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M

Marie E. Faughnan

pennsylvania medicine

42H-index
177Paper Count
8.3KCitation Count
Published Papers 80
Publication Date
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The Untitled
errEUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY
IF2.2
err2025-11-01
err0
PREAI
errIyer, Vivek N.; Vethanayagam, Dilini; Al-Samkari, Hanny; Beslow, Lauren A.; Chakinala, Murali; Decker, Jake E.; Faughnan, Marie E.; Galiatsatos, Panagis; Gane, Simon; Geisthoff, Urban; Gossage, James R.; De Gussem, Els; Hammill, Adrienne M.; Kasthuri, Raj; Rodriguez-Lopez, Josanna; Mcwilliams, Justin; Mei-Zahav, Meir; Muralidhar, Akshay; Pishko, Allyson; Olitsky, Scott E.; Pollak, Jeffrey S.; Pynnonen, Melissa A.; Semple, Malcolm G.; Sukumar, Senthil; Tobis, Jonathan; Trerotola, Scott O.; Weiss, Clifford R.; White, Andrew J.; Zhou, Jenny; Friday, Cassi; Clancy, Marianne
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Assessing racial differences in North American hereditary hemorrhagic telangiectasia study recruitment and care
errOrphanet Journal of Rare Diseases
IF3.5
err2025-08-29
err0
errOAAI
errGabriella Scott; Ashlee Agundiz; Jeffrey Nelson; Steven Hetts; Marianne Clancy; Helen Kim; Marie E. Faughnan
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Standardization of Terminology, Definitions, and Outcome Criteria for Bleeding in Hereditary Hemorrhagic Telangiectasia: International Consensus Report
errAmerican Journal of Hematology
IF9.9
err2025-07-15
err0
errOAAI
errHanny Al-Samkari; Raj S. Kasthuri; Hans-Jurgen Mager; Jenny Y. Zhou; Marcelo M. Serra; Bethany T. Samuelson-Bannow; Layla N. Van Doren; Jay F. Piccirillo; Marianne S. Clancy; Keith R. McCrae; Sonia M. Thomas; Antoni Riera-Mestre; Allyson M. Pishko; Sarah Sewaralthahab; James R. Gossage; Vivek N. Iyer; Cedric Hermans; Adrienne Hammill; Ingrid Winship; Meir Mei-Zahav; Annette von Drygalski; Scott Olitsky; Marie E. Faughnan
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errSave
Somatic mutations in arteriovenous malformations in hereditary hemorrhagic telangiectasia support a bi-allelic two-hit mutation mechanism of pathogenesis (vol 111, pg 2283, 2024)
errAMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
err2025-04-01
err0
PREAI
errDeBose-Scarlett, Evon; Ressler, Andrew K.; Gallione, Carol J.; Cantis, Gonzalo Sapisochin; Friday, Cassi; Weinsheimer, Shantel; Schimmel, Katharina; Spiekerkoetter, Edda; Kim, Helen; Gossage, James R.; Faughnan, Marie E.; Marchuk, Douglas A.
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errSave
Health outcomes following COVID-19 infection and vaccination in hereditary hemorrhagic telangiectasia
errORPHANET JOURNAL OF RARE DISEASES
IF3.5
err2025-03-01
err0
errOAAI
errTarulli, Christopher M.; Ma, Xiayi; Chokar, Kamalprit; Vozoris, Nicholas T.; Clancy, Marianne S.; Faughnan, Marie E.
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errSave
Brain and lung arteriovenous malformation rescreening practices for children and adults with hereditary hemorrhagic telangiectasia
errORPHANET JOURNAL OF RARE DISEASES
IF3.5
err2024-11-09
err0
errOAAI
errBeslow, Lauren A.; Kim, Helen; Hetts, Steven W.; Ratjen, Felix; Clancy, Marianne S.; Gossage, James R.; Faughnan, Marie E.
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errSave
CDK6-mediated endothelial cell cycle acceleration drives arteriovenous malformations in hereditary hemorrhagic telangiectasia
errcardiovascular research
IF10.8
err2024-11-01
err1
PREAI
errDinakaran, Sajeth; Qutaina, Sima; Zhao, Haitian; Tang, Yuefeng; Wang, Zhimin; Ruiz, Santiago; Nomura-Kitabayashi, Aya; Metz, Christine N.; Arthur, Helen M.; Meadows, Stryder M.; Blanc, Lionel; Faughnan, Marie E.; Marambaud, Philippe
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errSave
Somatic mutations in arteriovenous malformations in hereditary hemorrhagic telangiectasia support a bi-allelic two-hit mutation mechanism of pathogenesis
errAMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
err2024-10-01
err2
PREAI
errDeBose-Scarlett, Evon; Ressler, Andrew K.; Gallione, Carol J.; Cantis, Gonzalo Sapisochin; Friday, Cassi; Weinsheimer, Shantel; Schimmel, Katharina; Spiekerkoetter, Edda; Kim, Helen; Gossage, James R.; Faughnan, Marie E.; Marchuk, Douglas A.
errShare
errSave
De Novo Brain Vascular Malformations in Hereditary Hemorrhagic Telangiectasia
errPEDIATRIC NEUROLOGY
IF2.1
err2024-06-01
err4
PREAI
errBeslow, Lauren A.; Krings, Timo; Kim, Helen; Hetts, Steven W.; Lawton, Michael T.; Ratjen, Felix; Whitehead, Kevin J.; Gossage, James R.; McCulloch, Charles E.; Clancy, Marianne; Bagheri, Negar; Faughnan, Marie E.
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Reply to Eker et al. Comment on Kilian et al. Comparing Characteristics and Treatment of Brain Vascular Malformations in Children and Adults with HHT. J. Clin. Med. 2023, 12, 2704
errJOURNAL OF CLINICAL MEDICINE
IF2.9
err2023-12-01
err0
errOAAI
errKilian, Alexandra; Latino, Giuseppe A.; White, Andrew J.; Ratjen, Felix; McDonald, Jamie; Whitehead, Kevin J.; Gossage, James R.; Krings, Timo; Lawton, Michael T.; Kim, Helen; Faughnan, Marie E.
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errSave
Prevalence and Characteristics of Intracranial Aneurysms in Hereditary Hemorrhagic Telangiectasia
errAMERICAN JOURNAL OF NEURORADIOLOGY
IF3.7
err2023-11-30
err1
PREAI
errCheng, How-Chung; Faughnan, Marie E.; terBrugge, Karel G.; Liu, Hon-Man; Krings, Timo
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errSave
Comparing Characteristics and Treatment of Brain Vascular Malformations in Children and Adults with HHT
errJOURNAL OF CLINICAL MEDICINE
IF2.9
err2023-04-04
err10
errOAAI
errKilian, Alexandra A.; Latino, Giuseppe J.; White, Andrew; Ratjen, Felix; McDonald, Jamie J.; Whitehead, Kevin R.; Gossage, James; Krings, Timo T.; Lawton, Michael; Kim, Helen E.; Faughnan, Marie
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errSave
Randomized, double-blind, placebo-controlled, crossover trial of oral doxycycline for epistaxis in hereditary hemorrhagic telangiectasia
errORPHANET JOURNAL OF RARE DISEASES
IF3.5
err2022-11-07
err9
errOAAI
errThompson, K. P.; Sykes, J.; Chandakkar, P.; Marambaud, P.; Vozoris, N. T.; Marchuk, D. A.; Faughnan, M. E.
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errSave
Quantification metrics for telangiectasia using optical coherence tomography
errSCIENTIFIC REPORTS
IF3.9
err2022-02-02
err0
errOAAI
errCardinell, Jillian L.; Ramjist, Joel M.; Chen, Chaoliang; Shi, Weisong; Nguyen, Nhu Q.; Yeretsian, Tiffany; Choi, Matthew; Chen, David; Clark, Dewi S.; Curtis, Anne; Kim, Helen; Faughnan, Marie E.; Yang, Victor X. D.
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Utility of modified Rankin Scale for brain vascular malformations in hereditary hemorrhagic telangiectasia
errORPHANET JOURNAL OF RARE DISEASES
IF3.5
err2021-09-19
err1
errOAAI
errThompson, K. P.; Nelson, J.; Kim, H.; Weinsheimer, S. M.; Marchuk, D. A.; Lawton, M. T.; Krings, T.; Faughnan, M. E.
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Pilot investigation of circulating angiogenic and inflammatory biomarkers associated with vascular malformations
errORPHANET JOURNAL OF RARE DISEASES
IF3.5
err2021-09-03
err12
errOAAI
errWetzel-Strong, Sarah E.; Weinsheimer, Shantel; Nelson, Jeffrey; Pawlikowska, Ludmila; Clark, Dewi; Starr, Mark D.; Liu, Yingmiao; Kim, Helen; Faughnan, Marie E.; Nixon, Andrew B.; Marchuk, Douglas A.
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errSave
Endoglin deficiency impairs VEGFR2 but not FGFR1 or TIE2 activation and alters VEGF-mediated cellular responses in human primary endothelial cells
errTRANSLATIONAL RESEARCH
IF5.9
err2021-09-01
err7
errOAAI
errZhang, Qiuwang; Wang, Chenxi; Cannavicci, Anthony; Faughnan, Marie E.; Kutryk, Michael J. B.
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errSave
Second International Guidelines for the Diagnosis and Management of Hereditary Hemorrhagic Telangiectasia RESPONSE
errANNALS OF INTERNAL MEDICINE
IF15.2
err2021-07-01
err18
PREAI
errFaughnan, Marie E.; Mager, Johannes J.; Hetts, Steven W.; Palda, Valerie A.; Ratjen, Felix
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errSave
Circulating Plasma Biomarkers Associated With Brain Arteriovenous Malformations.
errSTROKE
IF8.9
err2021-03-01
err0
PREAI
errWetzel-Strong, Sarah E.; Weinsheimer, Shantel M.; Nelson, Jeffrey; Pawlikowska, Ludmila; Clark, Dewi; McCulloch, Charles E.; Kim, Helen; Faughnan, Marie E.; Marchuk, Douglas A.
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errSave
Predictors of mortality in patients with hereditary hemorrhagic telangiectasia
errORPHANET JOURNAL OF RARE DISEASES
IF3.5
err2021-01-06
err17
errOAAI
errThompson, K. P.; Nelson, J.; Kim, H.; Pawlikowska, L.; Marchuk, D. A.; Lawton, M. T.; Faughnan, Marie E.
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errSave

Research Directions

No research directions
Co-authors
Cooperation Journals
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Steven Gallinger
H-index: 122 · Papers: 1.4K
C
Charles E. McCulloch
H-index: 115 · Papers: 1.1K
V
Vincent Cottin
H-index: 108 · Papers: 1.4K
G
George Tomlinson
H-index: 107 · Papers: 864
G
Guadalupe García–Tsao
H-index: 102 · Papers: 495
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