Inusha Panigrahi

Scopus Author ID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 29

Top Venues

American journal of medical genetics. Part A

Journal of pediatric genetics

Case reports in genetics

BMJ case reports

Post Graduate Institute of Medical Education and Research

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Post Graduate Institute of Medical Education and Research Jul 01 2016

India

Professor :: Pediatrics

All India Institute of Medical Sciences Jan 01 2003 - Dec 31 2005

India

Pool Officer-SRA :: Hematology

Sanjay Gandhi Post Graduate Institute of Medical Sciences Jan 01 1999 - Dec 31 2001

India

DM_SR :: Genetics

Publications

Anil Kumar Bhalla, Harvinder Kaur, Rupinder Kaur, Inusha Panigrahi
Growth charts for weight and height of Indian children with Down syndrome. American journal of medical genetics. Part A (2024)
Naseebullah Kakar, Fazal Ur Rehman, Ramandeep Kaur, Gandham SriLakshmi Bhavani, Manisha Goyal, Hitesh Shah, Karandeep Kaur, Kushaljit Singh Sodhi, Christian Kubisch, Guntram Borck, Inusha Panigrahi, Katta Mohan Girisha, Uwe Kornak, Malte Spielmann
Multi-gene panel sequencing in highly consanguineous families and patients with congenital forms of skeletal dysplasias. Clinical genetics 106 (1) (2024)
Anil Kumar Bhalla, Harvinder Kaur, Rupinder Kaur, Inusha Panigrahi
Growth charts for weight and height of Indian children with Down syndrome. American journal of medical genetics. Part A 194 (7) (2024)
Amit Singh, Sabyasachi Senapati, Inusha Panigrahi, Preeti Khetarpal
Novel Compound Heterozygous Mutations of LIG4 Gene in an Indian LIG4 Syndrome Patient with Severe Microcephaly: Case Report, In-silico Analysis and Systematic Review. Current pediatric reviews (2024)
Inusha Panigrahi, Sudha Rao, Shalu Verma Kumar, Divya Kumari, Parminder Kaur
Intellectual Disability and Blended Phenotypes: Insights from a Centre in North India. Case reports in genetics 2024 (2024)
Anil Kumar Bhalla, Harvinder Kaur, Rupinder Kaur, Inusha Panigrahi
Growth charts for weight and height of Indian children with Down syndrome. American journal of medical genetics. Part A 194 (7) (2024)
Naseebullah Kakar, Fazal Ur Rehman, Ramandeep Kaur, Gandham SriLakshmi Bhavani, Manisha Goyal, Hitesh Shah, Karandeep Kaur, Kushaljit Singh Sodhi, Christian Kubisch, Guntram Borck, Inusha Panigrahi, Katta Mohan Girisha, Uwe Kornak, Malte Spielmann
Multi-gene panel sequencing in highly consanguineous families and patients with congenital forms of skeletal dysplasias. Clinical genetics (2024)
Amit Singh, Ketan Pajni, Inusha Panigrahi, Navdeep Dhoat, Sabyasachi Senapati, Preeti Khetarpal
Components of IGF-axis in growth disorders: a systematic review and patent landscape report. Endocrine 76 (3) (2022)
Nandita Sharma, Divya Kumari, Inusha Panigrahi, Preeti Khetarpal
A systematic review of the monogenic causes of Non-Syndromic Hearing Loss (NSHL) and discussion of Current Diagnosis and Treatment options. Clinical genetics (2022)
Inusha Panigrahi, Yogita Bhatt, Shivani Malik, Parminder Kaur, Anupriya Kaur
Clinical Profile of Indian Children with Down Syndrome. Journal of pediatric genetics 12 (1) (2021)
Parminder Kaur, Inusha Panigrahi, Harleen Kaur, Thakurvir Singh, Chakshu Chaudhry
Overlapping Phenotypes in Osteopetrosis and Pycnodysostosis in Asian-Indians. Case reports in genetics 2021 (2021)
Parminder Kaur, Chakshu Chaudhry, Harsha Neelam, Inusha Panigrahi
Bardet-Biedl syndrome presenting with laryngeal web and bifid epiglottis. BMJ case reports 14 (1) (2021)
Prabakaran Gangadaran, Chakshu Chaudhry, Inusha Panigrahi, Anu Kumari, Anupriya Kaur
X-linked frontometaphyseal dysplasia with severe scoliosis and spinal cord compromise in an Indian boy. American journal of medical genetics. Part A 185 (5) (2021)
Chakshu Chaudhry, Divya Kumari, Inusha Panigrahi, Parminder Kaur
Chromosome 1p36 Deletion Syndrome: Four Patients with Variable Presentations. Journal of pediatric genetics 12 (4) (2021)
Chakshu Chaudhry, Divya Kumari, Inusha Panigrahi, Parminder Kaur
Chromosome 1p36 Deletion Syndrome: Four Patients with Variable Presentations. Journal of pediatric genetics 12 (4) (2021)
Inusha Panigrahi, Yogita Bhatt, Shivani Malik, Parminder Kaur, Anupriya Kaur
Clinical Profile of Indian Children with Down Syndrome. Journal of pediatric genetics 12 (1) (2021)
Inusha Panigrahi, Parminder Kaur, Chakshu Chaudhry, Mohd Shariq, Devika D Naorem, B C Gowtham, Anupriya Kaur, Devi Dayal
Short Stature Syndromes: Case Series from India. Journal of pediatric genetics 11 (4) (2021)
Chakshu Chaudhry, Parminder Kaur, Priyanka Srivastava, Inusha Panigrahi, Anupriya Kaur
Novel variation in ANTXR2 gene causing hyaline fibromatosis syndrome: A report from India. Congenital anomalies 61 (4) (2021)
Deepanjan Bhattacharya, Inusha Panigrahi, Chakshu Chaudhry
Clinical profile of symptomatic congenital cytomegalovirus infection: cases from a tertiary hospital in north India. Tropical doctor 50 (3) (2020)
Inusha Panigrahi, Yousaf Qureshi, Uwe Kornak
Over-Representation of Recessive Osteogenesis Imperfecta in Asian Indian Children. Journal of pediatric genetics 11 (1) (2020)
Inusha Panigrahi, Chakshu Chaudhry
Sotos syndrome in two children from India. American journal of medical genetics. Part A 182 (9) (2020)
Inusha Panigrahi, Bangalore Anantharamu Shankar Prasad, Harleen Kaur, Jasvinder Kalra
COFS type 3 in an Indian family with antenatally detected arthrogryposis. American journal of medical genetics. Part A 185 (2) (2020)
Chakshu Chaudhry, Anit Kaur, Inusha Panigrahi, Anupriya Kaur
Wolf-Hirschhorn syndrome: A case series from India. American journal of medical genetics. Part A 182 (12) (2020)
Inusha Panigrahi, Chirag Ahuja, Chakshu Chaudhry
Indian child with novel variant in OFD1 gene. American journal of medical genetics. Part A 182 (10) (2020)
Inusha Panigrahi, Manoj Dhanorkar, Renu Suthar, Chanchal Kumar, Mullai Baalaaji, Babu Ram Thapa, Jasvinder Kalra
Niemann-Pick Disease: An Underdiagnosed Lysosomal Storage Disorder. Case reports in genetics 2019 (2019)
Deepanjan Bhattacharya, Anil Kumar Bn, Inusha Panigrahi, Anupriya Kaur
Hepatomegaly with neutropenia: a girl with glycogen storage disease Ib. BMJ case reports 12 (7) (2019)
Inusha Panigrahi, Manoj Dhanorkar, Siyaram Didel, Raja Ashok Koganti
Hunter syndrome with persistent thrombocytopenia. BMJ case reports 12 (4) (2019)
Sapna Sandal, Anupriya Kaur, Inusha Panigrahi
Novel mutation in the CHST14 gene causing musculocontractural type of Ehlers-Danlos syndrome. BMJ case reports 2018 (2018)
Inusha Panigrahi, Savita Bhunwal, Harish Varma, Simranjeet Singh
Methylmalonic Acidemia with Novel MUT Gene Mutations. Case reports in genetics 2017 (2017)

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Publication Activity (10 Years)

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Inusha Panigrahi