Seema Mital

Also affiliated with Hospital for Sick Children, Ted Rogers Centre for Heart Research

MedicineBiochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 11 papers. Top paper: “Intrinsic Endocardial Defects Contribute to Hypoplastic Left Heart Syndrome”.

Intrinsic Endocardial Defects Contribute to Hypoplastic Left Heart Syndrome

Cell stem cell(2020)10.1016/j.stem.2020.07.015

N/A

0DataRank · unranked

172 citations

Lei Tian, Marcy Martin, Sharon L. Paige, Francisco X. Galdos, Jibiao Li +18 more

Variants in ADRB1 and CYP2C9: Association with Response to Atenolol and Losartan in Marfan Syndrome

The Journal of Pediatrics(2020)10.1016/j.jpeds.2020.03.064

N/A

0DataRank · unranked

17 citations

Lynn A. Sleeper, Bruce D. Gelb, Shaine A. Morris, Harry C. Dietz, Geoffrey A. Forbus +19 more

Lifespan Perspective on Congenital Heart Disease Research

Journal of the American College of Cardiology(2021)10.1016/j.jacc.2021.03.012

N/A

0DataRank · unranked

106 citations

Alexandra Arvanitaki, Alexander R. Opotowsky, Kathy J. Jenkins, Philip Moons, Alexander Kempny +8 more

Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot

Genetics in Medicine(2021)10.1038/s41436-021-01212-y

N/A

0DataRank · unranked

17 citations

Najim Lahrouchi, Fernanda M. Bosada, Gregor Dombrowsky, Simon G. Williams, Robert Lesurf +49 more

Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease

Human Genetics and Genomics Advances(2021)10.1016/j.xhgg.2021.100037

N/A

0DataRank · unranked

15 citations

Wenjuan Zhu, George C. Gabriel, Cullen B. Young, Kylia Williams, Lisa J. Martin +36 more

An Integrated Clinical and Genetic Prediction Model for Tacrolimus Levels in Pediatric Solid Organ Transplant Recipients

Transplantation(2021)10.1097/tp.0000000000003700

N/A

0DataRank · unranked

14 citations

Tanya Papaz, A. Nicole Lambert, Upton Allen, Patricia Birk, Tom Blydt-Hansen +15 more

KMT2D-NOTCH Mediates Coronary Abnormalities in Hypoplastic Left Heart Syndrome

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.08.30.457716

N/A

0DataRank · unranked

0 citations

Xin Zhou, Ziyi Liu, Victor Pastrana-Gomez, Yu Liu, Minzhe Guo +12 more

JAGGED1/NOTCH3 activation promotes aortic hypermuscularization and stenosis in elastin deficiency

Journal of Clinical Investigation(2022)10.1172/jci142338

N/A

0DataRank · unranked

37 citations

Raja Chakraborty, Aglaia Ntokou, Junichi Saito, Fatima Z. Saddouk, Zhonghui Feng +11 more

Rare variants in CAPN2 increase risk for isolated hypoplastic left heart syndrome

Human Genetics and Genomics Advances(2023)10.1016/j.xhgg.2023.100232

N/A

0DataRank · unranked

2 citations

Janson J. White, Michael Dush, William W. Gordon, Brent Wyatt, Peter White +22 more

Myosin inhibitor reverses hypertrophic cardiomyopathy in pediatric iPSC-cardiomyocytes to mirror variant correction

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.04.14.536782

N/A

0DataRank · unranked

0 citations

Abdelrahman Said, Guoliang Meng, Yimu Zhao, Erika Y Wang, Neha Parmar +7 more

Myosin inhibitor reverses hypertrophic cardiomyopathy in genotypically diverse pediatric iPSC-cardiomyocytes to mirror variant correction

Cell Reports Medicine(2024)10.1016/j.xcrm.2024.101520

N/A

0DataRank · unranked

19 citations

Abdelrahman Said, Guoliang Meng, Yimu Zhao, Erika Y. Wang, Naimeh Rafatian +8 more