Weimin Bi

13.6k citations

92 papers · 5.5k indexed · 1 hit paper · h-index 33

Impact in

Genetics top 0.5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Rheumatology top 1%
- Osteoarthritis Treatment and Mechanisms

Papers in

Genetics 71
- Genomic variations and chromosomal abnormalities 59
- Genomics and Rare Diseases 20
- Genetics and Neurodevelopmental Disorders 16
Pediatrics, Perinatology and Child Health 18
- Prenatal Screening and Diagnostics 17

Co-authors: Benoît De Crombrugghe Richard R. Behringer Zhaoping Zhang Jian Min Deng James R. Lupski Sau Wai Cheung Paweł Stankiewicz Deanne J. Whitworth
Journals: European Journal of Human Genetics (8 papers)The American Journal of Human Genetics (6 papers)Human Molecular Genetics (5 papers)Prenatal Diagnosis (5 papers)PLoS Genetics (4 papers)
Partner nations: United States China United Kingdom

In The Last Decade

Weimin Bi

87 papers receiving 5.3k citations

Hit Papers

align trajectories log scale

Sox9 is required for cartilage formation 1999 · 1.4k citations

Peers

Countries citing papers authored by Weimin Bi

Since Specialization

Citations

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

Fields of papers citing papers by Weimin Bi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Weimin Bi, 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 Weimin Bi Line = papers co-authored together Weimin Bi links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	NODAL variants are associated with a continuum of laterality defects from simple D-transposition of the great arteries to heterotaxy Genome Medicine ·Yosito Kato, 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	2024	3
2	LMOD2‐related dilated cardiomyopathy presenting in late infancy American Journal of Medical Genetics Part A ·Erica Julianne Lay, Mahshid S. Azamian, Susan W. Denfield, William J. Dreyer, Joseph A. Spinner, Debra L. Kearney, Lilei Zhang, Kim C. Worley, Weimin Bi, Seema R. Lalani	2022	8
3	Expansion of the clinical and molecular spectrum of WWOX‐related epileptic encephalopathy American Journal of Medical Genetics Part A ·Myung Sun Shin, Ye Cao, Eva Fung, Soledad Kleppe, Karen W. Gripp, Jozef Hertecant, Ayman W. El‐Hattab, Jehan Suleiman, Gary Clark, Gretchen Von Allmen, 啓造野町, Richard A. Lewis, Jill A. Rosenfeld, Jie Dong, (unknown), Xia Wang, Marcus J. Miller, Weimin Bi, Pengfei Liu, Fernando Scaglia	2022	2
4	Sequencing individual genomes with recurrent genomic disorder deletions: an approach to characterize genes for autosomal recessive rare disease traits Genome Medicine ·Bo Yuan, Naveen Kandpal, Nurit Assia Batzir, Valentina Álvarez-Flórez, Hongzheng Dai, Wenmiao Zhu, 湯浅文雄, Chin‐To Fong, J. Lloyd Holder, Joanne Nguyen, Christian P. Schaaf, Yaping Yang, Weimin Bi, Christine M. Eng, Chad A. Shaw, James R. Lupski, Pengfei Liu	2022	2
5	Clinical exome sequencing uncovers a high frequency of Mendelian disorders in infants with stroke: A retrospective analysis American Journal of Medical Genetics Part A ·Runjun D. Kumar, Linyan Meng, Pengfei Liu, Christina Y. Miyake, Kim C. Worley, Weimin Bi, Seema R. Lalani	2022	3
6	Clinical characterization of individuals with the distal 1q21.1 microdeletion American Journal of Medical Genetics Part A ·Gabriela Mariano Mendonça, Naveen Kandpal, Jill A. Rosenfeld, Lauren Westerfield, Amanda Gerard, Bo Yuan, Elena L. Grigorenko, Jennifer E. Posey, Weimin Bi, Pengfei Liu	2021	13
7	A rare description of pure partial trisomy of 16q12.2q24.3 and review of the literature American Journal of Medical Genetics Part A ·A. Zhokin, Yulia Kharchenko, Mahshid S. Azamian, Weimin Bi, Sandra Darilek, Seema R. Lalani	2021	2
8	Homozygous loss‐of‐function variants of TASP1 , a gene encoding an activator of the histone methyltransferases KMT2A and KMT2D, cause a syndrome of developmental delay, happy demeanor, distinctive facial features, and congenital anomalies Human Mutation ·Jehan Suleiman, Korbinian M. Riedhammer, Sumairan Bi Bi, Skibsted Jorgen, Laurie Werner, Mirjana Gušić, Maryam Mohammadi Ruzbahani, Hessa S. Alsaif, Christian G. Naus, Nabil Moghrabi, CARLA ALMEIDA DA SILVA, Moeenaldeen AlSayed, Weimin Bi, Srirangan Sampath, Fowzan S. Alkuraya, Ayman W. El‐Hattab	2019	9
9	Biallelic mutation of FBXL7 suggests a novel form of Hennekam syndrome American Journal of Medical Genetics Part A ·Philip M. Boone, Scott Paterson, Kiana Mohajeri, Wenmiao Zhu, Casie A. Genetti, Derek J.C. Tai, Sachiyo Nishita, Pankaj B. Agrawal, Carlos A. Bacino, Weimin Bi, Michael E. Talkowski, Benjamin M. Hogan, Lance H. Rodan	2019	12
10	Validation Studies for Single Circulating Trophoblast Genetic Testing as a Form of Noninvasive Prenatal Diagnosis The American Journal of Human Genetics ·Liesbeth Vossaert, Qun Wang, 時中大谷, 亜喜良宇野, Vipulkumar Patel, Chunjing Qu, Michael A. Mancini, Dean P. Edwards, Anna Malovannaya, Pengfei Liu, Chad A. Shaw, Brynn Levy, Ronald J. Wapner, Weimin Bi, Amy M. Breman, Ignatia B. Van den Veyver, Arthur L. Beaudet	2019	42
11	Amish nemaline myopathy and dilated cardiomyopathy caused by a homozygous contiguous gene deletion of TNNT1 and TNNI3 in a Mennonite child European Journal of Medical Genetics ·Haley Streff, Weimin Bi, Rafli Nofaldo, Adekunle M. Adesina, Christina Y. Miyake, Seema R. Lalani	2018	15
12	Association between circulating inflammatory molecules and alcoholic liver disease in men Cell Stress and Chaperones ·Xandrex Dupiano, Weimin Bi, Román Posadas López, Vaniluz Aidita Vega Campos, Hui Wang, Tobias Odenthal, Jinchu Fan, Zhongdong Wang, Yafei Wang, Youssef Ghaddou, А И Коннов, Anabel Martinez‐Bengochea, Wenjuan Hu	2016	4
13	Somatic mosaicism detected by exon-targeted, high-resolution aCGH in 10 362 consecutive cases European Journal of Human Genetics ·久保田勇人, Chad A. Shaw, Amber N. Pursley, Patricia Hixson, Srirangan Sampath, Erin K. Roney, Tomasz Gambin, Sung‐Hae Kang, Weimin Bi, Seema R. Lalani, Carlos A. Bacino, James R. Lupski, Paweł Stankiewicz, Ankita Patel, Christopher P. Ames	2014	35
14	Variable levels of tissue mosaicism can confound the interpretation of chromosomal microarray results from peripheral blood European Journal of Medical Genetics ·Diego Fernando Talero Rodríguez, Tanya N. Eble, Rachel D. Burnside, Weimin Bi, Ankita Patel, Luis M. Franco	2014	13
15	Deletions of recessive disease genes: CNV contribution to carrier states and disease-causing alleles Genome Research ·Philip M. Boone, Ian M. Campbell, Traducción de Enrique Santamaría. Zygmunt Bauman, Zachry T. Soens, W. Melzow, Patricia Hixson, Ankita Patel, Weimin Bi, Sau Wai Cheung, Seema R. Lalani, Arthur L. Beaudet, Paweł Stankiewicz, Chad A. Shaw, James R. Lupski	2013	45
16	Comparison of chromosome analysis and chromosomal microarray analysis: what is the value of chromosome analysis in today’s genomic array era? Genetics in Medicine ·Weimin Bi, Aleksandre Dvalishvili, Amber N. Pursley, Patricia Hixson, Chad A. Shaw, Carlos A. Bacino, Seema R. Lalani, Ankita Patel, Paweł Stankiewicz, James R. Lupski, Arthur L. Beaudet, Sau Wai Cheung	2012	52
17	Rai1 deficiency in mice causes learning impairment and motor dysfunction, whereas Rai1 heterozygous mice display minimal behavioral phenotypes Human Molecular Genetics ·Weimin Bi, Jiong Yan, Juliana Marcela Molina Montesdeoca, Lisa A. Yuva‐Paylor, Barbara Antalffy, Alica M. Goldman, Jong W. Yoo, Jeffrey L. Noebels, Dawna L. Armstrong, Richard Paylor, James R. Lupski	2007	65
18	Rai1 duplication causes physical and behavioral phenotypes in a mouse model of dup(17)(p11.2p11.2) Journal of Clinical Investigation ·Katherina Walz, Richard Paylor, Jiong Yan, Weimin Bi, James R. Lupski	2006	54
19	Inactivation of Rai1 in mice recapitulates phenotypes observed in chromosome engineered mouse models for Smith–Magenis syndrome Human Molecular Genetics ·Weimin Bi, Tomoko Ohyama, Hisashi Nakamura, Jiong Yan, Jaya Visvanathan, Monica J. Justice, James R. Lupski	2005	73
20	Mutations of RAI1, a PHD-containing protein, in nondeletion patients with Smith-Magenis syndrome Human Genetics ·Weimin Bi, Gulam Mustafa Saifi, Christine J. Shaw, Katherina Walz, Margareta Sjöström, Meredith Wilson, Lorraine Potocki, James R. Lupski	2004	81

About Weimin Bi

Weimin Bi is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Genetics and Cancer Research, having authored 92 papers that have together received 5.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (59 papers), Genomics and Rare Diseases (20 papers), Congenital heart defects research (18 papers), Prenatal Screening and Diagnostics (17 papers), Genetics and Neurodevelopmental Disorders (16 papers), Chromosomal and Genetic Variations (14 papers), Genomics and Chromatin Dynamics (10 papers) and Epigenetics and DNA Methylation (7 papers). The work is most often cited by research in Genetics (2.8k citations), Rheumatology (945 citations), Cancer Research (672 citations), Molecular Biology (3.0k citations) and Pediatrics, Perinatology and Child Health (719 citations). Weimin Bi has collaborated with scholars based in United States, China and United Kingdom. Frequent co-authors include Benoît De Crombrugghe, Richard R. Behringer, Zhaoping Zhang, Jian Min Deng, James R. Lupski, Sau Wai Cheung, Paweł Stankiewicz, Deanne J. Whitworth, Ankita Patel and Véronique Lefebvre. Their work appears in journals such as European Journal of Human Genetics, The American Journal of Human Genetics, Human Molecular Genetics, Prenatal Diagnosis and PLoS Genetics.

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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