Search

Author/Creator Anand, Anuranjan

1. A linkage and exome study implicates rare variants of KANK4 and CAP2 in bipolar disorder in a multiplex family. (21st August 2019)

Authors:
Anjanappa, Ram M.; Nayak, Sourav; Moily, Nagaraj S.; Manduva, Vallikiran; Nadella, Ravi K.; Viswanath, Biju; Reddy, Yemmiganur C. J.; Jain, Sanjeev; Anand, Anuranjan
Journal:
Bipolar disorders
Issue:
Volume 22:Number 1(2020)
Page Start:
70
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. Exome sequencing and functional analyses revealed CETN1 variants leads to impaired cell division and male fertility. Issue 4 (1st September 2022)

Authors:
Sudhakar, Digumarthi V S; Phanindranath, Regur; Jaishankar, Shveta; Ramani, Anand; Kalamkar, Kaustubh P; Kumar, Umesh; Pawar, Asmita D; Dada, Rima; Singh, Rajender; Gupta, Nalini J; Deenadayal, Mamata; Tolani, Aarti Deenadayal; Sharma, Yogendra; Anand, Anuranjan; Gopalakrishnan, Jay; Thangaraj, K...
Journal:
Human molecular genetics
Issue:
Volume 32:Issue 4(2023)
Page Start:
533
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. Functional Analysis of a Novel Connexin30 Mutation in a Large Family with Hearing Loss, Pesplanus, Ichthyosis, Cutaneous Nodules, and Keratoderma. (30th November 2015)

Authors:
Pandey, Nishtha; Xavier, Dennis F.; Chatterjee, Arunima; Mani, Ram‐Shankar; Hiremagalore, Ravi; Tharakan, Ajith; Rajashekhar, B.; Anand, Anuranjan
Journal:
Annals of human genetics
Issue:
Volume 80:Number 1(2016:Jan.)
Page Start:
11
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗