Malini Sathanoori

727 total citations
21 papers, 462 citations indexed

About

Malini Sathanoori is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Malini Sathanoori has authored 21 papers receiving a total of 462 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 8 papers in Molecular Biology and 5 papers in Pathology and Forensic Medicine. Recurrent topics in Malini Sathanoori's work include Genomic variations and chromosomal abnormalities (11 papers), Cancer Genomics and Diagnostics (5 papers) and Congenital heart defects research (4 papers). Malini Sathanoori is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Cancer Genomics and Diagnostics (5 papers) and Congenital heart defects research (4 papers). Malini Sathanoori collaborates with scholars based in United States, Australia and India. Malini Sathanoori's co-authors include Steven H. Swerdlow, Raju Pillai, S. Branden Van Oss, Urvashi Surti, Jie Hu, Shubha Tole, Vidita A. Vaidya, Andreas H. Kottmann, Jun Liao and Richa Kapoor and has published in prestigious journals such as Endocrinology, The American Journal of Surgical Pathology and American Journal of Clinical Pathology.

In The Last Decade

Malini Sathanoori

21 papers receiving 443 citations

Peers

Countries citing papers authored by Malini Sathanoori

Since Specialization

Citations

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

Fields of papers citing papers by Malini Sathanoori

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Malini Sathanoori

This figure shows the co-authorship network connecting the top 25 collaborators of Malini Sathanoori. A scholar is included among the top collaborators of Malini Sathanoori based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Malini Sathanoori. Malini Sathanoori is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Optical genome mapping in acute myeloid leukemia: a multicenter evaluation 2022 ·Blood Advances ·Brynn Levy, Linda B. Baughn, Yassmine Akkari, Scott Chartrand, (unknown), David F. Claxton, Patrick A. Lennon, (unknown), Ravindra Kolhe, (unknown), Beth A. Pitel, Nikhil Sahajpal, Malini Sathanoori, George Vlad, Lijun Zhang, Min Fang, Rashmi Kanagal‐Shamanna, James R. Broach	65
2	Deletion of conserved non‐coding sequences downstream from NKX2‐1: A novel disease‐causing mechanism for benign hereditary chorea 2021 ·Molecular Genetics & Genomic Medicine ·Jun Liao, Keith A. Coffman, Joseph Locker, Quasar Saleem Padiath, Bruce Nmezi, Robyn A. Filipink, Jie Hu, Malini Sathanoori, Suneeta Madan‐Khetarpal, Marianne McGuire, Allison Schreiber, Rocio Moran, Neil Friedman, Lori Hoffner, Aleksandar Rajkovic, Svetlana A. Yatsenko, Urvashi Surti	4
3	20. A resource for our clinical genomics community: The Compendium of Cancer Genome Aberrations (CCGA) 2020 ·Cancer Genetics ·Jennelle C. Hodge, Beth A. Pitel, Brian Davis, Linda D. Cooley, Hui Chen, Scott Newman, Ying Zou, Kilannin Krysiak, Soheil Shams, Fei Yang, Malini Sathanoori, Fabiola Quintero‐Rivera, (unknown), Daynna J. Wolff	1
4	5. Progress and future of the compendium of Cancer Genome Aberrations (CCGA) 2018 ·Cancer Genetics ·Jennelle C. Hodge, Linda D. Cooley, (unknown), Fei Yang, Beth A. Pitel, Malini Sathanoori, Brian Davis, (unknown), Obi L. Griffith, Linda B. Baughn, Scott Newman, Daynna J. Wolff	1
5	Chromosomal microarray provides enhanced targetable gene aberration detection when paired with next generation sequencing panel in profiling lung and colorectal tumors 2016 ·Cancer Genetics ·Sandeep Mukherjee, (unknown), Scott R. Wheeler, Malini Sathanoori, Christopher D. Coldren, James L. Prescott, Natalia Kozyr, Mark Bouzyk, Mick Correll, Hao Ho, Pranil Chandra, Patrick A. Lennon	6
6	CNTN6 copy number variations in 14 patients: a possible candidate gene for neurodevelopmental and neuropsychiatric disorders 2015 ·Journal of Neurodevelopmental Disorders ·Jie Hu, Jun Liao, Malini Sathanoori, (unknown), Jessica Sebastian, Svetlana A. Yatsenko, Urvashi Surti	52
7	A novel maternally inherited 8q24.3 and a rare paternally inherited 14q23.3 CNVs in a family with neurodevelopmental disorders 2015 ·American Journal of Medical Genetics Part A ·Jie Hu, Malini Sathanoori, (unknown), Meron Azage, (unknown), Suneeta Madan‐Khetarpal, Amy Goldstein, Urvashi Surti	16
8	Whole-Genome Single Nucleotide Polymorphism Array Analysis Is Complementary to Classical Cytogenetic Analysis in the Evaluation of Lymphoid Proliferations 2014 ·American Journal of Clinical Pathology ·Sarah E. Gibson, Jianhua Luo, Malini Sathanoori, Jun Liao, Urvashi Surti, Steven H. Swerdlow	6
9	Double-hit B-cell Lymphomas With BCL6 and MYC Translocations Are Aggressive, Frequently Extranodal Lymphomas Distinct From BCL2 Double-hit B-cell Lymphomas 2013 ·The American Journal of Surgical Pathology ·Raju Pillai, Malini Sathanoori, S. Branden Van Oss, Steven H. Swerdlow	130
10	Thyroid carcinoma-associated genetic mutations also occur in thyroid lymphomas 2012 ·Modern Pathology ·Nidhi Aggarwal, Steven H. Swerdlow, Lindsey Kelly, Jennifer B. Ogilvie, (unknown), Malini Sathanoori, Yuri E. Nikiforov	17
11	Co‐existence of 9p deletion and Silver‐Russell syndromes in a patient with maternally inherited cryptic complex chromosome rearrangement involving chromosomes 4, 9, and 11 2012 ·American Journal of Medical Genetics Part A ·Jie Hu, Malini Sathanoori, (unknown), Suneeta Madan‐Khetarpal, Marianne McGuire, Urvashi Surti	12
12	Prenatal Diagnosis of 2q32 Deletion Syndrome Characterized by Multiple Segmental Deletions and Complex Chromosomal Rearrangement Involving Chromosomes 2, 5 and 7 2012 ·Fetal Diagnosis and Therapy ·(unknown), Urvashi Surti, Malini Sathanoori, (unknown), Beth A. Torchia, Aleksandar Rajkovic	1
13	Prenatal detection of del(10)(q11.2) mosaicism in chorionic villus specimens likely caused by a common chromosomal fragile site FRA10G is associated with a normal phenotype 2012 ·Prenatal Diagnosis ·Jun Liao, Malini Sathanoori, Svetlana A. Yatsenko, Jie Hu, (unknown), Lori Hoffner, W. Allen Hogge, Urvashi Surti	1
14	Three Supernumerary Marker Chromosomes in a Patient with Developmental Delay, Mental Retardation, and Dysmorphic Features 2011 ·PubMed ·Jie Hu, Suneeta Madan‐Khetarpal, (unknown), (unknown), Stephanie J. DeWard, Malini Sathanoori, Urvashi Surti	3
15	Molecular and clinical characterization of a recurrent cryptic unbalanced t(4q;18q) resulting in an 18q deletion and 4q duplication 2008 ·American Journal of Medical Genetics Part A ·Craig Horbinski, (unknown), Patricia Heard, Malini Sathanoori, Jie Hu, Jerry Vockley, Shelly Gunn, Daniel E. Hale, Urvashi Surti, Jannine D. Cody	18
16	Cytogenetic Abnormalities Detected by Fluorescence In Situ Hybridization on Paraffin-Embedded Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma Lymphoid Tissue Biopsy Specimens 2008 ·American Journal of Clinical Pathology ·Melina Flanagan, Malini Sathanoori, Urvashi Surti, Lorinda Soma, Steven H. Swerdlow	15
17	Cryptic duplication of 12q24.33 → qter in a child with Angelman syndrome—simultaneous occurrence of two unrelated cytogenetic events 2007 ·American Journal of Medical Genetics Part A ·Malini Sathanoori, Jie Hu, (unknown), (unknown), Jerry Vockley, (unknown), Jirair K. Bedoyan, S. M. Jalal, (unknown), Urvashi Surti	5
18	Derivative (14)t(11;14)(q13;q32)t(11;14)(p11.2;p11.2): a novel unbalanced variant of the t(11;14)(q13;q32) translocation in mantle cell lymphoma 2007 ·Cancer Genetics and Cytogenetics ·Malini Sathanoori, (unknown), Stanley M. Marks, Steven H. Swerdlow	2
19	Application of Multicolor Banding for Identification of Complex Chromosome 18 Rearrangements 2006 ·Journal of Molecular Diagnostics ·Jie Hu, Malini Sathanoori, (unknown), Urvashi Surti	6
20	Differential regulation of multiple brain-derived neurotrophic factor transcripts in the postnatal and adult rat hippocampus during development, and in response to kainate administration 2004 ·Molecular Brain Research ·Malini Sathanoori, Brian Dias, Amrita R. Nair, Sunayana B. Banerjee, Shubha Tole, Vidita A. Vaidya	31

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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