Seema R. Lalani

ScholarGPS® ID: 93270885422825

Affiliation

Baylor College of Medicine, Houston, United States

Affiliation History

Field

Life Sciences

Discipline

Genetics

Top Specialties

Metrics Summary

Publication Count

127

Predicted Citations

5,733

Predicted h-index

Ranking

Publications and Citation History

Publications based on Top Specialties

Types of Publication

Publications
Books
Patents
NIH/NSF

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Clinical exome sequencing uncovers genetic disorders in neonates with suspected hypoxic–ischemic encephalopathy: A retrospective analysis (journal article) Parobek, Christian M. \| Zemet, Roni \| Shanahan, Matthew A. \| Burnett, Brian A. \| Mizerik, Elizabeth \| Rosenfeld, Jill A. \| Vossaert, Liesbeth \| Clark, Steven L. \| Hunter, Jill V. \| Lalani, Seema R. Clinical Genetics, volume 106, issue 1, pages 95-101 (2024). 10.1111/cge.14522 Cite \| Source
Intracranial calcifications simulating Aicardi‐Goutières syndrome in PARS2 ‐related mitochondrial disease (journal article) Gerard, Amanda \| Mizerik, Elizabeth \| Mohila, Carrie A. \| AlAwami, Sarah \| Hunter, Jill V. \| Kearney, Debra L. \| Lalani, Seema R. \| Scaglia, Fernando American Journal of Medical Genetics Part A, volume 194, issue 7 (2024). 10.1002/ajmg.a.63589 Cite \| Source
Folate as a potential treatment for lethal ventricular arrhythmias in TANGO2-deficiency disorder (journal article) Xu, Weiyi \| Cao, Yingqiong \| Stephens, Sara B. \| Arredondo, Maria Jose \| Chen, Yifan \| Perez, William \| Sun, Liang \| Yu, Andy C. \| Kim, Jean J. \| Lalani, Seema R. \| ... \| Zhang, Lilei JCI Insight, volume 9, issue 11 (2024). 10.1172/jci.insight.171005 Cite \| Source
P871: Genetic insight, social impact: Transforming care through Sotos syndrome diagnosis (journal article) Brooks, Dan \| Mizerik, Elizabeth \| Vossaert, Liesbeth \| Lalani, Seema \| Weisz-Hubshman, Monika \| Potocki, Lorraine \| Robak, Laurie Genetics in Medicine Open, volume 2 (2024). 10.1016/j.gimo.2024.101785 Cite \| Source
P701: Novel presentation of dextrocardia in TGIF1-related holoprosencephaly (journal article) Thornton, Casey \| Owen, Nichole \| Mizerik, Elizabeth \| Rose, Chelsi \| Lalani, Seema \| Waskow, Emily \| Machol, Keren Genetics in Medicine Open, volume 2 (2024). 10.1016/j.gimo.2024.101605 Cite \| Source
P297: More than an extra chromosome: Unexpected multiple diagnoses in individuals with Down syndrome (journal article) Vossaert, Liesbeth \| Owen, Nichole \| Dai, Hongzheng \| Kao, Eric \| Zhao, Xiaonan \| Lalani, Seema \| Weisz-Hubshman, Monika \| Potocki, Lorraine \| Mizerik, Elizabeth Genetics in Medicine Open, volume 2 (2024). 10.1016/j.gimo.2024.101193 Cite \| Source
P050: Biallelic variants in POLG2 provides a rare molecular diagnosis in a patient with epilepsy and liver failure (journal article) Rossi, Vittoria \| Brooks, Dan \| Dai, Hongzheng \| Mizerik, Elizabeth \| Ben-Moshe, Yishay \| Lalani, Seema \| Scott, Daryl \| Scaglia, Fernando \| Machol, Keren \| Bekheirnia, Mir Reza Genetics in Medicine Open, volume 2 (2024). 10.1016/j.gimo.2024.100927 Cite \| Source
692 Genetic findings among neonates with perinatal hypoxic-ischemic encephalopathy (journal article) Parobek, Christian M. \| Shanahan, Matthew A. \| Lazar, Roni Zemet \| Burnett, Brian \| Mizerik, Elizabeth \| Rosenfeld, Jill \| Vossaert, Liesbeth \| Clark, Steven \| Hunter, Jill \| Lalani, Seema American Journal of Obstetrics and Gynecology, volume 230, issue 1, pages S371- (2024). 10.1016/j.ajog.2023.11.718 Cite \| Source
Lack of Methylation Changes in GJB2 and RB1 Non-coding Regions of Cochlear Implant Patients with Sensorineural Hearing Loss (journal article) Sumalde, Angelo Augusto \| Yang, Ivana \| Yarza, Talitha Karisse \| Tobias-Grasso, Celina Ann \| Tantoco, Ma. Leah \| Davidson, Elizabeth \| Chan, Abner \| Azamian, Mahshid \| Cruz, Teresa Luisa \| Lalani, Seema \| ... \| Chiong, Charlotte Acta Medica Philippina, volume 57, issue 9 (2023). 10.47895/amp.v57i9.5200 Cited by (1) \| Cite \| Source
A Multicenter Analysis of Abnormal Chromosomal Microarray Findings in Congenital Heart Disease (journal article) Landis, Benjamin J. \| Helvaty, Lindsey R. \| Geddes, Gabrielle C. \| Lin, Jiuann‐Huey Ivy \| Yatsenko, Svetlana A. \| Lo, Cecilia W. \| Border, William L. \| Wechsler, Stephanie Burns \| Murali, Chaya N. \| Azamian, Mahshid S. \| ... \| Ware, Stephanie M. Journal of the American Heart Association, volume 12, issue 18 (2023). 10.1161/JAHA.123.029340 Cited by (3) \| Cite \| Source
Early initiation of B ‐vitamin supplementation may reduce symptoms and explain intrafamilial variability: Insights from two sibling pairs from the TANGO2 natural history study (journal article) Miyake, Christina Y. \| Ehsan, Saad A. \| Zhang, Lilei \| Mackenzie, Samuel J. \| Azamian, Mahshid S. \| Scott, Daryl A. \| Hernandez‐Garcia, Andres \| Lalani, Seema R. American Journal of Medical Genetics Part A, volume 191, issue 9, pages 2433-2439 (2023). 10.1002/ajmg.a.63331 Cited by (4) \| Cite \| Source
Dominant Negative Variants in IKZF2 Cause ICHAD Syndrome, a New Disorder Characterized by Immunodysregulation, Craniofacial Anomalies, Hearing Impairment, Athelia, and Developmental Delay (journal article) Vaseghi-Shanjani, Maryam \| Mohajeri, Arezoo \| Rosenfeld, Jill A. \| Lu, Henry \| Sharma, Mehul \| Lalani, Seema \| Nicholas, Sarah \| Scott, Daryl A. \| Turvey, Stuart \| Lehman, Anna Clinical Immunology, volume 250 (2023). 10.1016/j.clim.2023.109546 Cited by (1) \| Cite \| Source
Response to Tofacitinib in an Infant with Aicardi-Goutières Syndrome due to Biallelic Variants in RNU7–1 (journal article) Nimri, Jena \| Nguyen, Jessica \| Lalani, Seema \| Patel, Kalyani \| Mysore, Krupa \| O’Garro, Ginelle \| Emrick, Lisa \| Tunuguntla, Hari \| Burrage, Lindsay \| Vogel, Tiphanie Clinical Immunology, volume 250 (2023). 10.1016/j.clim.2023.109539 Cite \| Source
Assigning pathogenicity for TAB2 variants using a novel scalable functional assay and expanding TAB2 disease spectrum (journal article) Xu, Weiyi \| Graves, Andrea \| Weisz-Hubshman, Monika \| Hegazy, Lamees \| Magyar, Christina \| Liu, Zian \| Nasiotis, Eleni \| Samee, Md Abul Hassan \| Burris, Thomas \| Lalani, Seema \| Zhang, Lilei Human Molecular Genetics, volume 32, issue 6, pages 959-970 (2023). 10.1093/hmg/ddac252 Cite \| Source
B‐complex vitamins for patients with TANGO2 ‐deficiency disorder (journal article) Sandkuhler, Sarah E. \| Zhang, Lilei \| Meisner, Joshua K. \| Ghaloul‐Gonzalez, Lina \| Beach, Cheyenne M. \| Harris, David \| de Lonlay, Pascale \| Lalani, Seema R. \| Miyake, Christina Y. \| Mackenzie, Samuel J. Journal of Inherited Metabolic Disease, volume 46, issue 2, pages 161-162 (2023). 10.1002/jimd.12585 Cited by (10) \| Cite \| Source
A multicenter cross-sectional study in infants with congenital heart defects demonstrates high diagnostic yield of genetic testing but variable evaluation practices (journal article) Durbin, Matthew D. \| Helvaty, Lindsey R. \| Li, Ming \| Border, William \| Fitzgerald-Butt, Sara \| Garg, Vidu \| Geddes, Gabrielle C. \| Helm, Benjamin M. \| Lalani, Seema R. \| McBride, Kim L. \| ... \| Ware, Stephanie M. Genetics in Medicine Open, volume 1, issue 1, pages 100814- (2023). 10.1016/j.gimo.2023.100814 Cited by (4) \| Cite \| Source
P374: Project GIVE: Expanding genetic testing to underserved areas in the Rio Grande Valley using a telehealth platform (journal article) Brooks, Dan \| Vuocolo, Blake \| Sierra, Roberta \| Holder, Christopher \| Urbanski, Lauren \| Berry, Lori \| Lizardo-Guzman, Segundo \| Hernandez, Ana \| Godoy, Jose Gamez \| Mulukutla, Surya \| ... \| Lalani, Seema Genetics in Medicine Open, volume 1, issue 1, pages 100410- (2023). 10.1016/j.gimo.2023.100410 Cite \| Source
P284: Compound heterozygosity for loss-of-function variants in GDF1 provides a molecular diagnosis in a patient with heterotaxy syndrome (journal article) Rossi, Vittoria \| Luo, Xi \| Nunez, Kristin Cardiel \| Yi, Ruiyang \| Mizerik, Elizabeth \| Westerfield, Lauren \| Lalani, Seema \| Bekheirnia, Mir Reza Genetics in Medicine Open, volume 1, issue 1, pages 100312- (2023). 10.1016/j.gimo.2023.100312 Cite \| Source
Clinical exome sequencing uncovers a high frequency of Mendelian disorders in infants with stroke: A retrospective analysis (journal article) Kumar, Runjun D. \| Meng, Linyan \| Liu, Pengfei \| Miyake, Christina Y. \| Worley, Kim C. \| Bi, Weimin \| Lalani, Seema R. American Journal of Medical Genetics Part A, volume 188, issue 11, pages 3184-3190 (2022). 10.1002/ajmg.a.62967 Cited by (3) \| Cite \| Source
Quality of life, illness perceptions, and parental lived experiences in TANGO2-related metabolic encephalopathy and arrhythmias (journal article) Murali, Chaya N. \| Lalani, Seema R. \| Azamian, Mahshid S. \| Miyake, Christina Y. \| Smith, Hadley Stevens European Journal of Human Genetics, volume 30, issue 9, pages 1044-1050 (2022). 10.1038/s41431-022-01127-5 Cited by (2) \| Cite \| Source