Manifestation of Hawkinsinuria in a patient compound heterozygous for Hawkinsinuria and Tyrosinemia III, Mol Genet Metab. 2007 Aug; 91 (4) : 379 - 83. Epub 2007 Jun 7.

Arthrogryposis- Bio Med., July 1999 issue.

Neonatal Hyper lysinemia A Cause of Severe Birth Asphyxia, Paper submitted in IAP Mumbai conference, Oct. 1999, Pg. FP 1 10.

Non immune Hydrops Foetails Bio Med., Dec. 1999, Pg. 128 132.

SIDS, A Composite of Doom Bio Med., Feb. 2000 issue Pg. 32 34.

Sudden Infant Death Syndrome Perinatology, 2000, Vol. 2 Number 4, Pg. 177 - 186.

Thyroid Function Tests in Sick Neonates Perinatology 2000, Vol. 2 Number 6, Pg. 265 274.

Inborn Errors of Metabolism in Critically ill Newborns Part 1 Perinatology 2001, Vol. 3, No.1: Pg. 13 24.

Inborn Errors of Metabolism in Critically ill Newborns Part II Perinatology 2001, Vol. 3 and No. 3: Pg. 113 121.

3 Hydroxy 3 Methylglutaric Aciduria (HMG Co A Lyase deficiency) Quarterly journal of Mumbai IAP Brach Impression Vol.1 Issue No. 2, July 2001; Page 16, 23.

Neonatal Metabolic and Genetic Disorders a book on Genetic and metabolic disorders for Pediatricians and Gynecologists; published in Jan. 2000.

Toxoplasmosis Perinatology Vol. 4 (2): 75 83.

Toxoplasmosis Perinatology Vol.4 (3): 134 147.

Newborn Screening in India Presented a research Paper at National Conference of ISPAT at Pune Jan. 2002.

Biotinidase deficiency screening in High risk newborn and pediatric population of India. Research paper accepted for presentation at International Conference of Newborn Screening was held at Italy from 25th June 29th June 2002.

Newborn Screening for Galactosemia. Thesis completed by M.Sc. Student under my supervision at our center.

Biochemical Parameters of Mental Retardation Use of Ammonia as a screening procedure. Thesis completed by M.Sc. (Research) Student of Bombay University under my supervision at our center.

V.L.C.A.D. deficiency A. B. Jalan and B. Awasthi, Perinatology, Vol. 6 (4), July Aug. 2004; 197 202.

Galactosemia, Journal of Genetics, Screening and Health, Vol1 No. 2 June 2006: 33-44.

Biotinidase Deficiency Urgent Need for Newborn Screening in India. Journal of Genetics, Screening and Health, Vol 1 No 3 Nov 2006.

Fructose 1,6 Diphosphatase Deficiency. Journal of Genetics, Screening and Health, Vol 2 No 2 Apr-May-June 2007.

Incidence of Preventable IEM in Indian Children with mental Retardation Journal of Genetics, Screening and Health, Vol 3 No 1 Jan-Feb-Mar 2008.

Outcome and Management of Citrullinemia in Indian Society Journal of Genetics,Screening and Health, Vol.3 No. 2 Oct-Dec 2008, 22 32.

Co-Author :-

1. Monique Van Scherpenzeel, Sharita Timal,Anil Jalanet al, Diagnostic serum glycosylation profile in
patients with intellectual disability as a result of MAN1B1 deficiency, doi:10.1093/brain/awu019 Brain 2014: 1-9 [Received September 10, 2013. Revised December 6, 2013. Accepted December 15, 2013].