Blake C. Ballif

11.7k total citations
75 papers, 4.0k citations indexed

About

Blake C. Ballif is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Blake C. Ballif has authored 75 papers receiving a total of 4.0k indexed citations (citations by other indexed papers that have themselves been cited), including 61 papers in Genetics, 38 papers in Molecular Biology and 26 papers in Plant Science. Recurrent topics in Blake C. Ballif's work include Genomic variations and chromosomal abnormalities (51 papers), Chromosomal and Genetic Variations (26 papers) and Prenatal Screening and Diagnostics (18 papers). Blake C. Ballif is often cited by papers focused on Genomic variations and chromosomal abnormalities (51 papers), Chromosomal and Genetic Variations (26 papers) and Prenatal Screening and Diagnostics (18 papers). Blake C. Ballif collaborates with scholars based in United States, Canada and Spain. Blake C. Ballif's co-authors include Lisa G. Shaffer, Bassem A. Bejjani, Jill A. Rosenfeld, Justine Coppinger, Catherine D. Kashork, Beth S. Torchia, Aaron Theisen, Kyle Sundin, Emily A. Rorem and J. Britt Ravnan and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and PLoS ONE.

In The Last Decade

Blake C. Ballif

75 papers receiving 3.8k citations

Peers

Countries citing papers authored by Blake C. Ballif

Since Specialization

Citations

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

Fields of papers citing papers by Blake C. Ballif

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Blake C. Ballif. 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 Blake C. Ballif. The network helps show where Blake C. Ballif may publish in the future.

Co-authorship network of co-authors of Blake C. Ballif

This figure shows the co-authorship network connecting the top 25 collaborators of Blake C. Ballif. A scholar is included among the top collaborators of Blake C. Ballif 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 Blake C. Ballif. Blake C. Ballif 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	Identification of aneuploidy in dogs screened by a SNP microarray 2021 ·Human Genetics ·Lisa G. Shaffer, (unknown), M. Świtoński, (unknown), Blake C. Ballif	3
2	The PMEL gene and merle (dapple) in the dachshund: cryptic, hidden, and mosaic variants demonstrate the need for genetic testing prior to breeding 2021 ·Human Genetics ·Blake C. Ballif, (unknown), (unknown), (unknown), Kyle Sundin, (unknown), Lisa G. Shaffer	1
3	Standards and guidelines for canine clinical genetic testing laboratories 2018 ·Human Genetics ·Lisa G. Shaffer, Kyle Sundin, (unknown), (unknown), June Swinburne, (unknown), (unknown), (unknown), Blake C. Ballif	9
4	Large Inverted Duplications in the Human Genome Form via a Fold-Back Mechanism 2014 ·PLoS Genetics ·Karen Hermetz, Scott Newman, Karen N. Conneely, Alastair J. Martin, Blake C. Ballif, Lisa G. Shaffer, Jannine D. Cody, M. Katharine Rudd	54
5	Modified Array-based Comparative Genomic Hybridization Detects Cryptic and Variant PML-RARA Rearrangements in Acute Promyelocytic Leukemia Lacking Classic Translocations 2013 ·Diagnostic Molecular Pathology ·Aaron M. Gruver, Heesun J. Rogers, James R. Cook, Blake C. Ballif, Roger A. Schultz, Jacqueline R. Batanian, (unknown), Raymond R. Tubbs	6
6	Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypes 2012 ·European Journal of Human Genetics ·(unknown), Jill A. Rosenfeld, Ryan N. Traylor, G. Bradley Schaefer, Elizabeth McPherson, Blake C. Ballif, Eva Klopocki, Stefan Mundlos, Lisa G. Shaffer, Arthur S. Aylsworth	82
7	Recurrence, submicroscopic complexity, and potential clinical relevance of copy gains detected by array CGH that are shown to be unbalanced insertions by FISH 2011 ·Genome Research ·Nicholas J. Neill, Blake C. Ballif, Allen N. Lamb, Sumit Parikh, J. Britt Ravnan, Roger A. Schultz, Beth S. Torchia, Jill A. Rosenfeld, Lisa G. Shaffer	41
8	Evaluation of chronic lymphocytic leukemia by oligonucleotide-based microarray analysis uncovers novel aberrations not detected by FISH or cytogenetic analysis 2011 ·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, (unknown), (unknown), (unknown), Nicholas J. Neill, (unknown), (unknown), Trilochan Sahoo, Blake C. Ballif, Lisa G. Shaffer	10
9	Response to the letter by Collins and Schimke 2011 ·Genetics in Medicine ·(unknown), Justine Coppinger, Blake C. Ballif, Lisa G. Shaffer, Jay W. Ellison, Sulagna C. Saitta, Tracy Stroud, Kandamurugu Manickam, Zheng Fan	2
10	Diverse mutational mechanisms cause pathogenic subtelomeric rearrangements 2011 ·Human Molecular Genetics ·Yue Luo, Karen Hermetz, (unknown), Jennifer G. Mullé, Anne Dodd, Karen D. Tsuchiya, Blake C. Ballif, Lisa G. Shaffer, Jannine D. Cody, David H. Ledbetter, Alastair J. Martin, M. Katharine Rudd	31
11	Comparative analysis of copy number detection by whole-genome BAC and oligonucleotide array CGH 2010 ·Molecular Cytogenetics ·Nicholas J. Neill, Beth S. Torchia, Bassem A. Bejjani, Lisa G. Shaffer, Blake C. Ballif	48
12	Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity 2010 ·Genetics in Medicine ·Ruxandra Bachmann‐Gagescu, Heather C. Mefford, Charles A. Cowan, Gwen M. Glew, Anne Hing, Stephanie E Wallace, Patricia I. Bader, (unknown), Pamela J. Reitnauer, Rosemarie Smith, David W. Stockton, Hiltrud Muhle, Ingo Helbig, Evan E. Eichler, Blake C. Ballif, Jill A. Rosenfeld, Karen D. Tsuchiya	137
13	Small Deletions of SATB2 Cause Some of the Clinical Features of the 2q33.1 Microdeletion Syndrome 2009 ·PLoS ONE ·Jill A. Rosenfeld, Blake C. Ballif, Ann Lucas, (unknown), Cynthia M. Powell, Arthur S. Aylsworth, Beth A. Torchia, Lisa G. Shaffer	93
14	Genotype–phenotype analysis of TCF4 mutations causing Pitt-Hopkins syndrome shows increased seizure activity with missense mutations 2009 ·Genetics in Medicine ·Jill A. Rosenfeld, Kathleen A. Leppig, Blake C. Ballif, Heidi Thiese, Christine Erdie-Lalena, (unknown), (unknown), J. Edward Spence, Anne M. Bandholz, Urvashi Surti, Jonathan Zonana, Kory Keller, Wendy S. Meschino, Bassem A. Bejjani, Beth S. Torchia, Lisa G. Shaffer	55
15	Development of a high-density pericentromeric region BAC clone set for the detection and characterization of small supernumerary marker chromosomes by array CGH 2007 ·Genetics in Medicine ·Blake C. Ballif, (unknown), (unknown), (unknown), (unknown), Emily A. Rorem, Aaron Theisen, Bassem A. Bejjani, Lisa G. Shaffer	46
16	The clinical utility of enhanced subtelomeric coverage in array CGH 2007 ·American Journal of Medical Genetics Part A ·Blake C. Ballif, (unknown), (unknown), (unknown), Aaron Theisen, Bassem A. Bejjani, Lisa G. Shaffer	60
17	Targeted genomic microarray analysis for identification of chromosome abnormalities in 1500 consecutive clinical cases 2006 ·The Journal of Pediatrics ·Lisa G. Shaffer, Catherine D. Kashork, Reza Saleki, Emily A. Rorem, Kyle Sundin, Blake C. Ballif, Bassem A. Bejjani	165
18	Use of targeted array‐based CGH for the clinical diagnosis of chromosomal imbalance: Is less more? 2005 ·American Journal of Medical Genetics Part A ·Bassem A. Bejjani, Reza Saleki, Blake C. Ballif, Emily A. Rorem, Kyle Sundin, Aaron Theisen, Catherine D. Kashork, Lisa G. Shaffer	155
19	Delineation of mechanisms and regions of dosage imbalance in complex rearrangements of 1p36 leads to a putative gene for regulation of cranial suture closure 2004 ·European Journal of Human Genetics ·Marzena Gajęcka, Wei Yu, Blake C. Ballif, Caron D. Glotzbach, (unknown), Chad A. Shaw, Catherine D. Kashork, Heidi A. Heilstedt, (unknown), Aaron Theisen, Ritva Rice, David Rice, Lisa G. Shaffer	68
20	Physical Map of 1p36, Placement of Breakpoints in Monosomy 1p36, and Clinical Characterization of the Syndrome 2003 ·The American Journal of Human Genetics ·Heidi A. Heilstedt, Blake C. Ballif, (unknown), Richard A. Lewis, Samuel Stal, Catherine D. Kashork, Carlos A. Bacino, Stuart K. Shapira, Lisa G. Shaffer	181

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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