Millan S. Patel

7.3k citations

54 papers · 3.9k indexed · 2 hit papers · h-index 19

Impact in

Orthopedics and Sports Medicine top 1%
- Bone health and osteoporosis research
Endocrine and Autonomic Systems top 2%
- Circadian rhythm and melatonin

Papers in

Co-authors: Gérard Karsenty Richard A. Lang Donald A. Glass Andrew P. McMahon Jong Deok Ahn Mark M. Taketo Hans Clevers Peter Bialek
Journals: Calcified Tissue International (3 papers)Scientific Reports (2 papers)The American Journal of Human Genetics (2 papers)American Journal of Medical Genetics Part A (11 papers)European Journal of Human Genetics (1 paper)
Partner nations: Canada United States United Kingdom

In The Last Decade

Millan S. Patel

50 papers receiving 3.8k citations

Hit Papers

align trajectories log scale

Canonical Wnt Signaling in Differentiated Osteoblasts Controls Osteoclast Differentiation 2005 · 1.2k citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2005 Developmental Cell
2002 The Journal of Cell Biology

Peers

Countries citing papers authored by Millan S. Patel

Since Specialization

Citations

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

Fields of papers citing papers by Millan S. Patel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Millan S. Patel. 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 Millan S. Patel. The network helps show where Millan S. Patel may publish in the future.

Co-authors

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

All Works

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20 of 20 papers shown

#	Work
1	Missense variants in homeobox domain of PBX1 cause coracoclavicular ankylosis European Journal of Human Genetics ·Maki Iwai, Kyra E. Stuurman, Kirsten Meagher, Lise Leveille, Takashi Saisu, Satomi Mori, Tatsuro Kumaki, Yumi Enomoto, Noriko Aida, Hisato Suzuki, Toshiki Takenouchi, Kenjiro Kosaki, Millan S. Patel, Kenji Kurosawa, Gen Nishimura	2025	0
2	Intraoperative Neck Angles in Endoscopic and Microscopic Otologic Surgeries Otolaryngology ·Hyonoo Joo, Zihao Lin, Lekha V. Yesantharao, Eric J. Formeister, Christopher R. Razavi, Millan S. Patel, John T. Carey, Russ Taylor, Deepa Galaiya	2023	5
3	NOTCH1 loss of the TAD and PEST domain: An antimorph? American Journal of Medical Genetics Part A ·Pierre Boerkoel, Stephanie Huynh, Gui Xiang Yang, Cornelius F. Boerkoel, Millan S. Patel, Anna Lehman, Jefferson Terry, Adrienne Elbert	2023	2
4	Comprehensive human amniotic fluid metagenomics supports the sterile womb hypothesis Scientific Reports ·HanChen Wang, Gui Xiang Yang, Yuxiang Hu, Patricia Lam, Karan Sangha, Dawn Siciliano, Anne Swenerton, Ruth R. Miller, Peter Tilley, Peter von Dadelszen, Shirin Kalyan, Patrick Tang, Millan S. Patel	2022	15
5	Somatic mosaicism detected by genome-wide sequencing in 500 parent–child trios with suspected genetic disease: clinical and genetic counseling implications Molecular Case Studies ·Courtney B. Cook, Linlea Armstrong, Cornelius F. Boerkoel, L. Clarke, Christèle du Souich, Michelle Demos, William T. Gibson, Harinder Gill, Elena Lopez‐Rangel, Millan S. Patel, Kathryn Selby, Ziad Abu-Sharar, (unknown), Alison M. Elliott, Jan M. Friedman	2021	6
6	Linkage analysis identifies an isolated strabismus locus at 14q12 overlapping with FOXG1 syndrome region Journal of Medical Genetics ·Xin Ye, Nicole M. Roslin, Andrew D. Paterson, Christopher J. Lyons, Victor Pegado, Phillip A. Richmond, Casper Shyr, Oriol Fornés, Xiaohua Han, Michelle Higginson, Colin J.D. Ross, Deborah Giaschi, Cheryl Y. Gregory‐Evans, Millan S. Patel, Wyeth W. Wasserman	2020	2
7	Congenital lactic acidosis, cerebral cysts and pulmonary hypertension in an infant with FOXRED1 related complex I deficiency Molecular Genetics and Metabolism Reports ·Delia Apatean, Bojana Rakić, Catherine Brunel‐Guitton, Glenda Hendson, Renkui Bai, Michael A. Sargent, Pascal M. Lavoie, Millan S. Patel, Sylvia Stöckler‐Ipsiroglu	2019	7
8	Competing Factors Link to Bone Health in Polycystic Ovary Syndrome: Chronic Low-Grade Inflammation Takes a Toll Scientific Reports ·Shirin Kalyan, Millan S. Patel, Elaine Kingwell, Hélène C. F. Côté, Danmei Liu, Jerilynn C. Prior	2017	35
9	Diagnosis of Van den Ende–Gupta syndrome: Approach to the Marden–Walker‐like spectrum of disorders American Journal of Medical Genetics Part A ·Karen Y. Niederhoffer, Somayyeh Fahiminiya, Patrice Eydoux, John Mawson, Gen Nishimura, Loydie A. Jerome‐Majewska, Millan S. Patel	2016	8
10	Mutations in NOTCH1 Cause Adams-Oliver Syndrome The American Journal of Human Genetics ·Anna-Barbara Stittrich, Anna Lehman, Dale L. Bodian, J. R. Ashworth, Zheyuan Zong, Hong Li, Patricia Lam, Alina Khromykh, Ramaswamy K. Iyer, Joseph G. Vockley, Rajiv Baveja, Ermelinda Santos Silva, Joanne Dixon, Eyby Leon, Benjamin D. Solomon, Gustavo Glusman, John E. Niederhuber, Jared C. Roach, Millan S. Patel	2014	136
11	A variant of unknown significance in the GLA gene causing diagnostic uncertainty in a young female with isolated hypertrophic cardiomyopathy Gene ·Khalid Al‐Thihli, Hatim Ebrahim, Derralynn Hughes, Millan S. Patel, Marion Tipple, Ramona Salvarinova, Jane Gardiner, Hilary Vallance, Paula J. Waters	2012	4
12	Outcome of prenatally diagnosed isolated clubfoot Ultrasound in Obstetrics and Gynecology ·S. Lauson, Christine M. Alvarez, Millan S. Patel, Sylvie Langlois	2010	35
13	Childhood-onset hemiatrophy caused by unilateral morphea Clinical Dysmorphology ·Anna Lehman, Millan S. Patel	2009	2
14	Sudden death in spondylo-meta-epiphyseal dysplasia, short limb-abnormal calcification type Clinical Dysmorphology ·Cristina Dias, Robyn Cairns, Millan S. Patel	2008	10
15	22q11.2 Distal Deletion: A Recurrent Genomic Disorder Distinct from DiGeorge Syndrome and Velocardiofacial Syndrome The American Journal of Human Genetics ·Shay Ben‐Shachar, Zhishuo Ou, Chad A. Shaw, John W. Belmont, Millan S. Patel, Marybeth Hummel, Stephen Amato, Nicole Tartaglia, Jonathan S. Berg, V. Reid Sutton, Seema R. Lalani, A. Craig Chinault, Sau Wai Cheung, James R. Lupski, Ankita Patel	2008	142
16	Preaxial polydactyly in neurofibromatosis 1 Clinical Dysmorphology ·Marwan Shinawi, Millan S. Patel	2007	3
17	The Molecular Clock Mediates Leptin-Regulated Bone Formation Cell ·Loning Fu, Millan S. Patel, Allan Bradley, Erwin F. Wagner, Gérard Karsenty	2005	446
18	Canonical Wnt Signaling in Differentiated Osteoblasts Controls Osteoclast Differentiation Developmental Cell ·Donald A. Glass, Peter Bialek, Jong Deok Ahn, Michael W. Starbuck, Millan S. Patel, Hans Clevers, Mark M. Taketo, Fanxin Long, Andrew P. McMahon, Richard A. Lang, Gérard Karsenty Hit paper breakdown →	2005	1234
19	Associations of the Collagen Type Iα1 Sp1 Polymorphism with Five-Year Rates of Bone Loss in Older Adults Calcified Tissue International ·Susan S. Harris, Millan S. Patel, David E.C. Cole, Bess Dawson‐Hughes	2000	41
20	Early‐infantile galactosialidosis: Prenatal presentation and postnatal follow‐up American Journal of Medical Genetics ·Millan S. Patel, John W. Callahan, Sunqu Zhang, Alicia K.J. Chan, Sheila Unger, Alex V. Levin, Marie‐Anne Skomorowski, Annette S. Feigenbaum, Karel O’Brien, Jonathan Hellmann, Greg Ryan, Lea Velsher, David Chitayat	1999	1

About Millan S. Patel

Millan S. Patel is a scholar working on Anatomy, Medical Laboratory Technology, Genetics, Pediatrics, Perinatology and Child Health and Developmental Biology, having authored 54 papers that have together received 3.9k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (4 papers), Connective tissue disorders research (4 papers), Bone health and treatments (4 papers), Wnt/β-catenin signaling in development and cancer (3 papers), Erythrocyte Function and Pathophysiology (3 papers), Neonatal Health and Biochemistry (3 papers) and Fetal and Pediatric Neurological Disorders (3 papers). The work is most often cited by research in Orthopedics and Sports Medicine (468 citations), Endocrine and Autonomic Systems (294 citations), Aging (72 citations), Molecular Biology (2.6k citations) and Genetics (802 citations). Millan S. Patel has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Gérard Karsenty, Richard A. Lang, Donald A. Glass, Andrew P. McMahon, Jong Deok Ahn, Mark M. Taketo, Hans Clevers, Peter Bialek, Michael W. Starbuck and Fanxin Long. Their work appears in journals such as Calcified Tissue International, Scientific Reports, The American Journal of Human Genetics, American Journal of Medical Genetics Part A and European Journal of Human 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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