Christopher M. Grochowski

2.5k total citations · 1 hit paper
34 papers, 751 citations indexed

About

Christopher M. Grochowski is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Christopher M. Grochowski has authored 34 papers receiving a total of 751 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 14 papers in Molecular Biology and 11 papers in Surgery. Recurrent topics in Christopher M. Grochowski's work include Genomic variations and chromosomal abnormalities (12 papers), Pediatric Hepatobiliary Diseases and Treatments (10 papers) and Chromosomal and Genetic Variations (8 papers). Christopher M. Grochowski is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Pediatric Hepatobiliary Diseases and Treatments (10 papers) and Chromosomal and Genetic Variations (8 papers). Christopher M. Grochowski collaborates with scholars based in United States, Sweden and Italy. Christopher M. Grochowski's co-authors include Nancy B. Spinner, Kathleen M. Loomes, Marcella Devoto, Claudia M.B. Carvalho, Ramakrishnan Rajagopalan, David A. Piccoli, Melissa A. Gilbert, Ellen Tsai, Ian D. Krantz and James R. Lupski and has published in prestigious journals such as Nucleic Acids Research, SHILAP Revista de lepidopterología and Nature Biotechnology.

In The Last Decade

Christopher M. Grochowski

31 papers receiving 744 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.

Detection of mosaic and population-level structural variants with Sniffles2

2024 118 citations Moritz Smolka, Luis F. Paulin et al. Nature Biotechnology profile →

Peers

Countries citing papers authored by Christopher M. Grochowski

Since Specialization

Citations

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

Fields of papers citing papers by Christopher M. Grochowski

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christopher M. Grochowski. 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 Christopher M. Grochowski. The network helps show where Christopher M. Grochowski may publish in the future.

Co-authorship network of co-authors of Christopher M. Grochowski

This figure shows the co-authorship network connecting the top 25 collaborators of Christopher M. Grochowski. A scholar is included among the top collaborators of Christopher M. Grochowski 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 Christopher M. Grochowski. Christopher M. Grochowski 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	Structural Variants: Mechanisms, Mapping, and Interpretation in Human Genetics 2025 ·Genes ·(unknown), Moez Dawood, Christopher M. Grochowski	0
2	An integrated platform for concurrent structural and single-nucleotide variants improves copy-number detection and reveals pathogenic alleles in undiagnosed Mendelian families 2025 ·Genome Medicine ·Haowei Du, (unknown), (unknown), (unknown), Christopher M. Grochowski, Michele G. Mehaffey, (unknown), (unknown), (unknown), (unknown), (unknown), Sebastian Ochoa, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown)	0
3	11: To remap or not to remap: the relevance of the genome references to resolve rare inversions 2025 ·Genetics in Medicine Open ·Claudia M.B. Carvalho, (unknown), (unknown), Jesper Eisfeldt, (unknown), (unknown), Medhat Mahmoud, Christopher M. Grochowski, Davut Pehli̇van, Fritz J. Sedlazeck, Jill A. Rosenfeld, Pengfei Liu, Weimin Bi, Ronit Marom, Anna Lindstrand	1
4	Detection of mosaic and population-level structural variants with Sniffles2 breakdown → 2024 ·Nature Biotechnology ·Moritz Smolka, Luis F. Paulin, Christopher M. Grochowski, Dominic W. Horner, Medhat Mahmoud, Sairam Behera, Ester Kalef-Ezra, Mira Gandhi, Karl Hong, Davut Pehli̇van, Sonja W. Scholz, Claudia M.B. Carvalho, Christos Proukakis, Fritz J. Sedlazeck	118
5	NODAL variants are associated with a continuum of laterality defects from simple D-transposition of the great arteries to heterotaxy 2024 ·Genome Medicine ·(unknown), Jawid M. Fatih, Angad Jolly, Moez Dawood, Haowei Du, Christopher M. Grochowski, Edward G. Jones, Shalini N. Jhangiani, Xander H.T. Wehrens, Pengfei Liu, Weimin Bi, Eric Boerwinkle, Jennifer E. Posey, Donna M. Muzny, Richard A. Gibbs, James R. Lupski, Zeynep Coban‐Akdemir, Shaine A. Morris	3
6	A combination of long- and short-read genomics reveals frequent p-arm breakpoints within chromosome 21 complex genomic rearrangements 2024 ·SHILAP Revista de lepidopterología ·(unknown), (unknown), Jasmin Lisfeld, (unknown), Christopher M. Grochowski, (unknown), Alex Hastie, (unknown), Sigrid Fuchs, Kornelia Neveling, Maja Hempel, Alexander Hoischen, Maria Pettersson, Claudia M.B. Carvalho, Jesper Eisfeldt, Anna Lindstrand	2
7	HMZDupFinder: a robust computational approach for detecting intragenic homozygous duplications from exome sequencing data 2023 ·Nucleic Acids Research ·Haowei Du, (unknown), Angad Jolly, Christopher M. Grochowski, Shalini N. Jhangiani, He Li, Donna M. Muzny, Jawid M. Fatih, Gözde Yeşil, Nursel Elçioğlu, Alper Gezdirici, Dana Marafi, Davut Pehli̇van, Daniel G. Calame, Claudia M.B. Carvalho, Jennifer E. Posey, Tomasz Gambin, Zeynep Coban‐Akdemir, James R. Lupski	2
8	De novo heterozygous variants in SLC30A7 are a candidate cause for Joubert syndrome 2022 ·American Journal of Medical Genetics Part A ·(unknown), Mohammad K. Eldomery, Lorraine Potocki, Dana Marafi, Jennifer E. Posey, Zeynep Coban‐Akdemir, Tamar Harel, Christopher M. Grochowski, Hailey Loucks, W. Patrick Devine, Jessica Van Ziffle, Dan Doherty, James R. Lupski, Joseph T.C. Shieh	3
9	Complex genomic rearrangements: an underestimated cause of rare diseases 2022 ·Trends in Genetics ·(unknown), Christopher M. Grochowski, Claudia M.B. Carvalho, Anna Lindstrand	29
10	Chromoanagenesis Event Underlies a de novo Pericentric and Multiple Paracentric Inversions in a Single Chromosome Causing Coffin–Siris Syndrome 2021 ·Frontiers in Genetics ·Christopher M. Grochowski, Ana Cristina Victorino Krepischi, Jesper Eisfeldt, Haowei Du, Débora Romeo Bertola, Danyllo Oliveira, Silvia Souza da Costa, James R. Lupski, Anna Lindstrand, Claudia M.B. Carvalho	7
11	Cytogenetically visible inversions are formed by multiple molecular mechanisms 2020 ·Human Mutation ·Maria Pettersson, Christopher M. Grochowski, Josephine Wincent, Jesper Eisfeldt, Amy M. Breman, Sau Wai Cheung, Ana Cristina Victorino Krepischi, Carla Rosenberg, James R. Lupski, (unknown), Lovisa Lovmar, (unknown), Elisabeth Syk Lundberg, Daniel Nilsson, Claudia M.B. Carvalho, Anna Lindstrand	11
12	Novel pathogenic genomic variants leading to autosomal dominant and recessive Robinow syndrome 2020 ·American Journal of Medical Genetics Part A ·Chaofan Zhang, Juliana F. Mazzeu, Jesper Eisfeldt, Christopher M. Grochowski, Janson J. White, Zeynep Coban‐Akdemir, Shalini N. Jhangiani, Donna M. Muzny, Richard A. Gibbs, Anna Lindstrand, James R. Lupski, V. Reid Sutton, Claudia M.B. Carvalho	14
13	Parental somatic mosaicism for CNV deletions – A need for more sensitive and precise detection methods in clinical diagnostics settings 2020 ·Genomics ·Qian Liu, Justyna A. Karolak, Christopher M. Grochowski, Theresa A. Wilson, Jill A. Rosenfeld, Carlos A. Bacino, Seema R. Lalani, Ankita Patel, Amy M. Breman, Janice Smith, Sau Wai Cheung, James R. Lupski, Weimin Bi, Paweł Stankiewicz	14
14	Distinct patterns of complex rearrangements and a mutational signature of microhomeology are frequently observed in PLP1 copy number gain structural variants 2019 ·Genome Medicine ·Vahid Bahrambeigi, Xiaofei Song, Karen Sperle, Christine R. Beck, Hadia Hijazi, Christopher M. Grochowski, Shen Gu, Pavel Seeman, Karen Woodward, Claudia M.B. Carvalho, Grace M. Hobson, James R. Lupski	20
15	Marker chromosome genomic structure and temporal origin implicate a chromoanasynthesis event in a family with pleiotropic psychiatric phenotypes 2018 ·Human Mutation ·Christopher M. Grochowski, Shen Gu, Bo Yuan, Julia TCW, Kristen Brennand, Jonathan Sebat, Dheeraj Malhotra, Shane McCarthy, Uwe Rudolph, Anna Lindstrand, Zechen Chong, Deborah L. Levy, James R. Lupski, Claudia M.B. Carvalho	19
16	CHRNA7 copy number gains are enriched in adolescents with major depressive and anxiety disorders 2018 ·Journal of Affective Disorders ·Madelyn A. Gillentine, (unknown), Jiani Yin, Christopher M. Grochowski, Janson J. White, Christian P. Schaaf, Chadi A. Calarge	12
17	A genome-wide association study identifies a susceptibility locus for biliary atresia on 2p16.1 within the gene EFEMP1 2018 ·PLoS Genetics ·(unknown), Melissa A. Gilbert, Christopher M. Grochowski, Deborah McEldrew, Jessica Llewellyn, Orith Waisbourd‐Zinman, Håkon Håkonarson, Joan E. Bailey‐Wilson, Pierre Russo, Rebecca G. Wells, Kathleen M. Loomes, Nancy B. Spinner, Marcella Devoto	47
18	CHRNA7 Deletions are Enriched in Risperidone-Treated Children and Adolescents 2017 ·Journal of Child and Adolescent Psychopharmacology ·Madelyn A. Gillentine, Janson J. White, Christopher M. Grochowski, James R. Lupski, Christian P. Schaaf, Chadi A. Calarge	8
19	THBS2 Is a Candidate Modifier of Liver Disease Severity in Alagille Syndrome 2016 ·Cellular and Molecular Gastroenterology and Hepatology ·Ellen Tsai, Melissa A. Gilbert, Christopher M. Grochowski, Lara A. Underkoffler, He Meng, Xiaojie Zhang, Michael M. Wang, (unknown), Kurt D. Hankenson, David A. Piccoli, Henry C. Lin, Binita M. Kamath, Marcella Devoto, Nancy B. Spinner, Kathleen M. Loomes	31
20	Jagged1 (JAG1): Structure, expression, and disease associations 2015 ·Gene ·Christopher M. Grochowski, Kathleen M. Loomes, Nancy B. Spinner	95

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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