Aaron Chapla

ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 18

Top Venues

Endocrine

Clinical and translational science

The American Journal of dermatopathology

Indian journal of pediatrics

Joslin Diabetes Center

CHRISTIAN MEDICAL COLLEGE (PHD)

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

Affiliation History

Joslin Diabetes Center

United States

Research Fellow (ICMR-DHR IF) :: Section of Islet Cell and Regenerative Biology

CHRISTIAN MEDICAL COLLEGE Mar 16 2019

India

LECTURER GR I / ASSISTANT PROFESSOR :: ENDOCRINOLOGY

CHRISTIAN MEDICAL COLLEGE Mar 16 2016 - Mar 15 2019

India

LECTURER GR II / ASSISTANT PROFESSOR :: ENDOCRINOLOGY

CHRISTIAN MEDICAL COLLEGE

India

ASSOCIATE RESEARCH OFFICER :: ENDOCRINOLOGY

CHRISTIAN MEDICAL COLLEGE

India

ASSOCIATE RESEARCH OFFICER :: HAEMATOLOGY

Education History

CHRISTIAN MEDICAL COLLEGE

India

PHD :: ENDOCIRNOLOGY

CHRISTIAN MEDICAL COLLEGE

India

MSC :: BIOCHEMISTRY

Publications

Sumith K Mathew, Aaron Chapla, Padmanaban Venkatesan, Vishnu Eriyat, Blessed Winston Aruldhas, Ratna Prabha, Michael Noel Neely, Shoma V Rao, Subramani Kandasamy, Binu Susan Mathew
Genetic predisposition and high exposure to colistin in the early treatment period as independent risk factors for colistin-induced nephrotoxicity. Clinical and translational science 17 (3) (2024)
Lavanya Ravichandran, Shriti Paul, Rekha A, Asha Hs, Sarah Mathai, Anna Simon, Sumita Danda, Nihal Thomas, Aaron Chapla
High carrier frequency of CYP21A2 gene mutations in Southern India - underscoring the need for genetic testing in Congenital Adrenal Hyperplasia. Endocrine 85 (1) (2024)
Sumith K Mathew, Aaron Chapla, Padmanaban Venkatesan, Vishnu Eriyat, Blessed Winston Aruldhas, Ratna Prabha, Michael Noel Neely, Shoma V Rao, Subramani Kandasamy, Binu Susan Mathew
Genetic predisposition and high exposure to colistin in the early treatment period as independent risk factors for colistin-induced nephrotoxicity. Clinical and translational science 17 (3) (2024)
Adithya Christopher Godfred, Zachariah Thomas, Dincy Peter, Anjana Joseph, Lavanya Ravichandran, Anu Anna George, Susanne A Pulimood, Pranay Gaikwad, Ramesh Babu, Meera Thomas, Nihal Thomas, Aaron Chapla
A Novel Large Deletion in the EVER1 Gene in a Family With Epidermodysplasia Verruciformis From India. The American Journal of dermatopathology 46 (6) (2024)
Adithya Christopher Godfred, Zachariah Thomas, Dincy Peter, Anjana Joseph, Lavanya Ravichandran, Anu Anna George, Susanne A Pulimood, Pranay Gaikwad, Ramesh Babu, Meera Thomas, Nihal Thomas, Aaron Chapla
A Novel Large Deletion in the EVER1 Gene in a Family With Epidermodysplasia Verruciformis From India. The American Journal of dermatopathology (2024)
Lavanya Ravichandran, Shriti Paul, Rekha A, Asha Hs, Sarah Mathai, Anna Simon, Sumita Danda, Nihal Thomas, Aaron Chapla
High carrier frequency of CYP21A2 gene mutations in Southern India - underscoring the need for genetic testing in Congenital Adrenal Hyperplasia. Endocrine (2024)
Lavanya Ravichandran, Shriti Paul, Rekha A, Asha Hs, Sarah Mathai, Anna Simon, Sumita Danda, Nihal Thomas, Aaron Chapla
High carrier frequency of CYP21A2 gene mutations in Southern India - underscoring the need for genetic testing in Congenital Adrenal Hyperplasia. Endocrine 85 (1) (2024)
Ajoy Oommen John, Ashish Singh, Pratibha Yadav, Anjana Joel, Divya Bala Thumaty, K Fibi Ninan, Josh Thomas Georgy, Anish Jacob Cherian, Shawn Thomas, Anitha Thomas, Vinotha Thomas, Abraham Peedicayil, Deny Varghese, R Parthiban, Lavanya Ravichandran, Jabasteen Johnson, Nihal Thomas, Bijesh Yadav, Patricia S, B Selvamani, Deepak Abraham, M J Paul, Raju Titus Chacko, Aaron Chapla
The BRCA mutation spectrum among breast and ovarian cancers in India: highlighting the need to screen BRCA1 185delAG among South Indians. European journal of human genetics : EJHG (2024)
Lavanya Ravichandran, Shriti Paul, A Rekha, Deny Varghese, R Parthiban, H S Asha, Sarah Mathai, Anna Simon, Sumita Danda, Nihal Thomas, Aaron Chapla
Advocating Targeted Sequential Screening over Whole Exome Sequencing in 21-Hydroxylase Deficiency. Indian journal of pediatrics (2024)
Lavanya Ravichandran, Shriti Paul, Rekha A, Asha Hs, Sarah Mathai, Anna Simon, Sumita Danda, Nihal Thomas, Aaron Chapla
High carrier frequency of CYP21A2 gene mutations in Southern India - underscoring the need for genetic testing in Congenital Adrenal Hyperplasia. Endocrine 85 (1) (2024)
Sumith K Mathew, Aaron Chapla, Padmanaban Venkatesan, Vishnu Eriyat, Blessed Winston Aruldhas, Ratna Prabha, Michael Noel Neely, Shoma V Rao, Subramani Kandasamy, Binu Susan Mathew
Genetic predisposition and high exposure to colistin in the early treatment period as independent risk factors for colistin-induced nephrotoxicity. Clinical and translational science 17 (3) (2024)
Adithya Christopher Godfred, Zachariah Thomas, Dincy Peter, Anjana Joseph, Lavanya Ravichandran, Anu Anna George, Susanne A Pulimood, Pranay Gaikwad, Ramesh Babu, Meera Thomas, Nihal Thomas, Aaron Chapla
A Novel Large Deletion in the EVER1 Gene in a Family With Epidermodysplasia Verruciformis From India. The American Journal of dermatopathology 46 (6) (2024)
Rajan Palui, Lavanya Ravichandran, Sadish Kumar Kamalanathan, Aaron Chapla, Jaya Prakash Sahoo, Niya Narayanan, Dukhabandhu Naik, Nihal Thomas
Clinical, Hormonal, and Genetic Spectrum of 46 XY Disorders of Sexual Development (DSD) Patients. Indian journal of pediatrics (2024)
Aaron Chapla, Jabasteen Johnson, Sophy Korula, Nisha Mohan, Anish Ahmed, Deny Varghese, Parthiban Rangasamy, Lavanya Ravichandran, Felix Jebasingh, Krishna Kumar Agrawal, Noel Somasundaram, Asha Hesarghatta Shyamasunder, Sarah Mathai, Anna Simon, Sujeet Jha, Subhankar Chowdry, Radha Venkatesan, Palany Raghupathy, Nihal Thomas
WFS1 Gene-associated Diabetes Phenotypes and Identification of a Founder Mutation in Southern India. The Journal of clinical endocrinology and metabolism 107 (5) (2022)
Venkata Sandeep Nandipati, Aaron Chapla, Felix K Jebasingh, Arun Paul Charlu, Thilak Samuel Jepegnanam, Kripa Elizabeth Cherian, Thomas V Paul, Nihal Thomas
Cathepsin K Mutation-A Subtle Clinical Presentation. Journal of the Endocrine Society 6 (8) (2022)
Minu Jose Chiramel, Lydia Mathew, Rekha A, Aaron Chapla, Dharshini Sathishkumar, Thenmozhi Mani, Sumita Danda, Renu George
Genotype of autosomal recessive congenital ichthyosis from a tertiary care center in India. Pediatric dermatology 39 (3) (2022)
Eric Lontchi-Yimagou, Riddhi Dasgupta, Shajith Anoop, Sylvia Kehlenbrink, Sudha Koppaka, Akankasha Goyal, Padmanaban Venkatesan, Roshan Livingstone, Kenny Ye, Aaron Chapla, Michelle Carey, Arun Jose, Grace Rebekah, Anneka Wickramanayake, Mini Joseph, Priyanka Mathias, Anjali Manavalan, Mathews Edatharayil Kurian, Mercy Inbakumari, Flory Christina, Daniel Stein, Nihal Thomas, Meredith Hawkins
An Atypical Form of Diabetes Among Individuals With Low BMI. Diabetes care 45 (6) (2022)
Manickavasagam Senthilraja, Aaron Chapla, Felix K Jebasingh, Dukhabhandhu Naik, Thomas Vizhalil Paul, Nihal Thomas
Parallel Multi-Gene Panel Testing for Diagnosis of Idiopathic Hypogonadotropic Hypogonadism/Kallmann Syndrome. Case reports in genetics 2019 (2019)

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Publication Activity (10 Years)

Top Topics

Top Venues

Aaron Chapla