B. A. Bharucha

492 citations

41 papers · 251 indexed · h-index 9

Impact in

Developmental Biology
Genetics
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Connective tissue disorders research
- Genetic Syndromes and Imprinting

Papers in

Developmental Biology 4
- Congenital limb and hand anomalies 4
Genetics 15
- Genomic variations and chromosomal abnormalities 4
- Craniofacial Disorders and Treatments 4
- Connective tissue disorders research 3
- Genetic and rare skin diseases. 2

Co-authors: Mamta Muranjan Milind S. Tullu C T Deshmukh Arijit Chattopadhyay Seema Sharma Pankaj Arora Anupam Chakrapani N A Kshirsagar
Journals: The Indian Journal of Pediatrics (14 papers)Annals of Plastic Surgery (1 paper)Pediatric Neurosurgery (1 paper)Clinical Dysmorphology (2 papers)American Journal of Medical Genetics Part A (1 paper)
Partner nations: India Australia United Kingdom

In The Last Decade

B. A. Bharucha

40 papers receiving 225 citations

Peers

Countries citing papers authored by B. A. Bharucha

Since Specialization

Citations

This map shows the geographic impact of B. A. Bharucha's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by B. A. Bharucha with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites B. A. Bharucha more than expected).

Fields of papers citing papers by B. A. Bharucha

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by B. A. Bharucha. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by B. A. Bharucha. The network helps show where B. A. Bharucha may publish in the future.

Co-authorship network

The 24 scholars most cited alongside B. A. Bharucha, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with B. A. Bharucha Line = papers co-authored together B. A. Bharucha links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Congenital and inherited ophthalmologic abnormalities The Indian Journal of Pediatrics ·Львов А.Е., Milind S. Tullu, Mamta Muranjan, 李輝煌, Katta M. Girisha, B. A. Bharucha	2003	3
2	Ring chromosome 12 with variable phenotypic features: Clinical report and review of the literature American Journal of Medical Genetics Part A ·佳也楠, Mamta Muranjan, J. Kalaivani Sailaja, Seema Sharma, B. A. Bharucha	2003	19
3	Ovarian dysgenesis with balanced autosomal translocation. PubMed ·Milind S. Tullu, Pankaj Arora, K. Pema, Aimee Atikah Zakaria, B. A. Bharucha	2002	16
4	Ovarian dysgenesis with balanced autosomal translocation. SHILAP Revista de lepidopterología ·Milind S. Tullu, Pankaj Arora, 佳也楠, Mamta Muranjan, B. A. Bharucha	2001	0
5	Autosomal dominant ectrodactyly with sensorineural deafness Clinical Dysmorphology ·J. V. Meegoda, Mamta Muranjan, B. A. Bharucha	2000	2
6	Superior sagittal sinus thrombosis: a rare complication of nephrotic syndrome. PubMed ·Milind S. Tullu, Avilla Deva Aryanda, Robin Ytterlid, Amir Safaeinasab, B. A. Bharucha	2000	8
7	Dorfman-Chanarin syndrome: a rare neutral lipid storage disease. PubMed ·Milind S. Tullu, Mamta Muranjan, Jiawei Wu, C T Deshmukh, Dae-Su Kyung, B. A. Bharucha	2000	11
8	Osteoporosis pseudoglioma syndrome. PubMed ·Erica Elice Lessa Ferreira, Kim M. Davis, Priyanka Mishra, Mamta Muranjan, B. A. Bharucha	1999	8
9	Familial glucocorticoid deficiency, alacrimia and achalasia—Allgrove syndrome The Indian Journal of Pediatrics ·Mamta Muranjan, Mary K. Ferneau, Yoshikazu Ajisawa, C T Deshmukh, B. A. Bharucha	1999	2
10	Supernumerary Limbs: A Case Report of a Rare Congenital Anomaly Annals of Plastic Surgery ·Hyun Sang Won, Edgar Mauricio Medina Tovar, 강안종, Talissa B. C. Lopes, Arseniy Vitkovksiy, B. A. Bharucha, Belinda Gowen	1996	6
11	Familial Congenital Valvar Pulmonary Stenosis: Autosomal Dominant Inheritance Pediatric Cardiology ·Arooj Mir, Sachin Khambadkone, B. A. Bharucha, Yash Lokhandwala, Michael D. Sklar	1996	4
12	Craniosynostosis and Klippel-Feil syndrome : A rare association The Indian Journal of Pediatrics ·Arijit Chattopadhyay, Ashish Shah, Byoung-Yeol Choi, B. A. Bharucha, A. Yaffe	1996	3
13	Klippel-Trenaunay-Weber Syndrome with Hydrocephalus: An Unusual Association Pediatric Neurosurgery ·Girish Gupte, Edwin Gérman Maldonado Távara, B. A. Bharucha, Michael D. Sklar	1995	3
14	Mucolipidoses—II: a report of three cases The Indian Journal of Pediatrics ·Estefanía Atehortúa Uribe, Byoung-Yeol Choi, Anne Olsen, B. A. Bharucha, AN Tenriawaru	1995	2
15	Neurofibromatosis presenting with aqueductal stenosis The Indian Journal of Pediatrics ·Arijit Chattopadhyay, Hyun Sang Won, Joan Majó Roca, C T Deshmukh, B. A. Bharucha	1994	1
16	Acrodysostosis with 5α reductase deficiency: An unsual association The Indian Journal of Pediatrics ·Girish Gupte, Hyun Sang Won, Henry J. Sustakoski, B. A. Bharucha, E Brähler	1994	2
17	Spondylocostal dysostosis The Indian Journal of Pediatrics ·Hyun Sang Won, Matthias Friedrich Albiez, Muñoz Sacristán, Sachin Khambadkone, B. A. Bharucha, BİLAL KARACA	1993	4
18	Deletion of short-arm of chromosome 20:46 XX, del (20) (p 11) with unusual skeletal features The Indian Journal of Pediatrics ·XuTingQiao, B. A. Bharucha, Marilys de Jesus, C C Steevens, Hyun Sang Won, Paul Schmiedmayer	1991	10
19	The mucopolysaccharidoses: A study of 48 cases The Indian Journal of Pediatrics ·シャラートヴァデーラ, B. A. Bharucha, Theodore Levin, AN Tenriawaru	1988	6
20	Siblings with the Austin variant of metachromatic leukodystrophy multiple sulfatidosis The Indian Journal of Pediatrics ·B. A. Bharucha, AN Tenriawaru, PY Carry, Ravi Joshi, Theodore Levin	1984	7

About B. A. Bharucha

B. A. Bharucha is a scholar working on Developmental Biology, Genetics, Clinical Biochemistry, Biochemistry and Epidemiology, having authored 41 papers that have together received 251 indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (5 papers), Congenital limb and hand anomalies (4 papers), Hedgehog Signaling Pathway Studies (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Craniofacial Disorders and Treatments (4 papers), Connective tissue disorders research (3 papers), Trypanosoma species research and implications (3 papers) and Genetic and rare skin diseases. (2 papers). The work is most often cited by research in Developmental Biology (11 citations), Genetics (106 citations), Pediatrics, Perinatology and Child Health (58 citations), Biochemistry (14 citations) and Urology (11 citations). B. A. Bharucha has collaborated with scholars based in India, Australia and United Kingdom. Frequent co-authors include Mamta Muranjan, Milind S. Tullu, C T Deshmukh, Arijit Chattopadhyay, Seema Sharma, Pankaj Arora, Anupam Chakrapani, N A Kshirsagar, Priyanka Mishra and Suhag Parikh. Their work appears in journals such as The Indian Journal of Pediatrics, Annals of Plastic Surgery, Pediatric Neurosurgery, Clinical Dysmorphology and American Journal of Medical Genetics Part A.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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