Sat Dev Batish

6.8k total citations · 1 hit paper
50 papers, 3.6k citations indexed

About

Sat Dev Batish is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Sat Dev Batish has authored 50 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Molecular Biology, 17 papers in Genetics and 14 papers in Cellular and Molecular Neuroscience. Recurrent topics in Sat Dev Batish's work include DNA Repair Mechanisms (21 papers), Genetic Neurodegenerative Diseases (10 papers) and BRCA gene mutations in cancer (8 papers). Sat Dev Batish is often cited by papers focused on DNA Repair Mechanisms (21 papers), Genetic Neurodegenerative Diseases (10 papers) and BRCA gene mutations in cancer (8 papers). Sat Dev Batish collaborates with scholars based in United States, Germany and China. Sat Dev Batish's co-authors include Arleen D. Auerbach, Helmut Hanenberg, Philip F. Giampietro, Jaya M. Satagopan, David I. Kutler, Bhuvanesh Singh, Orna Levran, James R. Lupski, Charles F. Towne and Feng Zhang and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Blood.

In The Last Decade

Sat Dev Batish

48 papers receiving 3.5k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A 20-year perspective on the International Fanconi Anemia Registry (IFAR)

2003 527 citations Sat Dev Batish, Philip F. Giampietro et al. profile →

Peers

Countries citing papers authored by Sat Dev Batish

Since Specialization

Citations

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

Fields of papers citing papers by Sat Dev Batish

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sat Dev Batish. 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 Sat Dev Batish. The network helps show where Sat Dev Batish may publish in the future.

Co-authorship network of co-authors of Sat Dev Batish

This figure shows the co-authorship network connecting the top 25 collaborators of Sat Dev Batish. A scholar is included among the top collaborators of Sat Dev Batish 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 Sat Dev Batish. Sat Dev Batish 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	Expanding the Phenotype of Extremely Early Onset Juvenile Huntington's Disease: A Case Report and Review of Previously Published Cases 2024 ·American Journal of Medical Genetics Part A ·Zöe Powis, (unknown), (unknown), (unknown), Sat Dev Batish	1
2	HTT CAG Repeat Length Variation in Huntington Disease (HD) Patients: Experience from a US Reference Laboratory (2376) 2021 ·Neurology ·Sat Dev Batish, (unknown), (unknown), (unknown), Zhenyuan Wang, Vivekananda Datta, Thomas D. Mullen, Jeff Radcliff	1
3	Limbic encephalitis in a child with ovarian teratoma and influenza B. Case report and critical review of the history of autoimmune anti-N-methyl-d-aspartate receptor encephalitis 2021 ·Journal of Neuroimmunology ·(unknown), (unknown), (unknown), Sat Dev Batish, William D. Brown	1
4	Analysis of Association of Deletion in the Repeat Region of the Periaxin Gene With Late Onset Motor Neuropathy 2013 ·Journal of Neurology Research ·Leema Reddy Peddareddygari, (unknown), (unknown), Masamichi Ito, Sat Dev Batish, Raji P. Grewal	0
5	Functional assessment of TSC1 missense variants identified in individuals with tuberous sclerosis complex 2011 ·Human Mutation ·Marianne Hoogeveen‐Westerveld, Rosemary Ekong, Sue Povey, Izabela Karbassi, Sat Dev Batish, Johan T. den Dunnen, Agnies M. van Eeghen, Elizabeth A. Thiele, Karin Mayer, Kira A. Dies, Wen Li, Catherine Thompson, Steven Sparagana, Peter Maxwell Davies, Cora M. Aalfs, Ans van den Ouweland, Dicky Halley, Mark Nellist	34
6	Alu-specific microhomology-mediated deletion of the final exon of SPAST in three unrelated subjects with hereditary spastic paraplegia 2011 ·Genetics in Medicine ·Philip M. Boone, Pengfei Liu, Feng Zhang, Cláudia Carvalho, Charles F. Towne, Sat Dev Batish, James R. Lupski	37
7	Denys-Drash Syndrome with Neonatal Renal Failure in Monozygotic Twins Due to C.1097G>A Mutation in the WT1 Gene 2011 ·Fetal and Pediatric Pathology ·Larissa V. Furtado, Theodore J. Pysher, John M. Opitz, (unknown), Jessica Comstock, Sat Dev Batish, Teri Jo Mauch, Raoul D. Nelson, Holly Zhou	4
8	Severe Dilated Cardiomyopathy in a Patient With Myotonic Dystrophy Type 2 and Homozygous Repeat Expansion in ZNF9 2011 ·Congestive Heart Failure ·Teresa M. Lee, Mathew S. Maurer, Izabela Karbassi, Corey Braastad, Sat Dev Batish, Wendy K. Chung	11
9	GJB1/Connexin 32 whole gene deletions in patients with X-linked Charcot–Marie–Tooth disease 2010 ·Neurogenetics ·Claudia Gonzaga‐Jauregui, Feng Zhang, Charles F. Towne, Sat Dev Batish, James R. Lupski	23
10	Dystrophinopathy in Girls With Limb Girdle Muscular Dystrophy Phenotype 2010 ·Journal of Clinical Neuromuscular Disease ·Sailaja Golla, Satish Agadi, Dennis K. Burns, Warren A. Marks, Sat Dev Batish, Daniela del Gaudio, Susan T. Iannaccone	5
11	Novel MPZ mutations and congenital hypomyelinating neuropathy 2010 ·Neuromuscular Disorders ·Hugh J. McMillan, Sandro Santagata, Frederic Shapiro, Sat Dev Batish, (unknown), (unknown), Peter B. Kang	11
12	Polycystic Ovaries and Adrenal Insufficiency in a Young Pubescent Female with Lipoid Congenital Adrenal Hyperplasia Due to Splice Mutation of the StAR Gene: A Case Report and Review of the Literature 2010 ·Journal of Pediatric Endocrinology and Metabolism ·(unknown), (unknown), Sat Dev Batish, Patrick G. Brosnan	9
13	Mechanisms for Nonrecurrent Genomic Rearrangements Associated with CMT1A or HNPP: Rare CNVs as a Cause for Missing Heritability 2010 ·The American Journal of Human Genetics ·Feng Zhang, Pavel Seeman, Pengfei Liu, Marian A. J. Weterman, Claudia Gonzaga‐Jauregui, Charles F. Towne, Sat Dev Batish, Els De Vriendt, Peter De Jonghe, Bernd Rautenstrauß, (unknown), Mehrdad Khajavi, (unknown), Antoon Vandenberghe, Francesc Palau, Lionel Van Maldergem, Frank Baas, Vincent Timmerman, James R. Lupski	98
14	The DNA replication FoSTeS/MMBIR mechanism can generate genomic, genic and exonic complex rearrangements in humans 2009 ·Nature Genetics ·Feng Zhang, Mehrdad Khajavi, Anne M. Connolly, Charles F. Towne, Sat Dev Batish, James R. Lupski	333
15	Identification and characterization of mutations in FANCL gene: A second case of Fanconi anemia belonging to FA-L complementation group 2009 ·Human Mutation ·Abdullah Mahmood Ali, Michelle Kirby, Michael Jansen, Francis P. Lach, Jennifer Schulte, Thiyam Ramsing Singh, Sat Dev Batish, Arleen D. Auerbach, David A. Williams, Amom Ruhikanta Meetei	18
16	Biallelic mutations in PALB2 cause Fanconi anemia and predispose to childhood cancer 2007 ·Cancer Research ·Sarah Reid, Detlev Schindler, Helmut Hanenberg, Marc Tischkowitz, Sandra Hanks, Karen Barker, Patrick Kelly, Sheila Seal, Sat Dev Batish, Francis P. Lach, Reinhard Kalb, Kornelia Neveling, Christopher G. Mathew, Arleen D. Auerbach, Nazneen Rahman	1
17	Anti-MuSK Myasthenia Gravis Presenting With Purely Ocular Findings 2005 ·Archives of Neurology ·James B. Caress, Christopher H. Hunt, Sat Dev Batish	42
18	Shared Genetic Susceptibility to Breast Cancer, Brain Tumors, and Fanconi Anemia 2003 ·JNCI Journal of the National Cancer Institute ·Kenneth Offit, Orna Levran, Brendan Mullaney, Kandice Mah, Khédoudja Nafa, Sat Dev Batish, Roberta A. Diotti, (unknown), Amie M. Deffenbaugh, Thomas Scholl, V. Proud, Mark E. Robson, Larry Norton, Nathan A. Ellis, Helmut Hanenberg, Arleen D. Auerbach	122
19	Spectrum of sequence variation in theFANCG gene: An International Fanconi Anemia Registry (IFAR) study 2003 ·Human Mutation ·Arleen D. Auerbach, Jason Greenbaum, Kanan Pujara, Sat Dev Batish, Marco A. Bitencourt, (unknown), (unknown), (unknown), Ricardo Pasqüini, Philip F. Giampietro, Helmut Hanenberg, Orna Levran	29
20	Phenotypic correction of primary Fanconi anemia T cells with retroviral vectors as a diagnostic tool 2002 ·Experimental Hematology ·Helmut Hanenberg, Sat Dev Batish, Karen E. Pollok, (unknown), Peter C. Verlander, Cordula Leurs, Ryan Cooper, (unknown), Laura S. Haneline, D. Wade Clapp, Stephan Lobitz, David A. Williams, Arleen D. Auerbach	71

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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