PubMed indexed journals
As First/Corresponding Author*

• Haldar A, Sharma AK, Phadke SR, Jain A, Agarwal SS. OEIS Complex with Cranio-Facial anomalies: Defect of Blastogenesis? Am J Med Genetics. 1994; 53: 21-23. (IF 2.578; Cited by 39) PMID: 7802030.
• Halder A*, Tutschek B. Analysis of meiotic segregation in human nondecondensed interphase spermatozoa by multicolor rapid direct FISH. Ind J Med Res. 1998; 107: 94-97. (IF 5.274; Cited by 11) PMID: 9540284.
• Halder A*, Pahi J, Pradhan M, Pandey A, Gujral R, Agarwal SS. Iniencephaly: a report of 19 cases. Ind Pediatrics. 1998; 35: 891 - 896. (IF 3.839; Cited by 15) PMID: 10216599.
• Halder A*, Pahi J, Sharma AK, Bhatia VL, Phadke RV, Gujral R & Agarwal SS. Osteodysplastic Primordial Dwarfism Type II with normal Mentation and delayed CNS Myelination. Am. J. Med. Genet. 1998; 80: 12-15. (IF 2.578; Cited by 12) PMID: 9800906.
• Halder A*, Park YK. Identification of the appropriate tissue from formalin fixed perinatal autopsy material for chromosomal ploidy detection by interphase FISH. Ind J Med Res. 1999; 110: 102-106. (IF 5.274; Cited by 09) PMID: 10612912.
• Halder A*, Pahi J, Chadda V and Agarwal SS. Sirenomelia Sequence associated with craniorachischisis totalis, limb reduction and primitive heart: a case report. Indian Pediatr. 2001; 38 (9): 1041-5. (IF 3.839; Cited by 19) PMID: 11568383.
• Chaddha V, Agarwal S, Phadke SR, Halder A*. Low Level of Mosaicism in Atypical Prader Willi Syndrome: Detection using Fluorescent In Situ Hybridization. Indian Pediatrics 2003; 40: 166-168. (IF 3.839; Cited by 10) PMID: 12626835.
• Halder A*, Panigrahi I & Pal L. Fowler like syndrome with extreme oligohydramnios & growth restriction and without muscle hypoplasia: first case from Indian subcontinent. Ind Pediat 2003; 40: 418-423. (IF 3.839; Cited by 11) PMID: 12768045.
• Halder A*, Chaddha V, Agarwal S, Fauzdar A. Absence of sperm meiotic segregation error of chromosomes 1, 9, 12, 13, 16, 18, 21, X and Y in a case of 100 % necrozoospermia. Asian J Androl. 2003 Jun; 5(2): 163-166. (IF 3.05; Cited by 09) PMID: 12778330.
• Halder A*, Agarwal S, Pandey A. Iniencephaly and Chromosome Mosaicism: A Report of Two Cases. Congenital Anomalies 2005; 45: 102-105. (IF 1.3; Cited by 13) PMID: 16131369.
• Halder A*, Fauzdar A, Kumar A. Serum Inhibin B and Follicle Stimulating Hormone Levels as Markers in the Evaluation of Azoospermic Men: A Comparison. Andrologia 2005; 37: 173-179. (IF 2.53; Cited by 50) PMID: 16266395.
• Halder A*, Fauzdar A, Kabra M and Saxena A. Detection of 22q11.2 hemizygous deletion by interphase FISH in a patient with features of CATCH22 Syndrome. Ind Pediatr. 2005; 42: 1236-1239. (IF 3.839; Cited by 05) PMID: 16424562.
• Halder A*, Halder S, Fauzdar A. A Preliminary Investigation on Molecular Basis for Clinical Aggressiveness in Cervical Carcinoma by Comparative Genomic Hybridization and Conventional Fluorescent In-situ Hybridization. Ind J of Med Res. 2005; 122: 434-446. (IF 5.274; Cited by 06) PMID: 16456259.
• Halder A*, Fauzdar A. Extreme Skewing of Sex Ratio and Low Aneuploidy in Recurrent Early Missed Abortion. Ind J Med Res 2006; 124: 41-50. (IF 5.274; Cited by 37) PMID: 16926455.
• Halder A*. Skewed Sex Ratio in India. Ind J Med Res 2006; 124: 583-584. (IF 5.274; Cited by 10) PMID: 17213528.
• Halder A*, Jain M, Kabra M, Gupta N. Mosaic 22q11.2 microdeletion syndrome: diagnosis and clinical manifestations of two cases. Molecular Cytogenetics 2008; 1: 18. (IF 1.9; Cited by 38) PMID: 18691436.
• Fauzdar A, Sharma RK, Kumar A, Halder A*. A Preliminary Study on Chromosome Aneuploidy and Mosaicism in Early Preimplantation Human Embryo by Fluorescence In Situ Hybridization. Ind J Med Res 2008; 128 (3): 287-293. (IF 5.274; Cited by 04) PMID: 19052340.
• Fauzdar A, Halder A *, Kumar A. Effect of gonadotropins on chromosome aneuploidy, chromosome mosaicism and skewed sex ratio in mouse preimplantation embryos. Ind J Med Res 2009; 129: 669-675. (IF 5.274; Cited by 06) PMID: 19692747.
• Halder A*. Amniotic Band Syndrome and/or Limb Body Wall Complex: Split or Lump. The Application of Clinical Genetics 2010; 3: 7-15. (IF 0.51; Cited by 37) PMID: 23776348.
• Halder A*, Jain M, Chaudhary I, Kabra M. Prevalence of 22q11.2 microdeletion in 146 patients with cardiac malformation in a referral hospital of North India. BMC Medical Genetics 2010; 11: 101. (IF 2.02; Cited by 30) PMID: 20573211.
• Halder A*, Jain M, Chaudhary I and Varma B. Chromosome 22q11.2 microdeletion in monozygotic twins with discordant phenotype and deletion size. Molecular Cytogenetics 2012; 5:13 (JIF 1.9; Cited by 51) PMID: 22413934.
• Jain M, Halder A*. Sertoli cell only syndrome: Status of sertoli cell maturation and function. Indian J Endocr Metab 2012; 16: S514-515. (IF 0.42; Cited by 18) PMID: 23565483.
• Halder A*, Jain M, Chaudhary I. Rapid Detection of Chromosome X, Y, 13, 18 & 21 Aneuploidies by Primed In Situ Labeling/Synthesis (PRINS) Technique. Ind J Hum Genet 2013; 19 (1): 14-17. (IF 0.27; Cited by 04) PMID: 2390188.
• Jain M, Mohan V, Chaudhary I, Halder A*. Sertoli cell only syndrome and glaucoma in a SRY positive XX infertile male. Journal of Clinical & Diagnostic Research 2013; 7 (7): 1457-1459. (IF 1.15; Cited by 25) PMID: 23998093.
• Halder A*, Jain M, Chaudhary I, Gupta N and Kabra M. Fluorescence in-situ hybridization (FISH) using non-commercial probes in the diagnosis of clinically suspected microdeletion syndromes: an experience with 301 cases. Ind J Med Res 2013; 138: 135-142. (IF 5.274; Cited by 24) PMID: 24056568.
• Halder A*, Jain M, Chawdhary I, Kumar G, Das TK, Gupta YK. Dark Colored Semen in Non-obstructive Azoospermia: A Report of 4 Cases. Andrologia 2014; 46: 316–321. (IF 2.53; Cited by 07) PMID: 23445433.
• Halder A*, Jain M, Kalsi AP. SNP Microarray in FISH Negative Clinically Suspected 22q11.2 Microdeletion Syndrome. Scientifica 2016; 2016:18 pages (IF 3.2; Cited by 12) PMID: 27051557.
• Jain M, Kalsi AK, Srivastava A, Gupta YK, Halder A*. High serum estradiol and heavy metals responsible for human spermiation defect. J Clin Diag and Res 2016; 10(12): RC09-RC13. (IF 1.15; Cited by 11). PMID: 28208955.
• Halder A*, Kumar P, Jain M, Iyer VK. Copy number variations in testicular maturation arrest. Andrology 2017; 5 (3): 460-472. (IF 4.45; Cited by 26) PMID: 28217865.
• Halder A*, Kumar P, Jain M, Kalsi AP. Genomics: Tool to predict & prevent male infertility. Front Biosci (Schol Ed). 2017; 9: 448-508. (IF 3.0; Cited by 17). PMID: 28410128.
• Kumar P, Jain M, Kalsi AK, Halder A*. Molecular characterization of a case of dicentric Y presented as non-obstructive azoospermia with testicular early maturation arrest. Andrologia, 2018; 50(2). (IF 2.53; Cited by 04). PMID: 28836280.
• Kalsi AK, Halder A*, Jain M, Chaturvedi PK, Sharma JB. Prevalence and Reproductive Manifestations of Macroprolactinemia. Endocrine 2019; 63(2): 332-340. (IF 3.8; Cited by 34) PMID: 30269265.
• Kalsi AK, Halder A*, Jain M, Chaturvedi PK, Mathew M, Sharma JB. Association of raised levels of IL-4 and anti-TPO with hyperprolactinemia. Am J Reproductive Immunology 2019; 81(3): e13085. (IF 3.78; Cited by 05) PMID: 30614113.
• Halder A*, Pandey D. CFTR gene variants in Indian CBAVD and its relevance in genetic counselling. Ind J Med Res 2020; 152: 535-537. (IF 5.274; Cited by 2). PMID: 34145091.
• Halder A*, Chaudhary I, Jain M. The sex ratio trajectory in mouse. Reproductive Biology 2021; 21 (3): 100514, 7 pages. (IF 2.09; Cited by 2). PMID: 34049115.
• Sharma P, Jain M, Halder A*. An investigation of steroid biosynthesis pathway genes in women with polycystic ovary syndrome. J Hum Reprod Sci 2022; 15: 240-9. (IF 1.39; Cited by 2) PMID: 36341008.
• Halder A*. Human Reproductive Genetics: Emerging Technologies and Clinical Applications. Indian J Med Res 2022; Dec 13. (IF 5.274; Cited by 1) PMID: 36510885.
• Halder A*, Kumar H, Sharma M, Jain M, Kalsi AK. Serum Anti-Müllerian hormone (AMH): most potential biomarker of PCOS from North India. Ind J Med Res 2023; 158 (4): 397-406. (IF 5.274; cited by) PMID: 37991331.
• Sharma P, Halder A*, Jain M, Tripathi M. Whole Exome Sequencing identifies rare variants in obesity- and hyperinsulinemia-related genes in PCOS. J Hum Reprod Sci 2023; 16 (4): 307-316. DOI: 10.4103/jhrs_12_23. (IF 1.39; cited by 0) PMID.

As Co-Author

• Sharma AK, Haldar A, Phadke SR, et al. Post-mortem Radiography of perinatal deaths: an aid to Genetic Counselling. Indian Pediatrics. 1994; 31(6): 702-706. (IF 3.839; Cited by 01) PMID: 7896399.
• Phadke SR, Haldhar A, Sharma AK, et al. GAPO Syndrome in a child without Dermal Hyaline Deposit. Am. J. Med. Genetics. 1994; 51: 191-193. (IF 2.578; Cited by 9) PMID: 7521121.
• Sharma AK, Haldar A, Phadke SR, et al. Preaxial Brachydactyly with Abduction of Thumbs & Hallux Varus: a distinct entity. Am. J. Med. Genetics. 1994; 49(3): 274-277. PMID: 8209885 (IF 2.578; Cited 05) PMID: 8209885.
• Sharma AK, Haldar A, Phadke SR, et al. Marshall-Smith Syndrome: further observations. Indian Pediatrics. 1994; 31(8): 1098-1100. (IF 3.839; Cited by 09) PMID: 7883370.
• Sharma AK, Phadke SR, Haldar A, et al. Jarcho-Levin Syndrome: a case report. Indian Pediatrics. 1994; 31(6): 707-708. (IF 3.839; Cited by 07) PMID: 7896400.
• Tutschek B, Sherlock J, Halder A, Delhanty J, Rodeck C, Adinolfi M. Isolation of Fetal Cells from transcervical samples by Micromanipulation: Molecular confirmation of their fetal origin and diagnosis of fetal aneuploidies. Prenatal Diagnosis. 1995; 15(10): 951-960. (IF 3.242; Cited by 48) PMID: 8587863.
• Adinolfi M, Sherlock J, Tutschek B, Halder A, Delhanty J, Rodeck C. Detection of Fetal Cells in Transcervical Sample & Prenatal Diagnosis of Chromosomal abnormalities. Prenatal Diagnosis. 1995; 15(10): 943-950. (IF 3.242; Cited by 74) PMID: 8587862.
• Agarwal S, Kishore R, Halder A, et al. Outcome of pregnancy in women with Recurrent Spontaneous Abortion following Immunotherapy with Allogenic Lymphocytes. Human Reproduction. 1995; 10(9): 2280-2284. (IF 6.353; Cited by 18) PMID: 8530652.
• Kishore R, Agarwal S, Haldar A, et al. HLA sharing, Antipaternal Cytotoxic Antibodies & MLR Blocking Factors in women with Recurrent Abortions. J Obstet Gynaecol Res. 1996; 22(2): 177-183. (IF 1.7; Cited by 49) PMID: 8697349.
• Sherlock J, Halder A, Tutschek B, Rodeck C, Adinolfi M. Prenatal detection of fetal aneuploidies using transcervical cell samples. J Med Genet. 1997; 34: 302-305. (IF 5.94; Cited by 49) PMID: 9138153.
• Jauniaux E, Halder A, Partington C. A case of partial mole associated with trisomy 13. Ultrasound Obstet Gynaecol. 1998; 11(1): 62-64. (IF 8.68; Cited by 29) PMID: 9511199.
• Pahi J, Phadke SR, Halder A, Agarwal SS, et al. Does autopsy of antenataly diagnosed malformed fetuses aid genetic counseling? The National Medical Journal of India. 1998; 11(4): 169-170. (IF 0.56; Cited by 18) PMID: 9808972.
• Yadav N, Sumod K, Kumar S, Jain M, Halder A, Saxena R, Mukhopadhyay A. Therapeutic effect of bone marrow-derived liver cells in phenotypic correction of murine hemophilia A. Blood; 2009; 114: 4552-4561. (IF 20.3; Cited by 41) PMID: 19752394.
• Shukla B, Agarwal S, Suri V, Pathak P, Sharma MC, Gupta D, Sharma BS, Suri A, Halder A, Sarkar C. Assessment of 1p/19q status by fluorescence in situ hybridization assay: A comparative study in oligodendroglial, mixed oligoastrocytic and astrocytic tumors. Neurol India 2009; 57: 559-566. (IF 1.67; Cited by 16) PMID: 19934553.
• Sharma P, Gupta N, Roychowdhury M, Phadke SR, Sapra S, Halder A, Ghosh M and Kabra M. Williams-Beuren syndrome: Delineation of clinical phenotype and diagnostic utility of MLPA: Experience of 43 patients from a tertiary care centre in India. Cytogenetic and Genome Research 2015: 146 (3): 187-194. (IF 1.7; Cited by 12) PMID: 26352091.
• Sharma A, Halder A, Kaushal S, Jain M. Intra-individual genomic variation study in tissues (Blood vs. Testis) through SNPs Microarray: Case report in two idiopathic Sertoli cell only Syndrome patients (SCOS). Journal of Reproduction & Infertility 2020; 21(4):298-307. (IF 0.5; Cited by 2) PMID: 33209747.
• Jain P, Wadhwa N, Joshi MK, Jain M, Halder A, Mishra K. Cellular mesenchymal epithelial transition (C-MET) gene copy number variation in gastric adenocarcinoma: A pilot search for new marker for targeted therapy in HER-2/neu resistance. Indian J Pathol Microbiol. 2020; 63(1): 86-89. (IF 0.77; Cited by 2) PMID: 32031129.
• Jasrotia S, Gupta R, Sharma A, Halder A, Kumar L. Cytokine profile in multiple myeloma. Cytokine 2020; 136: 155271. (IF 3.93; Cited by 33) PMID: 3296474.
• Singh M, Jain M, Bose S, Halder A, Nag T, Amit Dinda A, Mohanty S. 22(R)-hydroxycholesterol for dopaminergic neuronal specification of MSCs and amelioration of Parkinsonian symptoms in rats. Cell Death Discovery. 2021;7:13-17. (IF 7.11; Cited by 06). PMID: 33454721.
• Aggarwal D, Wadhwa N, Arora T, Rajaram S, Diwaker P, Halder A, Jain M, Mishra K. Human telomerase RNA component (hTERC) gene expression and chromosome 7 ploidy correlate positively with histological grade of cervical intraepithelial neoplasia. Cytopathology. 2021;32(5):631-639. IF 1.28; Cited by 01. PMID: 33848025
• Sharma A, Jain M, Halder A, Kaushal S. Identification of Genomic imbalances (CNVs as well as LOH) in Sertoli Cell Only Syndrome cases through Cytoscan Microarray. Gene 2021;30;801:145851 (JIF 3.91; Cited by 6) PMID: 34274474.
• Kaushik N, Rastogi S, Verma S, Pandey D, Halder A, Mukhopadhyay A, Kumar N. Transcriptome analysis of insulin signaling associated transcription factors in C. elegans reveal their genome-wide target genes specificity and complexity. International Journal of Molecular Sciences 2021; 22: 12462 (JIF 5.6; Cited by 1). PMID: 34830338.
• Srinivasan P, Meena JP, Gupta AK, Halder A, Kapil A, Pandey RM, Seth R. Safety of Procalcitonin Guided Early Discontinuation of Antibiotic Therapy among Children Receiving Cancer Chemotherapy and Having Low-Risk Febrile Neutropenia: A Randomized Feasibility Trial (ProFenC Study). Pediatr Hematol Oncol. 2023 Sep 1:1-14. doi: 10.1080/08880018.2023.2249940. PMID: 37655541. (JIF 1.17; Cited by 0)
• Sharma M, Sharma Y, Halder A, Mahey R; Kumar N. Effect of human sperm vitrification on phospholipase c ζ expression. Cryobiology (2023; submitted)

Other (non-PubMed) Journals
As First/Corresponding Author

• Halder A*. Trisomy 21 beyond 1st trimester: are they all mosaic? Evidence to support. Asian J Obs & Gynae Practice, 2002; 6 (2): 30-34. (IF NA; Cited by 01)
• Halder A*, Agarwal S & Chaddha V. Genetic counseling in obstetric practice. Obstetrics & Gynecology Today 2002; VII (6): 310-318 (IF NA; Cited by 01).
• Agarwal S, Chadda V, Ram Sharan, Halder A*. Rapid prenatal diagnosis of trisomy 18 by interphase FISH. Asian Journal of Obs & Gynae Practice 2003; 7 (1): 14–15 & 23. (IF NA; Cited 03)
• Halder A*, Halder S, Fauzdar A, Kumar A. Molecular approaches of chromosome analysis: an overview. Proc. Indian Nat. Sci. Acad. 2004; B70 (2): 153-221. (IF NA; Cited by 05)
• Halder A*. Placental chimerism in early human pregnancy. Ind J of Hum Genet 2005; 11 (2): 84-88. (IF 0.27; Cited by 05)
• Halder A*. Premature greying of hairs, premature ageing and predisposition to cancer in Jajjal, Punjab: a preliminary observation. Journal of Clinical & Diagnostic Research 2007; 6: 577-580 (IF 1.15; Cited by 25)
• Halder A*, Gupta RK. Male like external genitalia with epididymis in a case of 46,XX disorder of sex development due to congenital adrenal hyperplasia. Journal of Research in Medical Sciences 2008; 13(3): 141-145. (IF 1.6; Cited by 02)
• Halder A*. 46, XY Disorder of Sex Development with Mullerian Ducts Remnants. Journal of Clinical & Diagnostic Research 2010; 4: 2169-2174 (IF 1.15; Cited by 04)
• Halder A*. Advances in Cytogenetics (editorial). JBR Journal of Clinical Diagnosis and Research. 2013; 16:e101.doi:10.4172/jcdr.1000e101 Volume1 Issue1 1000e101. (IF 0.845; Cited by 03)
• Halder A*. Disorder of Sex Development: spectrum of disorder in a referral tertiary care hospital in Northern India. The Global Journal of Human Genetics & Gene Therapy. 2013; 1 (2): 77-89 (IF NA; Cited by 05)
• Halder A*. Cytogenetics to Cytogenomics: transition from Chromosome to DNA sequence. The Global Journal of Human Genetics & Gene Therapy. 2013; 1 (2): 90-104 (IF NA; Cited by 3)
• Halder A*. Lethal Developmental Defects: An Overview. Open Journal of Obstetrics and Gynecology 2014; 4: 1006-1036 (IF 0.59; Cited by 03)
• Chaudhary I, Jain M, Halder A*. Sperm sex ratio (X:Y ratio) and its variations. Austin J Reprod Med Infertil. 2014;1(1): 7 (arjm-v1-id1003) (IF 1.9; Cited by 68)
• Halder A*. Canceromics and P3 medicine (editorial). JBR J Clin Diagn Res 2015; 3: 1 (1000e104). 2 pages (IF 0.845; Cited by 01)
• Halder A*, Jain M and Kumar P. Primary Testicular Failure: An Overview. JBR J Clin Diagn Res 2015; 3: 1 (1000e105). 5 pages (IF 0.845; Cited by 08)
• Halder A*. Reproductive Genetic Counselling in Genomic Era. EC Gynaecology 2015; 2 (1): 132-148. (IF 1.6; Cited by 04)
• Halder A*. Reproductive Genetics (editorial). JBR Journal of Clinical Diagnosis and Research 2016; 4: 106 (2 pages). (IF 0.845; Cited by 02)
• Halder A*. Approach to Prenatal Fetal Malformations. EC Gynaecology 2016; 3 (3): 294-307. (IF 1.6; Cited by 02)
• Halder A*. Non-invasive Prenatal Testing. EC Gynaecology 2016; 3 (5): 365-367. (IF 1.6; Cited 0)
• Jain M, Kalsi AK, Srivastava A, Gupta YK, Halder A*. High serum estradiol and heavy metals responsible for human spermiation defect. J Clin Diag and Res 2016; 10(12): RC09-RC13. (IF 1.15; Cited by 11).
• Halder A*, Jain M, Kalsi APK. Mosaicism in 22q11.2 Microdeletion Syndrome. J Clin Diagn Res. 2018; 12: 1-6 (IF 1.15; Cited by 05)
• Kalsi AK, Halder A*, Jain M, Srivastava A (corresponding author). Association of Cadmium, Chromium, Manganese and Lead with hyperprolactinemia. Journal of Clinical and Diagnostic Research 2020; 14: 4-7. (IF 1.15; Cited by 0)
• Halder A*, Kumar H. “Polycystic Ovary Syndrome (PCOS): The Pros and Cons of Various Diagnostic Criteria”. EC Gynaecology 2020; 9(12): 39-41. (IF 1.6; Cited by 03)
• Rana R, Mohanty S, Halder A*. Salient Yet Silent: A Need for Strategies to Cope with Violence against Infertile Women during COVID-19 Pandemic. EC Gynaecology 2021;10(1):29-31. (IF 1.16; Cited by 1)
• Kalsi AK, Jain M, Halder A*. An investigation on bone mineral density in hyperprolactinemia. Journal Endocrinology and Reproduction 2020; 24 (2): 107-121. (IF 1.05; Cited by 1).
• Kumar H, Halder A*, Sharma M, Kalsi AK, Jain M. Dihydrotestosterone: a potential biomarker of hyperandrogenaemia in PCOS. J Clin and Diag Res 2022; 16(2): QC09-QC14. (JIF 1.15; Cited by 03).
• Rana R, Sharma M, Halder A*. New insights into the mechanism of pathogenesis of fragile X-associated premature ovarian failure. EC Gynecology 2022; 11.7 (6 pages) (IF 1.16; Cited by 1)
• Halder A*, Kumar H, Sharma P, Sharma M, Jain M. Polycystic Ovary Syndrome (PCOS): An Overview and our experience. Journal of Endocrinology and Reproduction 2022; 26 (3): 127-152. (IF 1.05; Cited by 2)
• Halder A*, Sharma P, Rana R, Jain M, Sharma M. The Genetic and Genomic Landscape of Human Reproductive Disorders: An Overview with Our Experience. Med Res Arch 2023; 11 (3): 1-36. IF: NA; Cited by 0).
• Sharma P, Jain M, Tripathi M, Sharma M, Halder A*. An update on the genetics of polycystic ovary syndrome. Journal of Endocrinology and Reproduction 2023;27(4):217-240. (DOI: 10.18311/jer/2023/34654)
• Sharma P, Jain M, Halder A*. Comprehensive chromosomal screening for preimplantation genetic testing (PGT): A mini-review. Fertility Science Research 2023;10(4): 188-94.
• Kalsi AK, Halder A*, Jain M. Epigenetics in Etiopathology of Hyperprolactinemia. Exploration of Endocrine and Metabolic Disease (EEMD-2023-00007) 2024;2(1): pp (accepted; in a special issue on "The HPA Axis in Health and Disease”)
• Halder A*, Kumar N. Editorial: Endometriosis. What do we know about etiology? EC Gynae 2024 (sub)

As Co-Author

• Buckshee K, Haldar A, et al. Bioeffects of Diagnostic Ultrasound in Newborn. J. Obst. & Gynecol India. 1994; 44(1): 859-862. (IF 0.87; Cited by 0)
• Ruangvutilert P, Halder A, Jauniaux E, Arienzo M, Cirigliano V and Sherlock J. A minimally invasive prenatal diagnosis technique for the collection of transcervical cells. Prenatal Neonatal Medicine 1998; 3: 294 - 296. (IF 0.54; Cited by 06)
• Phadke SR, Halder A. Fluorescent in situ hybridization: A novel method to study chromosomes and genes. Perinatology 2000; 2(4): 203-210. (IF NA; Cited by NA)
• Pandey MK, Halder A, Agarwal S, Srivastava M, Agarwal SS, Agrawal S. Immunotherapy in Recurrent Spontaneous Abortion: Randomised and Nonrandomised trials. The Internet Journal of Gynaecology and Obstetrics 2003; 2(1): rsa/xml (13 pages). (IF 0.33; Cited 17)
• Nagpure NS, Kushwaha B, Srivastava SK, Halder A, Ponniah AG. Comparative chromosome painting in fish using human sex chromosome probes. Indian J Fishery 2003; 50: 103-106. (IF 0.59; Cited by 03)
• Kumar A, Halder A, Mohanty BP, Kumar G, Rani L. Clinical trial of Ashokarishta, a phytoestrogen in postmenopausal women: A pilot study. Indian Journal of Endocrinology and Metabolism. 2009;13(2):24-30. (IF 0.425; Cited by 0)
• Rishi I, Halder A, Sharma JB, Jain M, Sharma M. Single Strand Conformation Polymorphism and Sequencing of HS6ST2 Gene in Patients of Idiopathic Premature Ovarian Failure. Journal of Clinical and Diagnostic Research. 2020; 14(2): GC01-GC08 (IF 1.15; Cited by 03)
• Joginder, Halder A, Sharma JB, Mahey R, Gupta S, Sharma M. A preliminary study of human sperm citrate synthase expression in patients with failed ICSI cycles. Journal of Research in Biology 2020; 10: 2888-2897. (IF NA; Cited by 0)
• Sharma M, Halder A. Understanding Basic Concepts of Premature Ovarian Failure. EC Gynaecology 2021; 10 (11): 25-36. (IF 1.16; Cited by 3)
• Kumar H, Halder A, Sharma M. Bisphenol and PCOS: Does the link exist? ReproGenQ 2021;3(Apr):13-16. (IF 0; Cited by 0)
• Rana R, Halder A, Gupta S, Sharma M. An in-vitro analysis of L-Carnitine mediated rescue of TNF-α induced apoptosis in mice oocytes. Int J Clin Biochem Res 2022;9(3):218-223. (IF 1.2; Cited by 0)
• Halder A, Halder A, Nishad AK. Music in Medicine: An overview. Ind J Clin Anes. 2023; 10 (1): 01-10. (IF 0.53; Cited by 0)
• Sharma M, Sihag K, Halder A, Sharma JB. Premature ovarian insufficiency in adolescents. Indian Obstetrics & Gynaecology 2023;13(3):45-49. (IF 0; Cited by 0)
• Sharma N, Halder A, Kaushal S, Kumar M, Jain M. Next generation sequencing based exploration of potential candidate variants and microRNAs in patients with idiopathic Hypospermatogenesis sub-type of Non-Obstructive Azoozpermia. Research Square 2023. DOI: https://doi.org/10.21203/rs.3.rs-3427200/v1.