logo
科言猫学术研究的AI总结
language
手机端手机端
  • Phone Feature微信小程序
简体中文简体中文
notice消息通知
博客博客
arrow
S

Steven R. DePalma

Harvard University
H指数:35
被引数:9,313

个人简介

暂无内容

教育背景

暂无内容

工作经历

暂无内容

荣誉奖项

暂无内容

Modeling SMAD2 Mutations in Induced Pluripotent Stem Cells Provides Insights Into Cardiovascular Disease Pathogenesis

模拟诱导多能干细胞中的SMAD2突变提供了对心血管疾病发病机理的见解

JOURNAL OF THE AMERICAN HEART ASSOCIATION
IF5.3
2025-03-040
PRE
Ward, Tarsha; Morton, Sarah U.; Venturini, Gabriela; Tai, Warren; Jang, Min Young; Gorham, Joshua; Delaughter, Dan; Wasson, Lauren K.; Khazal, Zahra; Homsy, Jason; Gelb, Bruce D.; Chung, Wendy K.; Bruneau, Benoit G.; Brueckner, Martina; Tristani-Firouzi, Martin; Depalma, Steven R.; Seidman, Christine; Seidman, J. G.
Noncoding variants and sulcal patterns in congenital heart disease: Machine learning to predict functional impact

非编码变异和脑沟模式在先天性心脏病中的作用：机器学习预测功能影响

ISCIENCE
IF4.1
2025-02-011
OAAI
Mondragon-Estrada, Enrique; Newburger, Jane W.; Depalma, Steven R.; Brueckner, Martina; Cleveland, John; Chung, Wendy K.; Gelb, Bruce D.; Goldmuntz, Elizabeth; Hagler Jr, Donald J.; Mcquillen, Patrick; Miller, Thomas A.; Panigrahy, Ashok; Porter Jr, George A.; Roberts, Amy E.; Rollins, Caitlin K.; Russell, Mark W.; Tristani-Firouzi, Martin; Grant, P. Ellen; Im, Kiho; Morton, Sarah U.
Increased endothelial sclerostin caused by elevated DSCAM mediates multiple trisomy 21 phenotypes
JOURNAL OF CLINICAL INVESTIGATION
IF13.6
2024-06-030
OAAI
Mckean, David M.; Zhang, Qi; Narayan, Priyanka; Morton, Sarah U.; Strohmenger, Viktoria; Tang, Vi T.; Mcallister, Sophie; Sharma, Ananya; Quiat, Daniel; Reichart, Daniel; Delaughter, Daniel M.; Wakimoto, Hiroko; Gorham, Joshua M.; Brown, Kemar; Mcdonough, Barbara; Willcox, Jon A.; Jang, Min Young; Depalma, Steven R.; Ward, Tarsha; Investigators, Pediatric Cardiac Genomics Consortium; Kim, Richard; Cleveland, John D.; Seidman, J. G.; Seidman, Christine E.
Contribution of Previously Unrecognized RNA Splice-Altering Variants to Congenital Heart Disease
CIRCULATION-GENOMIC AND PRECISION MEDICINE
IF5.5
2023-06-014
OA
Jang, Min Young; Patel, Parth N.; Pereira, Alexandre C.; Willcox, Jon A. L.; Haghighi, Alireza; Tai, Angela C.; Ito, Kaoru; Morton, Sarah U.; Gorham, Joshua M.; McKean, David M.; DePalma, Steven R.; Bernstein, Daniel; Brueckner, Martina; Chung, Wendy K.; Giardini, Alessandro; Goldmuntz, Elizabeth; Kaltman, Jonathan R.; Kim, Richard; Newburger, Jane W.; Shen, Yufeng; Srivastava, Deepak; Tristani-Firouzi, Martin; Gelb, Bruce D.; Porter, Jr George A.; Seidman, Christine E.; Seidman, Jonathan G.
Damaging variants in FOXI3 cause microtia and craniofacial microsomia
GENETICS IN MEDICINE
IF6.2
2023-01-0111
OAAI
Quiat, Daniel; Timberlake, Andrew T.; Curran, Justin J.; Cunningham, Michael L.; McDonough, Barbara; Artunduaga, Maria A.; DePalma, Steven R.; Duenas-Roque, Milagros M.; Gorham, Joshua M.; Gustafson, Jonas A.; Hamdan, Usama; V. Hing, Anne; Hurtado-Villa, Paula; Nicolau, Yamileth; Osorno, Gabriel; Pachajoa, Harry; Porras-Hurtado, Gloria L.; Quintanilla-Dieck, Lourdes; Serrano, Luis; Tumblin, Melissa; Zarante, Ignacio; V. Luquetti, Daniela; Eavey, Roland D.; Heike, Carrie L.; Seidman, Jonathan G.; Seidman, Christine E.
An ancient founder mutation located between ROBO1 and ROBO2 is responsible for increased microtia risk in Amerindigenous populations
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
IF9.1
2022-05-186
OAAI
Quiat, Daniel; Kim, Seong Won; Zhang, Qi; Morton, Sarah U.; Pereira, Alexandre C.; DePalma, Steven R.; Willcox, Jon A. L.; McDonough, Barbara; DeLaughter, Daniel M.; Gorham, Joshua M.; Curran, Justin J.; Tumblin, Melissa; Nicolau, Yamileth; Artunduaga, Maria A.; Quintanilla-Dieck, Lourdes; Osorno, Gabriel; Serrano, Luis; Hamdan, Usama; Eavey, Roland D.; Seidman, Christine E.; Seidman, J. G.
Neither cardiac mitochondrial DNA variation nor copy number contribute to congenital heart disease risk
AMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
2022-05-017
OAAI
Willcox, Jon A. L.; Geiger, Joshua T.; Morton, Sarah U.; McKean, David; Quiat, Daniel; Gorham, Joshua M.; Tai, Angela C.; DePalma, Steven; Bernstein, Daniel; Brueckner, Martina; Chung, Wendy K.; Giardini, Alessandro; Goldmuntz, Elizabeth; Kaltman, Jonathan R.; Kim, Richard; Newburger, Jane W.; Shen, Yufeng; Srivastava, Deepak; Tristani-Firouzi, Martin; Gelb, Bruce; Porter, George A., Jr.; Seidman, J. G.; Seidman, Christine E.
Genetic and Phenotypic Landscape of Peripartum Cardiomyopathy

围产期心肌病的遗传和表型景观

CIRCULATION
IF38.6
2021-05-1187
OA
Goli, Rahul; Li, Jian; Brandimarto, Jeff; Levine, Lisa D.; Riis, Valerie; McAfee, Quentin; DePalma, Steven; Haghighi, Alireza; Seidman, J. G.; Seidman, Christine E.; Jacoby, Daniel; Macones, George; Judge, Daniel P.; Rana, Sarosh; Margulies, Kenneth B.; Cappola, Thomas P.; Alharethi, Rami; Damp, Julie; Hsich, Eileen; Elkayam, Uri; Sheppard, Richard; Alexis, Jeffrey D.; Boehmer, John; Kamiya, Chizuko; Gustafsson, Finn; Damm, Peter; Ersboll, Anne S.; Goland, Sorel; Hilfiker-Kleiner, Denise; McNamara, Dennis M.; Arany, Zolt
Mechanisms of Congenital Heart Disease Caused by NAA15 Haploinsufficiency
CIRCULATION RESEARCH
IF16.2
2021-04-1624
OAAI
Ward, Tarsha; Tai, Warren; Morton, Sarah; Impens, Francis; Van Damme, Petra; Van Haver, Delphi; Timmerman, Evy; Venturini, Gabriela; Zhang, Kehan; Jang, Min Young; Willcox, Jon A. L.; Haghighi, Alireza; Gelb, Bruce D.; Chung, Wendy K.; Goldmuntz, Elizabeth; Porter, George A., Jr.; Lifton, Richard P.; Brueckner, Martina; Yost, H. Joseph; Bruneau, Benoit G.; Gorham, Joshua; Kim, Yuri; Pereira, Alexandre; Homsy, Jason; Benson, Craig C.; DePalma, Steven R.; Varland, Sylvia; Chen, Christopher S.; Arnesen, Thomas; Gevaert, Kris; Seidman, Christine; Seidman, J. G.
Rare genetic variation at transcription factor binding sites modulates local DNA methylation profiles
PLOS GENETICS
IF3.7
2020-11-2023
OAAI
Martin-Trujillo, Alejandro; Patel, Nihir; Richter, Felix; Jadhav, Bharati; Garg, Paras; Morton, Sarah U.; McKean, David M.; DePalma, Steven R.; Goldmuntz, Elizabeth; Gruber, Dorota; Kim, Richard; Newburger, Jane W.; Porter, George A., Jr.; Giardini, Alessandro; Bernstein, Daniel; Tristani-Firouzi, Martin; Seidman, Jonathan G.; Seidman, Christine E.; Chung, Wendy K.; Gelb, Bruce D.; Sharp, Andrew J.
GATA6 mutations in hiPSCs inform mechanisms for maldevelopment of the heart, pancreas, and diaphragm
ELIFE
IF0
2020-10-1540
OA
Sharma, Arun; Wasson, Lauren K.; Al Willcox, Jon; Morton, Sarah U.; Gorham, Joshua M.; DeLaughter, Daniel M.; Neyazi, Meraj; Schmid, Manuel; Agarwal, Radhika; Jang, Min Young; Toepfer, Christopher N.; Ward, Tarsha; Kim, Yuri; Pereira, Alexandre C.; DePalma, Steven R.; Tai, Angela; Kim, Seongwon; Conner, David; Bernstein, Daniel; Gelb, Bruce D.; Chung, Wendy K.; Goldmuntz, Elizabeth; Porter, George; Tristani-Firouzi, Martin; Srivastava, Deepak; Seidman, Jonathan G.; Seidman, Christine E.
Genomic analyses implicate noncoding de novo variants in congenital heart disease

基因组分析暗示先天性心脏病中的非编码从头变异

NATURE GENETICS
IF31.8
2020-06-29100
OAAI
Richter, Felix; Morton, Sarah U.; Kim, Seong Won; Kitaygorodsky, Alexander; Wasson, Lauren K.; Chen, Kathleen M.; Zhou, Jian; Qi, Hongjian J.; Patel, Nihir; DePalma, Steven R.; Parfenov, Michael; Homsy, Jason; Gorham, Joshua M.; Manheimer, Kathryn B.; Velinder, Matthew; Farrell, Andrew; Marth, Gabor; Schadt, Eric E.; Kaltman, Jonathan R.; Newburger, Jane W.; Giardini, Alessandro; Goldmuntz, Elizabeth; Brueckner, Martina; Kim, Richard; Porter, George A., Jr.; Bernstein, Daniel; Chung, Wendy K.; Srivastava, Deepak; Tristani-Firouzi, Martin; Troyanskaya, Olga G.; Dickel, Diane E.; Shen, Yufeng; Seidman, Jonathan G.; Seidman, Christine E.; Gelb, Bruce D.

研究方向

暂未获取到该数据
C
Christine E. Seidman
H 指数:151论文数:713被引数:9.0万
J
Jonathan G. Seidman
H 指数:132论文数:536被引数:9.3万
J
Joshua Gorham
H 指数:40论文数:131被引数:1.1万
B
Barbara McDonough
H 指数:26论文数:70被引数:8,343
B
Bruce D. Gelb
H 指数:95论文数:497被引数:3.8万
S
Sarah U. Morton
H 指数:29论文数:217被引数:7,258
E
Elizabeth Goldmuntz
H 指数:68论文数:471被引数:1.7万
J
Jon A. L. Willcox
H 指数:13论文数:29被引数:898
W
Wendy K. Chung
H 指数:127论文数:1,272被引数:7.2万
M
Martina Brueckner
H 指数:44论文数:123被引数:1.0万