Marie E. Faughnan - Publications, H-index & Citations

Marie E. Faughnan

pennsylvania medicine

42H指数

177论文数

8.3K被引数

收录论文 80

发表时间

The Untitled 无标题

EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY

IF2.2

2025-11-01

PREAI

Iyer, 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

Assessing racial differences in North American hereditary hemorrhagic telangiectasia study recruitment and care 评估北美遗传性出血性毛细血管扩张症研究中种族差异的招募与护理

Orphanet Journal of Rare Diseases

IF3.5

2025-08-29

OAAI

Gabriella Scott; Ashlee Agundiz; Jeffrey Nelson; Steven Hetts; Marianne Clancy; Helen Kim; Marie E. Faughnan

Standardization of Terminology, Definitions, and Outcome Criteria for Bleeding in Hereditary Hemorrhagic Telangiectasia: International Consensus Report 遗传性出血性毛细血管扩张症出血的术语、定义和结局标准标准化：国际共识报告

American Journal of Hematology

IF9.9

2025-07-15

OAAI

Hanny 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

Somatic mutations in arteriovenous malformations in hereditary hemorrhagic telangiectasia support a bi-allelic two-hit mutation mechanism of pathogenesis (vol 111, pg 2283, 2024)遗传性出血性毛细血管扩张症动静脉畸形的体细胞突变支持双等位基因两击突变的发病机制 (111卷，2283页，2024页)

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2025-04-01

PREAI

DeBose-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.

Health outcomes following COVID-19 infection and vaccination in hereditary hemorrhagic telangiectasia

ORPHANET JOURNAL OF RARE DISEASES

IF3.5

2025-03-01

OAAI

Tarulli, Christopher M.; Ma, Xiayi; Chokar, Kamalprit; Vozoris, Nicholas T.; Clancy, Marianne S.; Faughnan, Marie E.

Brain and lung arteriovenous malformation rescreening practices for children and adults with hereditary hemorrhagic telangiectasia

ORPHANET JOURNAL OF RARE DISEASES

IF3.5

2024-11-09

OAAI

Beslow, Lauren A.; Kim, Helen; Hetts, Steven W.; Ratjen, Felix; Clancy, Marianne S.; Gossage, James R.; Faughnan, Marie E.

CDK6-mediated endothelial cell cycle acceleration drives arteriovenous malformations in hereditary hemorrhagic telangiectasia

cardiovascular research

IF10.8

2024-11-01

PREAI

Dinakaran, 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

Somatic mutations in arteriovenous malformations in hereditary hemorrhagic telangiectasia support a bi-allelic two-hit mutation mechanism of pathogenesis

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2024-10-01

PREAI

De Novo Brain Vascular Malformations in Hereditary Hemorrhagic Telangiectasia 遗传性出血性毛细血管扩张症的新生脑血管畸形

PEDIATRIC NEUROLOGY

IF2.1

2024-06-01

PREAI

Beslow, 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.

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 回复Eker等人。评论Kilian等人。比较HHT儿童和成人脑血管畸形的特征和治疗。J.Clin.医学。2023，12，2704

JOURNAL OF CLINICAL MEDICINE

IF2.9

2023-12-01

OAAI

Kilian, 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.

Prevalence and Characteristics of Intracranial Aneurysms in Hereditary Hemorrhagic Telangiectasia

AMERICAN JOURNAL OF NEURORADIOLOGY

IF3.7

2023-11-30

PREAI

Cheng, How-Chung; Faughnan, Marie E.; terBrugge, Karel G.; Liu, Hon-Man; Krings, Timo

Comparing Characteristics and Treatment of Brain Vascular Malformations in Children and Adults with HHT

JOURNAL OF CLINICAL MEDICINE

IF2.9

2023-04-04

OAAI

Kilian, 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

Randomized, double-blind, placebo-controlled, crossover trial of oral doxycycline for epistaxis in hereditary hemorrhagic telangiectasia

ORPHANET JOURNAL OF RARE DISEASES

IF3.5

2022-11-07

OAAI

Thompson, K. P.; Sykes, J.; Chandakkar, P.; Marambaud, P.; Vozoris, N. T.; Marchuk, D. A.; Faughnan, M. E.

Quantification metrics for telangiectasia using optical coherence tomography

SCIENTIFIC REPORTS

IF3.9

2022-02-02

OAAI

Cardinell, 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.

Utility of modified Rankin Scale for brain vascular malformations in hereditary hemorrhagic telangiectasia

ORPHANET JOURNAL OF RARE DISEASES

IF3.5

2021-09-19

OAAI

Thompson, K. P.; Nelson, J.; Kim, H.; Weinsheimer, S. M.; Marchuk, D. A.; Lawton, M. T.; Krings, T.; Faughnan, M. E.

Pilot investigation of circulating angiogenic and inflammatory biomarkers associated with vascular malformations

ORPHANET JOURNAL OF RARE DISEASES

IF3.5

2021-09-03

OAAI

Wetzel-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.

Endoglin deficiency impairs VEGFR2 but not FGFR1 or TIE2 activation and alters VEGF-mediated cellular responses in human primary endothelial cells

TRANSLATIONAL RESEARCH

IF5.9

2021-09-01

OAAI

Zhang, Qiuwang; Wang, Chenxi; Cannavicci, Anthony; Faughnan, Marie E.; Kutryk, Michael J. B.

Second International Guidelines for the Diagnosis and Management of Hereditary Hemorrhagic Telangiectasia RESPONSE

ANNALS OF INTERNAL MEDICINE

IF15.2

2021-07-01

PREAI

Faughnan, Marie E.; Mager, Johannes J.; Hetts, Steven W.; Palda, Valerie A.; Ratjen, Felix

Circulating Plasma Biomarkers Associated With Brain Arteriovenous Malformations.

STROKE

IF8.9

2021-03-01

PREAI

Wetzel-Strong, Sarah E.; Weinsheimer, Shantel M.; Nelson, Jeffrey; Pawlikowska, Ludmila; Clark, Dewi; McCulloch, Charles E.; Kim, Helen; Faughnan, Marie E.; Marchuk, Douglas A.

Predictors of mortality in patients with hereditary hemorrhagic telangiectasia 遗传性出血性毛细血管扩张症患者死亡率的预测因素

ORPHANET JOURNAL OF RARE DISEASES

IF3.5

2021-01-06

OAAI

Thompson, K. P.; Nelson, J.; Kim, H.; Pawlikowska, L.; Marchuk, D. A.; Lawton, M. T.; Faughnan, Marie E.

研究方向