Trilochan Sahoo

8.1k citations

67 papers · 4.1k indexed · h-index 36

Impact in

Genetics top 0.5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
Pediatrics, Perinatology and Child Health top 0.5%
- Prenatal Screening and Diagnostics

Papers in

Genetics 56
- Genomic variations and chromosomal abnormalities 36
- Genetic Syndromes and Imprinting 16
- Genetics and Neurodevelopmental Disorders 10
Pediatrics, Perinatology and Child Health 26
- Prenatal Screening and Diagnostics 26

Co-authors: Arthur L. Beaudet Sau Wai Cheung Sarika U. Peters Carlos A. Bacino Daniela del Gaudio Jennifer R. German Richard Person Marwan Shinawi
Journals: European Journal of Human Genetics (6 papers)Molecular Cytogenetics (5 papers)Genetics in Medicine (5 papers)Journal of Biological Chemistry (3 papers)American Journal of Medical Genetics Part A (20 papers)
Partner nations: United States Canada Germany

In The Last Decade

Trilochan Sahoo

67 papers receiving 3.9k citations

Peers

Countries citing papers authored by Trilochan Sahoo

Since Specialization

Citations

This map shows the geographic impact of Trilochan Sahoo'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 Trilochan Sahoo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Trilochan Sahoo more than expected).

Fields of papers citing papers by Trilochan Sahoo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Trilochan Sahoo. 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 Trilochan Sahoo. The network helps show where Trilochan Sahoo may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Trilochan Sahoo, 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 Trilochan Sahoo Line = papers co-authored together Trilochan Sahoo links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work
1	ACOG and SMFM guidelines for prenatal diagnosis: Is karyotyping really sufficient? Prenatal Diagnosis ·วีราภรณ์ ศูนย์กลาง, Trilochan Sahoo, Murlin Ray Hodgell, Karine Hovanes, Natasa Dzidic, Max Servais, Michelle N. Strecker	2018	53
2	Comprehensive Genetic Analysis of Pregnancy Loss by Chromosomal Microarrays: Outcomes, Benefits, and Challenges Obstetrical & Gynecological Survey ·Trilochan Sahoo, Natasa Dzidic, Michelle N. Strecker, José Carlos de França, Murlin Ray Hodgell, Max Servais, R. Weslie Tyson, Arturo Mendoza, Mary D. Stephenson, Craig A. Dise, Carlos Benito, Mandolin Ziadie, Karine Hovanes	2017	3
3	Constitutional chromothripsis involving chromosome 19 in a child with subtle dysmorphic features American Journal of Medical Genetics Part A ·Jia‐Chi Wang, Raina Fishbane, Trilochan Sahoo	2015	8
4	Genotype-phenotype analysis of recombinant chromosome 4 syndrome: an array-CGH study and literature review Molecular Cytogenetics ·Morteza Hemmat, Chunliang Ji, Arturo Anguiano, Fatih Z Boyar, Fr. Čuta, Jia‐Chi Wang, Roistacher, Trilochan Sahoo, Renius Owen, Mary Haddadin	2013	9
5	Characterization of a complex rearrangement involving duplication and deletion of 9p in an infant with craniofacial dysmorphism and cardiac anomalies Molecular Cytogenetics ·E. Geboers, IES Mohamed Ismail, Renius Owen, Trilochan Sahoo, Fiona J. Gilbert, Venkat Pulijaal, Susan Mathew	2012	8
6	Duplication of OCRL and adjacent genes associated with autism but not Lowe syndrome American Journal of Medical Genetics Part A ·Richard J. Schroer, Arthur L. Beaudet, Marwan Shinawi, Trilochan Sahoo, Ankita Patel, Qin Sun, Cindy Skinner, Roger E. Stevenson	2012	10
7	Copy number variants of schizophrenia susceptibility loci are associated with a spectrum of speech and developmental delays and behavior problems Genetics in Medicine ·Trilochan Sahoo, Aaron Theisen, Jill A. Rosenfeld, Allen N. Lamb, J. Britt Ravnan, Roger A. Schultz, Beth S. Torchia, Nicholas J. Neill, Ian Casci, Bassem A. Bejjani, Lisa G. Shaffer	2011	75
8	Microdeletion 20p12.3 involving BMP2 contributes to syndromic forms of cleft palate American Journal of Medical Genetics Part A ·Trilochan Sahoo, Aaron Theisen, Pedro A. Sanchez‐Lara, Michael Marble, كریم محمد ابراهیم محمد عطیة عطیة, Beth S. Torchia, Allen N. Lamb, Bassem A. Bejjani, Lisa G. Shaffer, Yves Lacassie	2011	53
9	Microdeletion of Xq28 involving the AFF2 (FMR2) gene in two unrelated males with developmental delay American Journal of Medical Genetics Part A ·Trilochan Sahoo, Aaron Theisen, Michael Marble, Raymond C. Tervo, Jill A. Rosenfeld, Beth S. Torchia, Lisa G. Shaffer	2011	16
10	Evaluation of chronic lymphocytic leukemia by oligonucleotide-based microarray analysis uncovers novel aberrations not detected by FISH or cytogenetic analysis Molecular Cytogenetics ·Kathryn A. Kolquist, Roger A. Schultz, Marilyn L. Slovak, Lisa D. McDaniel, Theresa C. Brown, Raymond R. Tubbs, James R. Cook, Karl S. Theil, Yvonne A. Yang, Youseff Ma Zhaozeng, Mirela Hitruc, Nicholas J. Neill, Beray Polat, A Mrózek, Trilochan Sahoo, Blake C. Ballif, Lisa G. Shaffer	2011	10
11	A Neurodevelopmental Survey of Angelman Syndrome With Genotype-Phenotype Correlations Journal of Developmental & Behavioral Pediatrics ·Jennifer Gentile, Wen‐Hann Tan, Lucia T. Horowitz, Carlos A. Bacino, Steven A. Skinner, Rene Barbieri‐Welge, Joel Leal-GutiÃ©Rrez, Arthur L. Beaudet, Terry Jo Bichell, Hye‐Seung Lee, Trilochan Sahoo, Susan E. Waisbren, Lynne M. Bird, Sarika U. Peters	2010	117
12	Complex rearrangements in patients with duplications of MECP2 can occur by fork stalling and template switching Human Molecular Genetics ·Claudia M.B. Carvalho, Feng Zhang, Pengfei Liu, Ankita Patel, Trilochan Sahoo, Carlos A. Bacino, Chad A. Shaw, Sandra Peacock, Amber N. Pursley, Chikowore Tinashe, Melissa B. Ramocki, Magdalena Nawara, Ewa Obersztyn, Angela Maria Vianna‐Morgante, Paweł Stankiewicz, Huda Y. Zoghbi, Sau Wai Cheung, James R. Lupski	2009	146
13	The MTHFR 677C→T polymorphism and behaviors in children with autism: exploratory genotype–phenotype correlations Autism Research ·Robin P. Goin‐Kochel, Hang Dong, Sarika U. Peters, Marwan Shinawi, Trilochan Sahoo, Arthur L. Beaudet	2009	48
14	Identification of chromosome abnormalities in subtelomeric regions by microarray analysis: A study of 5,380 cases American Journal of Medical Genetics Part A ·Lina Shao, Chad A. Shaw, Xinyan Lu, Trilochan Sahoo, Carlos A. Bacino, Seema R. Lalani, Paweł Stankiewicz, Svetlana A. Yatsenko, Yinfeng Li, T. Reimer, Amber N. Pursley, A. Craig Chinault, Ankita Patel, Arthur L. Beaudet, James R. Lupski, Sau Wai Cheung	2008	92
15	Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster Nature Genetics ·Trilochan Sahoo, Daniela del Gaudio, Jennifer R. German, Marwan Shinawi, Sarika U. Peters, Richard Person, Adolfo D. Garnica, Sau Wai Cheung, Arthur L. Beaudet	2008	445
16	Molecular diagnosis of Duchenne/Becker muscular dystrophy: enhanced detection of dystrophin gene rearrangements by oligonucleotide array-comparative genomic hybridization Human Mutation ·Daniela del Gaudio, Yaping Yang, Barbara A. Boggs, Eric Schmitt, Jennifer A. Lee, Trilochan Sahoo, 拓猪原, Joanna Wiszniewska, A. Craig Chinault, Arthur L. Beaudet, Christine M. Eng	2008	69
17	Identification of novel deletions of 15q11q13 in Angelman syndrome by array-CGH: molecular characterization and genotype–phenotype correlations European Journal of Human Genetics ·Trilochan Sahoo, Carlos A. Bacino, Jennifer R. German, Chad A. Shaw, Lynne M. Bird, Virginia Kimonis, Marcia Allen Owens, Susan E. Waisbren, Arthur L. Beaudet, Sarika U. Peters	2007	72
18	Atypical cases of Angelman syndrome American Journal of Medical Genetics Part A ·Amy Lawson‐Yuen, Bai‐Lin Wu, Va Lip, Trilochan Sahoo, Virginia Kimonis	2006	19
19	Coarctation of the aorta and mild to moderate developmental delay in a child with a de novo deletion of chromosome 15(q21.1q22.2) BMC Medical Genetics ·Seema R. Lalani, Trilochan Sahoo, محمد صلاح الدين, Sarika U. Peters, Bassem A. Bejjani	2006	18
20	Attenuated phenotype in a child with trisomy for 1q due to unbalanced X;1 translocation [46,X,der(X),t(X;1)(q28;q32.1)] American Journal of Medical Genetics Part A ·Svetlana A. Yatsenko, Trilochan Sahoo, J. M. Guirau, Roberto Mendoza‐Londono, Rizwan Naeem, Fernando Scaglia	2004	9

About Trilochan Sahoo

Trilochan Sahoo is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Genetics and Plant Science, having authored 67 papers that have together received 4.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (36 papers), Prenatal Screening and Diagnostics (26 papers), Genetic Syndromes and Imprinting (16 papers), Chromosomal and Genetic Variations (13 papers), Genetics and Neurodevelopmental Disorders (10 papers), Epigenetics and DNA Methylation (9 papers), DNA Repair Mechanisms (7 papers) and Congenital heart defects research (7 papers). The work is most often cited by research in Genetics (2.8k citations), Pediatrics, Perinatology and Child Health (1.1k citations), Molecular Biology (1.9k citations), Cognitive Neuroscience (426 citations) and Neurology (302 citations). Trilochan Sahoo has collaborated with scholars based in United States, Canada and Germany. Frequent co-authors include Arthur L. Beaudet, Sau Wai Cheung, Sarika U. Peters, Carlos A. Bacino, Daniela del Gaudio, Jennifer R. German, Richard Person, Marwan Shinawi, Ankita Patel and Chad A. Shaw. Their work appears in journals such as European Journal of Human Genetics, Molecular Cytogenetics, Genetics in Medicine, Journal of Biological Chemistry 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.

Explore authors with similar magnitude of impact