Trilochan Sahoo

8.1k citations

67 papers · 4.2k · h-index 36

Impact in

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

Papers in

Genetics 50
- Genomic variations and chromosomal abnormalities 29
- Genetic Syndromes and Imprinting 16
- Genetics and Neurodevelopmental Disorders 8
- Bacterial Genetics and Biotechnology 7
Molecular Biology 25
- DNA Repair Mechanisms 7
- Epigenetics and DNA Methylation 7

Co-authors: Arthur L. Beaudet (21 shared papers)Sau Wai Cheung (14 shared papers)Sarika U. Peters (12 shared papers)Daniela del Gaudio (6 shared papers)Carlos A. Bacino (13 shared papers)Jennifer R. German (4 shared papers)Ankita Patel (12 shared papers)Richard Person (2 shared papers)
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 (21 papers)
Partner nations: United States Canada Germany

In The Last Decade

Trilochan Sahoo

67 papers receiving 4.0k 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-authors

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

Showing the 20 most-cited of 67 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	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	446
2	Mutations in the Gene Encoding KRIT1, a Krev-1/rap1a Binding Protein, Cause Cerebral Cavernous Malformations (CCM1) Human Molecular Genetics ·Trilochan Sahoo, Eric W. Johnson, James W. Thomas, Peter Kuehl, Tamara L. Jones, C. G. Dokken, Jeffrey W. Touchman, Carol J. Gallione, S.-Q. Lee-Lin, Barry E. Kosofsky, Janice Kurth, David N. Louis, Gabrielle Mettler, Leslie Morrison, António Gil‐Nagel, Stephen S. Rich, Joseph M. Zabramski, Mark S. Boguski, Eric D. Green, Douglas A. Marchuk	1999	290
3	Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader–Willi syndrome European Journal of Human Genetics ·Angela L. Duker, Blake C. Ballif, Erawati V. Bawle, Richard Person, Sangeetha Mahadevan, Sarah Alliman, Regina Thompson, Ryan N. Traylor, Bassem A. Bejjani, Lisa G. Shaffer, Jill A. Rosenfeld, Allen N. Lamb, Trilochan Sahoo	2010	237
4	Clinical Implementation of Chromosomal Microarray Analysis: Summary of 2513 Postnatal Cases PLoS ONE ·Xinyan Lu, Chad A. Shaw, Ankita Patel, Jiangzhen Li, M. Lance Cooper, William R. Wells, Cathy Sullivan, Trilochan Sahoo, Svetlana A. Yatsenko, Carlos A. Bacino, Paweł Stankiewicz, Zhishu Ou, A. Craig Chinault, Arthur L. Beaudet, James R. Lupski, Sau Wai Cheung, Patricia A. Ward	2007	148
5	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, Y. Jane Tavyev, Melissa B. Ramocki, Magdalena Nawara, Ewa Obersztyn, Angela Maria Vianna‐Morgante, Paweł Stankiewicz, Huda Y. Zoghbi, Sau Wai Cheung, James R. Lupski	2009	146
6	Microarray‐based CGH detects chromosomal mosaicism not revealed by conventional cytogenetics American Journal of Medical Genetics Part A ·Sau Wai Cheung, Chad A. Shaw, Daryl A. Scott, Ankita Patel, Trilochan Sahoo, Carlos A. Bacino, Amber N. Pursley, Jiangzhen Li, Robert P. Erickson, Andrea Gropman, David T. Miller, Margretta R. Seashore, Anne Summers, Paweł Stankiewicz, A. Craig Chinault, James R. Lupski, Arthur L. Beaudet, V. Reid Sutton	2007	140
7	Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization Genetics in Medicine ·Trilochan Sahoo, Sau Wai Cheung, Patricia A. Ward, Sandra Darilek, Ankita Patel, Daniela del Gaudio, Sung Hae L. Kang, Seema R. Lalani, Jiangzhen Li, Sallie McAdoo, Audrey Burke, Chad A. Shaw, Paweł Stankiewicz, A. Craig Chinault, Ignatia B. Van den Veyver, Benjamin B. Roa, Arthur L. Beaudet, Christine M. Eng	2006	128
8	Comprehensive genetic analysis of pregnancy loss by chromosomal microarrays: outcomes, benefits, and challenges Genetics in Medicine ·Trilochan Sahoo, Natasa Dzidic, Michelle N. Strecker, Sara Commander, Mary K. Travis, Charles Doherty, R. Weslie Tyson, Arturo Mendoza, Mary D. Stephenson, Craig A. Dise, Carlos Benito, Mandolin Ziadie, Karine Hovanes	2016	123
9	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, Astrid Bauer‐Carlin, Arthur L. Beaudet, Terry Jo Bichell, Hye‐Seung Lee, Trilochan Sahoo, Susan E. Waisbren, Lynne M. Bird, Sarika U. Peters	2010	120
10	A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3A American Journal of Medical Genetics Part A ·Yong‐hui Jiang, Trilochan Sahoo, Ron C. Michaelis, Dani Bercovich, Jan Bressler, Catherine D. Kashork, Qian Liu, Lisa G. Shaffer, Richard J. Schroer, David W. Stockton, Richard S. Spielman, Roger E. Stevenson, Arthur L. Beaudet	2004	113
11	Cerebral folate deficiency with developmental delay, autism, and response to folinic acid Neurology ·Paolo Moretti, Trilochan Sahoo, Κ. Hyland, Teodoro Bottiglieri, Sarika U. Peters, Daniela del Gaudio, B. Roa, Stephen H. Curry, Hengyue Zhu, Richard H. Finnell, Jeffrey L. Neul, V. Ramaekers, Nenad Blau, Carlos A. Bacino, G. Miller, Fernando Scaglia	2005	108
12	Genomic Imbalances in Neonates With Birth Defects: High Detection Rates by Using Chromosomal Microarray Analysis PEDIATRICS ·Xin-Yan Lu, My Thao Phung, Chad A. Shaw, Kim Pham, Sarah Neil‐Sztramko, Ankita Patel, Trilochan Sahoo, Carlos A. Bacino, Paweł Stankiewicz, Sung-Hae L. Kang, Seema R. Lalani, A. Craig Chinault, James R. Lupski, Sau Wai Cheung, Arthur L. Beaudet	2008	105
13	Clinical spectrum associated with recurrent genomic rearrangements in chromosome 17q12 European Journal of Human Genetics ·Sandesh C. Sreenath Nagamani, Ayelet Erez, Joseph Shen, Chumei Li, Elizabeth Roeder, Sarah K. Cox, Lefkothea Karaviti, Margret Pearson, Sung‐Hae Kang, Trilochan Sahoo, Seema R. Lalani, Paweł Stankiewicz, V. Reid Sutton, Sau Wai Cheung	2009	103
14	22q13.3 deletion syndrome: Clinical and molecular analysis using array CGH American Journal of Medical Genetics Part A ·Shweta U. Dhar, Daniela del Gaudio, Jennifer R. German, Sarika U. Peters, Zhishu Ou, Patricia I. Bader, Jonathan S. Berg, Maria Blazo, Chester Brown, Brett H. Graham, Theresa A. Grebe, Seema R. Lalani, Mira Irons, Steven Sparagana, Melissa Williams, (unknown), Arthur L. Beaudet, Paweł Stankiewicz, Ankita Patel, Sau Wai Cheung, Trilochan Sahoo	2010	98
15	Copy number variations associated with autism spectrum disorders contribute to a spectrum of neurodevelopmental disorders Genetics in Medicine ·Jill A. Rosenfeld, Blake C. Ballif, Beth S. Torchia, Trilochan Sahoo, J. Britt Ravnan, Roger A. Schultz, Allen N. Lamb, Bassem A. Bejjani, Lisa G. Shaffer	2010	94
16	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, Sarah E. Neill, Amber N. Pursley, A. Craig Chinault, Ankita Patel, Arthur L. Beaudet, James R. Lupski, Sau Wai Cheung	2008	93
17	Angelman syndrome: Mutations influence features in early childhood American Journal of Medical Genetics Part A ·Wen‐Hann Tan, Carlos A. Bacino, Steven A. Skinner, Irina Anselm, Rene Barbieri‐Welge, Astrid Bauer‐Carlin, Arthur L. Beaudet, Terry Jo Bichell, Jennifer Gentile, Daniel G. Glaze, Lucia T. Horowitz, Sanjeev V. Kothare, Hye‐Seung Lee, Mark Nespeca, Sarika U. Peters, Trilochan Sahoo, Dean Sarco, Susan E. Waisbren, Lynne M. Bird	2010	93
18	Insertional translocation detected using FISH confirmation of array‐comparative genomic hybridization (aCGH) results American Journal of Medical Genetics Part A ·Sung‐Hae Kang, Chad A. Shaw, Zhishuo Ou, Patricia A. Eng, M. Lance Cooper, Amber N. Pursley, Trilochan Sahoo, Carlos A. Bacino, A. Craig Chinault, Paweł Stankiewicz, Ankita Patel, James R. Lupski, Sau Wai Cheung	2010	81
19	Unique and atypical deletions in Prader–Willi syndrome reveal distinct phenotypes European Journal of Human Genetics ·Soo‐Jeong Kim, Jennifer Miller, Paul J. Kuipers, Jennifer R. German, Arthur L. Beaudet, Trilochan Sahoo, Daniel J. Driscoll	2011	79
20	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	76

About Trilochan Sahoo

Trilochan Sahoo is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Genetics, having authored 67 papers that have together received 4.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (29 papers), Prenatal Screening and Diagnostics (21 papers), Genetic Syndromes and Imprinting (16 papers), Chromosomal and Genetic Variations (9 papers), Genetics and Neurodevelopmental Disorders (8 papers), DNA Repair Mechanisms (7 papers), Epigenetics and DNA Methylation (7 papers) and Bacterial Genetics and Biotechnology (7 papers). The work is most often cited by research in Genetics (2.6k citations), Pediatrics, Perinatology and Child Health (971 citations), Molecular Biology (1.7k citations), Cognitive Neuroscience (407 citations) and Neurology (297 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, Daniela del Gaudio, Carlos A. Bacino, Jennifer R. German, Ankita Patel, Richard Person, Marwan Shinawi and Paweł Stankiewicz. 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

Trilochan Sahoo

Impact in

Papers in i

In The Last Decade

Trilochan Sahoo

Peers

Countries citing papers authored by Trilochan Sahoo

Fields of papers citing papers by Trilochan Sahoo

All Works

About Trilochan Sahoo

Explore authors with similar magnitude of impact

Papers in