Tamer, Ali; Torres, Federico M.; Hernandez, Jose L.; Erben, Philipp; Maj, Carlo; Olmos, Jose M.; Riancho, Jose A.; Valero, Carmen; Hostettler, Isabel C.; Houlden, Henry; Werring, David J.; Schumacher, Johannes; Gehlen, Jan; Giel, Ann-Sophie; Buerfent, Benedikt C.; Arkani, Samara; Akesson, Elisabeth; Rotstein, Emilia; Ludwig, Michael; Holmdahl, Gundela; Giorgio, Elisa; Berettini, Alfredo; Keene, David; Cervellione, Raimondo M.; Younsi, Nina; Ortlieb, Melissa; Oswald, Josef; Haid, Bernhard; Promm, Martin; Neissner, Claudia; Hirsch, Karin; Stehr, Maximilian; Schafer, Frank-Mattias; Schmiedeke, Eberhard; Boemers, Thomas M.; van Rooij, Iris A. L. M.; Feitz, Wouter F. J.; Marcelis, Carlo L. M.; Lacher, Martin; Nelson, Jana; Ure, Benno; Fortmann, Caroline; Gale, Daniel P.; Chan, Melanie M. Y.; Ludwig, Kerstin U.; Noethen, Markus M.; Heilmann, Stefanie; Zwink, Nadine; Jenetzky, Ekkehart; Odermatt, Benjamin; Knapp, Michael; Reutter, Heiko
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eQTL Set-Based Association Analysis Identifies Novel Susceptibility Loci for Barrett Esophagus and Esophageal Adenocarcinoma基于eQTL集的关联分析确定了Barrett食管和食管腺癌的新易感位点
err2022-06-16
err4
errOAAI
errWang, Xiaoyu; Gharahkhani, Puya; Levine, David M.; Fitzgerald, Rebecca C.; Gockel, Ines; Corley, Douglas A.; Risch, Harvey A.; Bernstein, Leslie; Chow, Wong-Ho; Onstad, Lynn; Shaheen, Nicholas J.; Lagergren, Jesper; Hardie, Laura J.; Wu, Anna H.; Pharoah, Paul D. P.; Liu, Geoffrey; Anderson, Lesley A.; Iyer, Prasad G.; Gammon, Marilie D.; Caldas, Carlos; Ye, Weimin; Barr, Hugh; Moayyedi, Paul; Harrison, Rebecca; Watson, R. G. Peter; Attwood, Stephen; Chegwidden, Laura; Love, Sharon B.; MacDonald, David; DeCaestecker, John; Prenen, Hans; Ott, Katja; Moebus, Susanne; Venerito, Marino; Lang, Hauke; Mayershofer, Rupert; Knapp, Michael; Veits, Lothar; Gerges, Christian; Weismueller, Josef; Reeh, Matthias; Noethen, Markus M.; Izbicki, Jakob R.; Manner, Hendrik; Neuhaus, Horst; Roesch, Thomas; Boehmer, Anne C.; Hoelscher, Arnulf H.; Anders, Mario; Pech, Oliver; Schumacher, Brigitte; Schmidt, Claudia; Schmidt, Thomas; Noder, Tania; Lorenz, Dietmar; Vieth, Michael; May, Andrea; Hess, Timo; Kreuser, Nicole; Becker, Jessica; Ell, Christian; Tomlinson, Ian; Palles, Claire; Jankowski, Janusz A.; Whiteman, David C.; MacGregor, Stuart; Schumacher, Johannes; Vaughan, Thomas L.; Buas, Matthew F.; Dai, James Y.
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First genome-wide association study of esophageal atresia identifies three genetic risk loci at CTNNA3, FOXF1/FOXC2/FOXL1, and HNF1B
err2022-04-01
err5
errOAAI
errGehlen, Jan; Giel, Ann-Sophie; Koellges, Ricarda; Haas, Stephan L.; Zhang, Rong; Trcka, Jiri; Sungur, Ayse O.; Renziehausen, Florian; Bornholdt, Dorothea; Jung, Daphne; Hoyer, Paul D.; Nordenskjold, Agneta; Tibboel, Dick; Vlot, John; Spaander, Manon C. W.; Smigiel, Robert; Patkowski, Dariusz; Roeleveld, Nel; van Rooij, Iris Alm; de Blaauw, Ivo; Hoelscher, Alice; Pauly, Marcus; Leutner, Andreas; Fuchs, Joerg; Niethammer, Joel; Melissari, Maria-Theodora; Jenetzky, Ekkehart; Zwink, Nadine; Thiele, Holger; Hilger, Alina Christine; Hess, Timo; Trautmann, Jessica; Marks, Matthias; Baumgarten, Martin; Blaess, Gaby; Landen, Mikael; Fundin, Bengt; Bulik, Cynthia M.; Pennimpede, Tracie; Ludwig, Michael; Ludwig, Kerstin U.; Mangold, Elisabeth; Heilmann-Heimbach, Stefanie; Moebus, Susanne; Herrmann, Bernhard G.; Alsabeah, Kristina; Burgos, Carmen M.; Lilja, Helene E.; Azodi, Sahar; Stenstrom, Pernilla; Arnbjornsson, Einar; Frybova, Barbora; Lebensztejn, Dariusz M.; Debek, Wojciech; Kolodziejczyk, Elwira; Kozera, Katarzyna; Kierkus, Jaroslaw; Kalicinski, Piotr; Stefanowicz, Marek; Socha-Banasiak, Anna; Kolejwa, Michal; Piaseczna-Piotrowska, Anna; Czkwianianc, Elzbieta; Noethen, Markus M.; Grote, Phillip; Rygl, Michal; Reinshagen, Konrad; Spychalski, Nicole; Ludwikowski, Barbara; Hubertus, Jochen; Heydweiller, Andreas; Ure, Benno; Muensterer, Oliver J.; Aubert, Ophelia; Gosemann, Jan-Hendrik; Lacher, Martin; Degenhardt, Petra; Boemers, Thomas M.; Mokrowiecka, Anna; Malecka-Panas, Ewa; Woehr, Markus; Knapp, Michael; Seitz, Guido; de Klein, Annelies; Oracz, Grzegorz; Brosens, Erwin; Reutter, Heiko; Schumacher, Johannes
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Allele-specific transcription factor binding in a cellular model of orofacial clefting
err2022-02-02
err1
errOAAI
errRuff, Katharina L. M.; Hollstein, Ronja; Fazaal, Julia; Thieme, Frederic; Gehlen, Jan; Mangold, Elisabeth; Knapp, Michael; Welzenbach, Julia; Ludwig, Kerstin U.
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MiRNA-149 as a Candidate for Facial Clefting and Neural Crest Cell Migration
err2021-09-16
err10
errOAAI
errStuessel, L. G.; Hollstein, R.; Laugsch, M.; Hochfeld, L. M.; Welzenbach, J.; Schroeder, J.; Thieme, F.; Ishorst, N.; Romero, R. Olmos; Weinhold, L.; Hess, T.; Gehlen, J.; Mostowska, A.; Heilmann-Heimbach, S.; Mangold, E.; Rada-Iglesias, A.; Knapp, M.; Schaaf, C. P.; Ludwig, K. U.
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Integrative approaches generate insights into the architecture of non-syndromic cleft lip with or without cleft palate综合方法可洞悉有无腭裂的非综合征性唇裂的结构
err2021-07-01
err15
errOAAI
errWelzenbach, Julia; Hammond, Nigel L.; Nikolic, Milos; Thieme, Frederic; Ishorst, Nina; Leslie, Elizabeth J.; Weinberg, Seth M.; Beaty, Terri H.; Marazita, Mary L.; Mangold, Elisabeth; Knapp, Michael; Cotney, Justin; Rada-Iglesias, Alvaro; Dixon, Michael J.; Ludwig, Kerstin U.
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Germline variation in the insulin-like growth factor pathway and risk of Barrett's esophagus and esophageal adenocarcinoma
err2020-12-10
err10
errOAAI
errDighe, Shruti G.; Chen, Jianhong; Yan, Li; He, Qianchuan; Gharahkhani, Puya; Onstad, Lynn; Levine, David M.; Palles, Claire; Ye, Weimin; Gammon, Marilie D.; Iyer, Prasad G.; Anderson, Lesley A.; Liu, Geoffrey; Wu, Anna H.; Dai, James Y.; Chow, Wong-Ho; Risch, Harvey A.; Lagergren, Jesper; Shaheen, Nicholas J.; Bernstein, Leslie; Corley, Douglas A.; Prenen, Hans; DeCaestecker, John; MacDonald, David; Moayyedi, Paul; Barr, Hugh; Love, Sharon B.; Chegwidden, Laura; Attwood, Stephen; Watson, Peter; Harrison, Rebecca; Ott, Katja; Moebus, Susanne; Venerito, Marino; Lang, Hauke; Mayershofer, Rupert; Knapp, Michael; Veits, Lothar; Gerges, Christian; Weismueller, Josef; Gockel, Ines; Vashist, Yogesh; Noethen, Markus M.; Izbicki, Jakob R.; Manner, Hendrik; Neuhaus, Horst; Roesch, Thomas; Boehmer, Anne C.; Hoelscher, Arnulf H.; Anders, Mario; Pech, Oliver; Schumacher, Brigitte; Schmidt, Claudia; Schmidt, Thomas; Noder, Tania; Lorenz, Dietmar; Vieth, Michael; May, Andrea; Hess, Timo; Kreuser, Nicole; Becker, Jessica; Ell, Christian; Ambrosone, Christine B.; Moysich, Kirsten B.; MacGregor, Stuart; Tomlinson, Ian; Whiteman, David C.; Jankowski, Janusz; Schumacher, Johannes; Vaughan, Thomas L.; Madeleine, Margaret M.; Hardie, Laura J.; Buas, Matthew F.
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Introducing a new recruitment approach to sample collection for genetic association studies in opioid dependence
err2020-04-16
err8
PREAI
errFranke, P; Wendel, B; Knapp, M; Schwab, SG; Neef, D; Maier, W; Wildenauer, DB; Hoehe, MR
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Shared Genetic Etiology of Obesity-Related Traits and Barrett's Esophagus/Adenocarcinoma: Insights from Genome-Wide Association Studies
err2020-02-05
err6
PREAI
errBoehmer, Anne C.; Hecker, Julian; Schroeder, Julia; Gharahkhani, Puya; May, Andrea; Gerges, Christian; Anders, Mario; Becker, Jessica; Hess, Timo; Kreuser, Nicole; Thieme, Rene; Noder, Tania; Venerito, Marino; Veits, Lothar; Schmidt, Thomas; Fuchs, Claudia; Izbicki, Jakob R.; Hoelscher, Arnulf H.; Dietrich, Arne; Moulla, Yusef; Lyros, Orestis; Lang, Hauke; Lorenz, Dietmar; Schumacher, Brigitte; Mayershofer, Rupert; Vashist, Yogesh; Ott, Katja; Vieth, Michael; Meismueller, Josef; Moebus, Susanne; Knapp, Michael; Neuhaus, Horst; Roesch, Thomas; Ell, Christian; Noethen, Markus M.; Whiteman, David C.; Tomlinson, Ian; Jankowski, Janusz; Fitzgerald, Rebecca C.; Palles, Claire; Vaughan, Thomas L.; Gockel, Ines; Thrift, Aaron P.; Fier, Heide; Schumacher, Johannes
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Msx1 deficiency interacts with hypoxia and induces a morphogenetic regulation during mouse lip development
err2020-01-01
err18
errOAAI
errNakatomi, Mitsushiro; Ludwig, Kerstin U.; Knapp, Michael; Kist, Ralf; Lisgo, Steven; Ohshima, Hayato; Mangold, Elisabeth; Peters, Heiko
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No Association Between Vitamin D Status and Risk of Barrett's Esophagus or Esophageal Adenocarcinoma: A Mendelian Randomization Study维生素d状态与Barrett食管或食管腺癌风险之间无关联: 一项孟德尔随机化研究
err2019-10-01
err16
errOAAI
errDong, Jing; Gharahkhani, Puya; Chow, Wong-Ho; Gammon, Marilie D.; Liu, Geoffrey; Caldas, Carlos; Wu, Anna H.; Ye, Weimin; Onstad, Lynn; Anderson, Lesley A.; Bernstein, Leslie; Pharoah, Paul D.; Risch, Harvey A.; Corley, Douglas A.; Fitzgerald, Rebecca C.; Iyer, Prasad G.; Reid, Brian J.; Lagergren, Jesper; Shaheen, Nicholas J.; Vaughan, Thomas L.; MacGregor, Stuart; Love, Sharon; Palles, Claire; Tomlinson, Ian; Gockel, Ines; May, Andrea; Gerges, Christian; Anders, Mario; Bohmer, Anne C.; Becker, Jessica; Kreuser, Nicole; Thieme, Rene; Noder, Tania; Venerito, Marino; Veits, Lothar; Schmidt, Thomas; Schmidt, Claudia; Izbicki, Jakob R.; Holscher, Arnulf H.; Lang, Hauke; Lorenz, Dietmar; Schumacher, Brigitte; Mayershofer, Rupert; Vashist, Yogesh; Ott, Katja; Vieth, Michael; Weismueller, Josef; Nothen, Markus M.; Moebus, Susanne; Knapp, Michael; Peters, Wilbert H. M.; Neuhaus, Horst; Rosch, Thomas; Ell, Christian; Jankowski, Janusz; Schumacher, Johannes; Neale, Rachel E.; Whiteman, David C.; Thrift, Aaron P.
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Genetic testing in patients with retinitis pigmentosa: Features of unsolved cases
err2019-05-08
err12
errOAAI
errBirtel, Johannes; Gliem, Martin; Oishi, Akio; Mueller, Philipp L.; Herrmann, Philipp; Holz, Frank G.; Mangold, Elisabeth; Knapp, Michael; Bolz, Hanno J.; Issa, Peter Charbel
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p63 establishes epithelial enhancers at critical craniofacial development genes
err2019-05-03
err40
errOAAI
errLin-Shiao, Enrique; Lan, Yemin; Welzenbach, Julia; Alexander, Katherine A.; Zhang, Zhen; Knapp, Michael; Mangold, Elisabeth; Sammons, Morgan; Ludwig, Kerstin U.; Berger, Shelley L.
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First genotype-phenotype study reveals HLA-DQβ1 insertion heterogeneity in high-resolution manometry achalasia subtypes
err2019-02-01
err9
errOAAI
errVackova, Zuzana; Niebisch, Stefan; Triantafyllou, Tania; Becker, Jessica; Hess, Timo; Kreuser, Nicole; Kanoni, Stavroula; Deloukas, Panos; Schueller, Vitalia; Heinrichs, Sophie K. M.; Thieme, Rene; Noethen, Markus M.; Knapp, Michael; Spicak, Julius; Gockel, Ines; Schumacher, Johannes; Theodorou, Dimitris; Martinek, Jan
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Evidence for DNA methylation mediating genetic liability to non-syndromic cleft lip/palateDNA甲基化介导非综合征性唇腭裂遗传易感性的证据
err2019-01-14
err24
errOAAI
errHowe, Laurence J.; Richardson, Tom G.; Arathimos, Ryan; Alvizi, Lucas; Passos-Bueno, Maria R.; Stanier, Philip; Nohr, Ellen; Ludwig, Kerstin U.; Mangold, Elisabeth; Knapp, Michael; Stergiakouli, Evie; St Pourcain, Beate; Smith, George Davey; Sandy, Jonathan; Relton, Caroline L.; Lewis, Sarah J.; Hemani, Gibran; Sharp, Gemma C.
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Premorbid adjustment and schizophrenia
err2018-01-03
err2
PREAI
errKrauss, H; Knapp, M; Schulze, T; Rietschel, M
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