1. A Child Presenting with Recurrent Corneal Ulcers: Hereditary Sensory and Autonomic Neuropathy IV (HSAN IV). (3rd September 2019) Authors: Suresh, Beena; Reddy, Vaishnavi; Kurth, Ingo; Jagadeesh, Sujatha Journal: Neuro-ophthalmology Issue: Volume 43:Number 5(2019) Page Start: 310 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Bain type of X‐linked syndromic mental retardation in a male with a pathogenic variant in HNRNPH2. Issue 1 (31st October 2019) Authors: Somashekar, Puneeth H.; Narayanan, Dhanya L.; Jagadeesh, Sujatha; Suresh, Beena; Vaishnavi, Reddy D.; Bielas, Stephanie; Girisha, Katta M.; Shukla, Anju Journal: American journal of medical genetics Issue: Volume 182:Issue 1(2020) Page Start: 183 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Featured Cover. Issue 6 (2nd May 2021) Authors: Rezaei, Maryam; Suresh, Beena; Bereke, Eric; Hadipour, Zahra; Aguinaga, Monic; Qian, Jianhua; Bagga, Rashmi; Fardaei, Majid; Hemida, Reda; Jagadeesh, Sujatha; Majewski, Jacek; Slim, Rima Journal: Clinical genetics Issue: Volume 99:Issue 6(2021) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Novel pathogenic variants in NLRP7, NLRP5, and PADI6 in patients with recurrent hydatidiform moles and reproductive failure. Issue 6 (23rd February 2021) Authors: Rezaei, Maryam; Suresh, Beena; Bereke, Eric; Hadipour, Zahra; Aguinaga, Monica; Qian, Jianhua; Bagga, Rashmi; Fardaei, Majid; Hemida, Reda; Jagadeesh, Sujatha; Majewski, Jacek; Slim, Rima Journal: Clinical genetics Issue: Volume 99:Issue 6(2021) Page Start: 823 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Ptosis as a unique hallmark for autosomal recessive WNT1‐associated osteogenesis imperfecta. Issue 6 (21st March 2019) Authors: Nampoothiri, Sheela; Guillemyn, Brecht; Elcioglu, Nursel; Jagadeesh, Sujatha; Yesodharan, Dhanya; Suresh, Beena; Turan, Serap; Symoens, Sofie; Malfait, Fransiska Journal: American journal of medical genetics Issue: Volume 179:Issue 6(2019) Page Start: 908 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Pyridoxine-dependent epilepsy owing to antiquitin deficiency — mutation in the ALDH7A1 gene. (1st May 2013) Authors: Jagadeesh, Sujatha; Suresh, Beena; Murugan, V; Suresh, S; Salomans, G S; Struys, E A; Jacobs, C Journal: Paediatrics and international child health Issue: Volume 33:Number 2(2013:May) Page Start: 113 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Pyridoxine-dependent epilepsy owing to antiquitin deficiency — mutation in the ALDH7A1 gene. (1st May 2013) Authors: Jagadeesh, Sujatha; Suresh, Beena; Murugan, V; Suresh, S; Salomans, G S; Struys, E A; Jacobs, C Journal: Paediatrics and international child health Issue: Volume 33:Number 2(2013:May) Page Start: 113 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Pyridoxine-dependent epilepsy owing to antiquitin deficiency — mutation in the ALDH7A1 gene. (May 2013) Authors: Jagadeesh, Sujatha; Suresh, Beena; Murugan, V; Suresh, S; Salomans, G S; Struys, E A; Jacobs, C Journal: Paediatrics and international child health Issue: Volume 33:Number 2(2013:May) Page Start: 113 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗