User profiles for S. LALANI

Sarfaraz Lalani

- Verified email at csmc.edu - Cited by 992

Salima Lalani

- Verified email at amc.edu - Cited by 885

Endometriosis and adverse maternal, fetal and neonatal outcomes, a systematic review and meta-analysis

S Lalani, AJ Choudhry, B Firth, V Bacal… - Human …, 2018 - academic.oup.com
STUDY QUESTION How is endometriosis associated with adverse maternal, fetal and
neonatal outcomes of pregnancy? SUMMARY ANSWER Women with endometriosis are at …

[HTML][HTML] Flavonoids as Antiviral Agents for Enterovirus A71 (EV-A71)

S Lalani, CL Poh - Viruses, 2020 - mdpi.com
… The IC 50 was found to be 0.63 µM in 293 S cells and 66.67% newborn BALB/c mice survived
the lethal challenge with EV-A71 when mice were treated with 5 mg/Kg dose of penduletin …

[HTML][HTML] Centers for Mendelian Genomics: A decade of facilitating gene discovery

…, M Khayat, J Knight, JT Kolar, S Kumar, S Lalani… - Genetics in …, 2022 - Elsevier
Purpose Mendelian disease genomic research has undergone a massive transformation
over the past decade. With increasing availability of exome and genome sequencing, the role …

Recurrent reciprocal 1q21. 1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities

…, F Scaglia, J Belmont, CA Bacino, T Sahoo, SR Lalani… - Nature …, 2008 - nature.com
Chromosome region 1q21.1 contains extensive and complex low-copy repeats, and copy
number variants (CNVs) in this region have recently been reported in association with …

Discovery of a periosteal stem cell mediating intramembranous bone formation

S Debnath, AR Yallowitz, J McCormick, S Lalani… - Nature, 2018 - nature.com
… For comparisons of three or more groups, one-way ANOVA was used if normality tests passed,
followed by Tukey’s multiple comparison test for all pairs of groups. If normality tests failed…

[HTML][HTML] Chromosome catastrophes involve replication mechanisms generating complex genomic rearrangements

…, D Hernández-Almaguer, LD Immken, SR Lalani… - Cell, 2011 - cell.com
Complex genomic rearrangements (CGRs) consisting of two or more breakpoint junctions
have been observed in genomic disorders. Recently, a chromosome catastrophe …

[PDF][PDF] Spectrum of CHD7 mutations in 110 individuals with CHARGE syndrome and genotype-phenotype correlation

SR Lalani, AM Safiullah, SD Fernbach… - The American Journal of …, 2006 - cell.com
… at 94C for 30 s and annealing at 60C for 90 s, and a final extension at 72C for 60 s. An
annealing … Biosystems) by use of the manufacturer’s standard protocol and reagents. Sequence …

Functional impairment in COPD patients: the impact of anxiety and depression

HFS Kim, ME Kunik, VA Molinari, SL Hillman, S Lalani… - Psychosomatics, 2000 - Elsevier
The authors examined the relationship between functional status and comorbid anxiety and
depression and the relationship between utilization of health care resources and …

Use of exome sequencing for infants in intensive care units: ascertainment of severe single-gene disorders and effect on medical management

…, W Bi, F Xia, B Lee, CM Eng, Y Yang, SR Lalani - JAMA …, 2017 - jamanetwork.com
Importance While congenital malformations and genetic diseases are a leading cause of
early infant death, to our knowledge, the contribution of single-gene disorders in this group is …

[PDF][PDF] High rate of recurrent de novo mutations in developmental and epileptic encephalopathies

…, SR Lalani, RE Frye, IT Jarjour, S Jacques… - The American Journal of …, 2017 - cell.com
Developmental and epileptic encephalopathy (DEE) is a group of conditions characterized
by the co-occurrence of epilepsy and intellectual disability (ID), typically with developmental …