Lynne M. Bird

8.2k total citations · 1 hit paper
101 papers, 3.2k citations indexed

About

Lynne M. Bird is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Lynne M. Bird has authored 101 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 68 papers in Genetics, 53 papers in Molecular Biology and 24 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Lynne M. Bird's work include Genetic Syndromes and Imprinting (38 papers), Epigenetics and DNA Methylation (23 papers) and Prenatal Screening and Diagnostics (20 papers). Lynne M. Bird is often cited by papers focused on Genetic Syndromes and Imprinting (38 papers), Epigenetics and DNA Methylation (23 papers) and Prenatal Screening and Diagnostics (20 papers). Lynne M. Bird collaborates with scholars based in United States, Switzerland and Canada. Lynne M. Bird's co-authors include Wen‐Hann Tan, Marilyn C. Jones, Ronald L. Thibert, Karen W. Gripp, Nicole Fleischer, Omri Bar, Yaron Gurovich, Guy Nadav, Lina Basel‐Salmon and Peter Krawitz and has published in prestigious journals such as Nature Medicine, Nature Genetics and The Journal of Experimental Medicine.

In The Last Decade

Lynne M. Bird

94 papers receiving 3.1k 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.

Identifying facial phenotypes of genetic disorders using deep learning

2018 411 citations Nicole Fleischer, Lynne M. Bird et al. profile →

Peers

Countries citing papers authored by Lynne M. Bird

Since Specialization

Citations

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

Fields of papers citing papers by Lynne M. Bird

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lynne M. Bird

This figure shows the co-authorship network connecting the top 25 collaborators of Lynne M. Bird. A scholar is included among the top collaborators of Lynne M. Bird 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 Lynne M. Bird. Lynne M. Bird 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

#	Title	Journal	Authors	Indexed citations
1	MAX‐Related Disorder: Expanding the Phenotype of the Recurrent p. Arg60Gln Variant	American Journal of Medical Genetics Part A	Nisha Shah, Lynne M. Bird et al.	0
2	Artificial Intelligence Software Changes Rare Disease Testing Strategy in Real Time: An International Case Series Using Face2Gene	American Journal of Medical Genetics Part A	Omar Abdul‐Rahman, Giulia Pascolini et al.	0
3	Intestinal Atresia in PPP1R12A ‐Related Urogenital and Brain Malformation Syndrome	American Journal of Medical Genetics Part A	Anna‐Kaisa Niemi, Lynne M. Bird et al.	0
4	Expansion of the core features of VACTERL association to include genital anomalies	American Journal of Medical Genetics Part A	Carolina I. Galarreta, Lynne M. Bird et al.	0
5	The Prevalence of RNU4-2-Associated Autosomal Dominant Intellectual Disability Syndrome	Pediatric Neurology	Jennifer Friedman, Lynne M. Bird et al.	1
6	Community‐Sourced Reporting of Mortalities in Angelman Syndrome (1979–2022)	American Journal of Medical Genetics Part A	Amanda Moore, Anne Wheeler et al.	1
7	7519 Withdrawal of DCCR (Diazoxide Choline) Extended-Release Tablets Worsens Hyperphagia and Increases Weight and BMI in a 16-week Double-blind, Placebo-controlled, Randomized Withdrawal Period in Patients with Prader Willi Syndrome	Journal of the Endocrine Society	Evelien Gevers, Jennifer Miller et al.	1
8	Substantial incidence of bladder dysfunction in patients with VACTERL association: Implications for surveillance	American Journal of Medical Genetics Part A	Carolina I. Galarreta, Lynne M. Bird et al.	1
9	Expansion of clinical and variant spectrum of EEF2‐related neurodevelopmental disorder: Report of two additional cases	American Journal of Medical Genetics Part A	Edward Cook, Cesar Alves et al.	2
10	Health-related quality of life and medication use among individuals with Angelman syndrome	Quality of Life Research	Nasreen Khan, Raquel Cabo et al.	3
11	A unique pancreatic phenotype in a child with a WDR19‐related ciliopathy: A case report and literature review of pancreatic involvement in ciliopathies	American Journal of Medical Genetics Part A	Kimberly P. Newton, Nadine Benador et al.	1
12	Haploinsufficiency of POU4F1 causes an ataxia syndrome with hypotonia and intention tremor	Human Mutation	Bryn D. Webb, Thomas P. Naidich et al.	0
13	High-voltage, diffuse delta rhythms coincide with wakeful consciousness and complexity in Angelman syndrome	Neuroscience of Consciousness	Joel Frohlich, Lynne M. Bird et al.	15
14	Angelman syndrome: Current and emerging therapies in 2016	American Journal of Medical Genetics Part C Seminars in Medical Genetics	Wen‐Hann Tan, Lynne M. Bird	42
15	Truncating mutations in the last exon of NOTCH3 cause lateral meningocele syndrome	American Journal of Medical Genetics Part A	Karen W. Gripp, Katherine Robbins et al.	59
16	If not Angelman, what is it? a review of Angelman‐like syndromes	American Journal of Medical Genetics Part A	Wen‐Hann Tan, Lynne M. Bird et al.	79
17	A Neurodevelopmental Survey of Angelman Syndrome With Genotype-Phenotype Correlations	Journal of Developmental & Behavioral Pediatrics	Jennifer Gentile, Wen‐Hann Tan et al.	117
18	Digitocutaneous dysplasia	Journal of the American Academy of Dermatology	Arash Izadpanah, Marcia Hogeling et al.	4
19	Vertically transmitted hypoplasia of the abdominal wall musculature	Clinical Dysmorphology	Lynne M. Bird et al.	11
20	Genetic mapping of X-linked loci involved in skewing of X chromosome inactivation in the human	European Journal of Human Genetics	Anna K. Naumova, Lynne M. Bird et al.	60

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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