Roopa Kanakatti Shankar
Overview
Explore the profile of Roopa Kanakatti Shankar including associated specialties, affiliations and a list of published articles.
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34
Citations
290
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Recent Articles
1.
Shankar R, Quigley C, Isojima T, Mauras N, Chernausek S, Wasniewska M, et al.
Am J Med Genet C Semin Med Genet
. 2025 Feb;
:e32133.
PMID: 39950365
Short stature is a common presenting feature and an important concern for families of children with Turner syndrome. In this review, we summarize the data that shaped the updated international...
2.
Fezza J, Rau S, Clary L, Nimene Johnson O, Fimmel F, Barber J, et al.
Front Endocrinol (Lausanne)
. 2024 Dec;
15:1461103.
PMID: 39624818
Introduction: Turner syndrome (TS) is associated with significant neuropsychological challenges, and screening is recommended at key transition stages. Our goal was to describe the institutional experience of formal neuropsychological assessments...
3.
Shankar R, Gravholt C, Backeljauw P
Am J Med Genet C Semin Med Genet
. 2024 Nov;
:e32124.
PMID: 39610314
Turner syndrome was recognized nearly 90 years ago as a distinctive condition and the understanding of pathophysiology, and phenotype has incrementally and substantially changed along with the goals of treatment....
4.
Dowlut-McElroy T, Long J, Mayhew A, Lawson A, Fei Y, Smith A, et al.
J Pediatr Adolesc Gynecol
. 2024 Nov;
38(2):154-160.
PMID: 39577758
Study Objective: To evaluate the prevalence of germ cell tumors and the clinical monitoring practices for those who deferred prophylactic gonadectomy in a large North American cohort of individuals with...
5.
Galetaki D, Zhang A, Qi Y, Merchant N, Shankar R, Boucher K, et al.
Horm Res Paediatr
. 2024 Oct;
:1-7.
PMID: 39427650
Introduction: Vosoritide is a C-type natriuretic peptide (CNP) analog that binds its receptor on chondrocytes, promoting growth by inhibiting the ERK1/2-MAPK pathway. We previously reported the results of a phase...
6.
Klamut N, Bothwell S, Carl A, Bamba V, Law J, Brickman W, et al.
Am J Med Genet A
. 2024 Jul;
194(12):e63819.
PMID: 39016627
Turner syndrome (TS) is defined by partial or complete absence of a sex chromosome. Little is known about the phenotype of individuals with TS mosaic with trisomy X (45,X/47,XXX or...
7.
Patel T, Longendyke R, Shankar R, Merchant N
Endocrinol Diabetes Metab Case Rep
. 2024 Jun;
2024(2).
PMID: 38920131
Summary: Iodine nutrition is a growing issue within the USA due to newer trends of non-iodized salts. There are no recent reviews looking at the current state of iodine deficiency-induced...
8.
Dauber A, Zhang A, Shankar R, Boucher K, McCarthy T, Shafaei N, et al.
EClinicalMedicine
. 2024 May;
71:102591.
PMID: 38813446
Background: Hypochondroplasia is a rare autosomal dominant skeletal dysplasia due to activating variants in . It presents with disproportionate short stature with a wide range of clinical severity. There are...
9.
Gravholt C, Andersen N, Christin-Maitre S, Davis S, Duijnhouwer A, Gawlik A, et al.
Eur J Endocrinol
. 2024 May;
190(6):G53-G151.
PMID: 38748847
Turner syndrome (TS) affects 50 per 100 000 females. TS affects multiple organs through all stages of life, necessitating multidisciplinary care. This guideline extends previous ones and includes important new...
10.
Alkhatib E, Bartlett D, Shankar R, Regier D, Merchant N
Front Endocrinol (Lausanne)
. 2024 Jan;
14:1297335.
PMID: 38288475
Introduction: Type 1 pseudohypoaldosteronism (PHA) consists of resistance to aldosterone. Neonatal presentation is characterized by salt wasting, hyperkalemia, and metabolic acidosis with high risk of mortality. Type 1 PHA can...