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M

M. Litt

University of Pennsylvania Perelman School of Medicine

49H指数
209论文数
9.0K被引数
收录论文 27
发表时间
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Left Bundle Branch Area Pacing in Patients With Cardiac Sarcoidosis心脏结节病患者中的左束支区域起搏
errJACC: Clinical Electrophysiology
IF0
err2025-11-20
err0
PREAI
errMichael Gurin; Michael Litt; Tarek Zghaib; Carli Peters; Timothy M. Markman; Jeffrey J. Luebbert; Michael P. Riley; Poojita Shivamurthy; Matthew C. Hyman; Rajat Deo; Gustavo S. Guandalini; Saman Nazarian; Gregory E. Supple; David S. Frankel; Francis E. Marchlinski; Robert D. Schaller
err分享
err收藏
Para-Hisian Ventricular Arrhythmias: Insights from Septal Coronary Venous Mapping间隔旁室性心律失常：间隔冠状静脉标测的见解
errHeart Rhythm
IF5.7
err2025-11-06
err0
PREAI
errAndres Enriquez; Jose Angel Cabrera; Damian Sanchez-Quintana; Tarek Zghaib; Michael Litt; Mohamed Gad; Timothy Markman; David S. Frankel; Francis Marchlinski; Fermin Garcia
err分享
err收藏
Histone deacetylase 6 inhibition restores leptin sensitivity and reduces obesity
errNATURE METABOLISM
IF20.8
err2022-01-17
err35
errOAAI
errCakir, Ism; Hadley, Colleen K.; Pan, Pauline Lining; Bagchi, Rushita A.; Ghamari-Langroudi, Masoud; Porter, Danielle T.; Wang, Qiuyu; Litt, Michael J.; Jana, Somnath; Hagen, Susan; Lee, Pil; White, Andrew; Lin, Jiandie D.; McKinsey, Timothy A.; Cone, Roger D.
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err收藏
Hard to Swallow
errNEW ENGLAND JOURNAL OF MEDICINE
IF78.5
err2021-10-07
err2
PREAI
errLitt, Michael J.; Montgomery, Mary W.; Small, Kirstin M.; Miller, Amy L.; Loscalzo, Joseph
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err收藏
Cardiac Phenotype and Tissue Sodium Content in Adolescents With Defects in the Melanocortin System
errJOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
IF5.1
err2021-05-24
err3
errOAAI
errPuder, Lia; Roth, Sophie; Krabusch, Philipp; Wiegand, Susanna; Opitz, Robert; Bald, Martin; Flueck, Christa; Schulz, Esther; Voss, Egbert; Marko, Lajos; Linz, Peter; Berger, Felix; Muller, Dominik N.; Kuehne, Titus; Litt, Michael J.; Cone, Roger D.; Kuehnen, Peter; Kelm, Marcus
err分享
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Late onset obesity in mice with targeted deletion of potassium inward rectifier Kir7.1 from cells expressing the melanocortin-4 receptor
errJOURNAL OF NEUROENDOCRINOLOGY
IF4.1
err2019-01-20
err19
errOAAI
errAnderson, Erica J. P.; Ghamari-Langroudi, Masoud; Cakir, Isin; Litt, Michael J.; Chen, Valerie; Reggiardo, Roman E.; Millhauser, Glenn L.; Cone, Roger D.
err分享
err收藏
Regulation of energy rheostasis by the melanocortin-3 receptor
errSCIENCE ADVANCES
IF12.5
err2018-08-03
err43
errOAAI
errGhamari-Langroudi, Masoud; Cakir, Isin; Lippert, Rachel N.; Sweeney, Patrick; Litt, Michael J.; Ellacott, Kate L. J.; Cone, Roger D.
err分享
err收藏
Loss of the melanocortin-4 receptor in mice causes dilated cardiomyopathy
errELIFE
IF0
err2017-08-22
err16
errOAAI
errLitt, Michael J.; Okoye, G. Donald; Lark, Daniel; Cakir, Isin; Moore, Christy; Barber, Mary C.; Atkinson, James; Fessel, Josh; Moslehi, Javid; Cone, Roger D.
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err收藏
Regulation of feeding and energy homeostasis by α-MSH
errJOURNAL OF MOLECULAR ENDOCRINOLOGY
IF3.8
err2016-05-01
err145
errOAAI
errAnderson, Erica J. P.; Cakir, Isin; Carrington, Sheridan J.; Cone, Roger D.; Ghamari-Langroudi, Masoud; Gillyard, Taneisha; Gimenez, Luis E.; Litt, Michael J.
err分享
err收藏
DMH1, a Highly Selective Small Molecule BMP Inhibitor Promotes Neurogenesis of hiPSCs: Comparison of PAX6 and SOX1 Expression during Neural Induction
errACS CHEMICAL NEUROSCIENCE
IF3.9
err2012-03-15
err112
errOAAI
errNeely, M. Diana; Litt, Michael J.; Tidball, Andrew M.; Li, Gary G.; Aboud, Asad A.; Hopkins, Corey R.; Chamberlin, Reed; Hong, Charles C.; Ess, Kevin C.; Bowman, Aaron B.
err分享
err收藏
Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy
errAMERICAN HEART JOURNAL
IF3.5
err2008-07-01
err197
errOAAI
errParks, Sharie B.; Kushner, Jessica D.; Nauman, Deirdre; Burgess, Donna; Ludwigsen, Susan; Peterson, Amanda; Li, Duanxiang; Jakobs, Petra; Litt, Michael; Porter, Charles B.; Rahko, Peter S.; Hershberger, Ray E.
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err收藏
Coding Sequence Mutations Identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 Patients with Familial or Idiopathic Dilated Cardiomyopathy
errCTS-CLINICAL AND TRANSLATIONAL SCIENCE
IF2.8
err2008-05-21
err177
errOAAI
errHershberger, Ray E.; Parks, Sharie B.; Kushner, Jessica D.; Li, Duanxiang; Ludwigsen, Susan; Jakobs, Petra; Nauman, Deirdre; Burgess, Donna; Partain, Julie; Litt, Michael
err分享
err收藏
Mutations of presenilin genes in dilated cardiomyopathy and heart failure
errAMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
err2006-12-01
err164
errOAAI
errLi, Duanxiang; Parks, Sharie B.; Kushner, Jessica D.; Nauman, Deirdre; Burgess, Donna; Ludwigsen, Susan; Partain, Julie; Nixon, Randal R.; Allen, Charles N.; Irwin, Robert P.; Jakobs, Petra M.; Litt, Michael; Hershberger, Ray E.
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Modulation of the age at onset of Parkinson's disease by apolipoprotein E genotypes
errANNALS OF NEUROLOGY
IF7.7
err2004-10-08
err51
PREAI
errZareparsi, S; Kaye, J; Camicioli, R; Grimslid, H; Oken, B; Litt, M; Nutt, J; Bird, T; Schellenberg, G; Payami, H
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err收藏
A novel lamin A/C mutation in a family with dilated cardiomyopathy, prominent conduction system disease, and need for permanent pacemaker implantation
errAMERICAN HEART JOURNAL
IF3.5
err2002-12-01
err52
PREAI
errHershberger, RE; Hanson, EL; Jakobs, PM; Keegan, H; Coates, K; Bousman, S; Litt, M
err分享
err收藏
Cardiac troponin T lysine 210 deletion in a family with dilated cardiomyopathy
errJOURNAL OF CARDIAC FAILURE
IF8.2
err2002-02-01
err60
PREAI
errHanson, EL; Jakobs, PM; Keegan, H; Coates, K; Bousman, S; Dienel, NH; Litt, M; Hershberger, RE
err分享
err收藏
Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease
errJOURNAL OF CARDIAC FAILURE
IF8.2
err2001-09-01
err99
PREAI
errJakobs, PM; Hanson, EL; Crispell, KA; Toy, W; Keegan, H; Schilling, K; Icenogle, TB; Litt, M; Hershberger, RE
err分享
err收藏
Paroxysmal kinesigenic dyskinesia and infantile convulsions -: Clinical and linkage studies
errNEUROLOGY
IF8.5
err2000-07-25
err107
PREAI
errSwoboda, KJ; Soong, BW; McKenna, C; Brunt, ERP; Litt, M; Bale, JF; Ashizawa, T; Bennett, LB; Bowcock, AM; Roach, ES; Gerson, D; Matsuura, T; Heydemann, PT; Nespeca, MP; Jankovic, J; Leppert, M; Ptácek, LJ
err分享
err收藏
Autosomal-dominant congenital cataract associated with a deletion mutation in the human beaded filament protein gene BFSP2
errAMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
err2000-04-01
err164
errOAAI
errJakobs, PM; Hess, JF; FitzGerald, PG; Kramer, P; Weleber, RG; Litt, M
err分享
err收藏
A novel nonsense mutation in CACNA1A causes episodic ataxia and hemiplegiaCACNA1A中的一种新的无义突变导致发作性共济失调和偏瘫
errNEUROLOGY
IF8.5
err1999-07-01
err101
PREAI
errJen, J; Yue, Q; Nelson, SF; Yu, H; Litt, M; Nutt, J; Baloh, RW
err分享
err收藏

研究方向

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